Generation of mesenchymal stromal cells from cord blood: evaluation of in vitro quality parameters prior to clinical use
© The Author(s). 2017
Received: 4 September 2016
Accepted: 21 December 2016
Published: 24 January 2017
Increasing evidence suggests the safety and efficacy of mesenchymal stromal cells (MSC) as advanced therapy medicinal products because of their immunomodulatory properties and supportive role in hematopoiesis. Although bone marrow remains the most common source for obtaining off-the-shelf MSC, cord blood (CB) represents an alternative source, which can be collected noninvasively and without major ethical concerns. However, the low estimated frequency and inconsistency of successful isolation represent open challenges for the use of CB-derived MSC in clinical trials. This study explores whether CB may represent a suitable source of MSC for clinical use and analyzes several in vitro parameters useful to better define the quality of CB-derived MSC prior to clinical application.
CB units (n = 50) selected according to quality criteria (CB volume ≥ 20 ml, time from collection ≤ 24 h) were cultured using a standardized procedure for CB-MSC generation. MSC were analyzed for their growth potential and secondary colony-forming capacity. Immunophenotype and multilineage differentiation potential of culture-expanded CB-MSC were assessed to verify MSC identity. The immunomodulatory activity at resting conditions and after inflammatory priming (IFN-γ-1b and TNF-α for 48 hours) was explored to assess the in vitro potency of CB-MSC prior to clinical application. Molecular karyotyping was used to assess the genetic stability after prolonged MSC expansion.
We were able to isolate MSC colonies from 44% of the processed units. Our results do not support a role of CB volume in determining the outcome of the cultures, in terms of both isolation and proliferative capacity of CB-MSC. Particularly, we have confirmed the existence of two different CB-MSC populations named short- and long-living (SL- and LL-) CBMSC, clearly diverging in their growth capacity and secondary colony-forming efficiency. Only LL-CBMSC were able to expand consistently and to survive for longer periods in vitro, while preserving genetic stability. Therefore, they may represent interesting candidates for therapeutic applications. We have also observed that LL-CBMSC were not equally immunosuppressive, particularly after inflammatory priming and despite upregulating priming-inducible markers.
This work supports the use of CB as a potential MSC source for clinical applications, remaining more readily available compared to conventional sources. We have provided evidence that not all LL-CBMSC are equally immunosuppressive in an inflammatory environment, suggesting the need to include the assessment of potency among the release criteria for each CB-MSC batch intended for clinical use, at least for the treatment of immune disorders as GvHD.
Mesenchymal stromal cells (MSC) comprise a heterogeneous population of multipotent progenitor cells used in clinic for their immunomodulatory properties and their supportive role in hematopoiesis. Three main criteria have been proposed by the International Society for Cellular Therapy (ISCT) for MSC definition: (1) adherence to plastic under standard culture conditions; (2) expression of CD105, CD73, CD90, and lack of expression of HLA-DR, together with the hematopoietic and endothelial surface markers CD14, CD45, CD34, CD11b, and CD31; (3) in vitro differentiation potential into osteocytes, chondrocytes, and adipocytes under appropriate culture conditions .
MSC are potent modulators of immune responses, by virtue of direct cell-cell contact and production of poorly defined soluble factors [2–4]. MSC are not constitutively inhibitory, but acquire their immunosuppressive functions following priming by inflammatory cytokines, mainly interferon gamma (IFN-γ) and tumor necrosis factor alpha (TNF-α) [5, 6]. The inducible MSC immunoregulatory properties are shared by MSC from bone marrow (BM) and other tissues, as well as by more differentiated fibroblasts .
The amenability to ex vivo expansion and the immunomodulatory activity of MSC have encouraged extensive studies paving the way for their therapeutic use, in the context of hematopoietic stem cell transplantation (HSCT) and other clinical settings [8–10]. Since 2004, the use of cryopreserved allogeneic MSC for the treatment of steroid-refractory acute graft-versus-host disease (aGvHD) has become medical practice in many countries [11, 12].
Although BM remains the most common source, MSC can be isolated from various human tissues [13–15]. Particularly, cord blood (CB) represents an alternative source, which can be collected noninvasively and without major clinical concerns. The network of public CB banks worldwide provides an easy-to-access system for the use of fresh CB units for MSC generation when they are not suitable for banking, so that CB-derived MSC can be expanded and cryopreserved in advance with enormous clinical advantages.
CB-MSC display peculiar morphological, differentiative and trophic properties [16, 17]. Some authors demonstrated a higher proliferative potential of CB-MSC compared with BM- or adipose tissue-derived MSC, together with a normal karyotype after prolonged expansion [18–20]. More recently, the existence of distinct stromal CB populations with different performances in vitro has been postulated, on the basis of their proliferative potential, colony-forming efficiency, and telomere length . Fewer studies have comprehensively addressed the immunomodulatory properties of CB-MSC, exerted on several T cell subsets and NK cells, but also through inhibition of dendritic cell function [20, 22–25].
To date, the low estimated frequency and the inconsistency of successful isolation are open challenges for the use of CB-MSC in clinical trials [26–28]. Most authors over the last years have suggested that CB volume and time from collection should be considered for a successful CB-MSC isolation [20, 29–31]. Recent studies have proposed efficient methods to obtain CB-MSC, avoiding strict quality selection of the starting material. These methods combined the traditional MNC separation or CB immunodepletion with the addition of variable supplements or coating strategies to support MSC growth [32, 33]. In this regard, the use of dexamethasone at the beginning of the culture has proven to inhibit monocyte adhesion and support CB-MSC proliferation [20, 33, 34], without inducing changes in the subsequent differentiation potential .
The present study aimed at obtaining MSC from CB, by means of an isolation procedure based on the transient use of dexamethasone as medium supplement. An essential goal was to analyze several in vitro parameters useful to define the quality of CB-derived MSC in view of their clinical use. Ultimately, the immunomodulatory function during the inflammation process was assessed as a measure of their in vitro potency, with the aim to improve cell characterization.
Cord blood collection
CB was collected after maternal informed consent from the Department of Transfusion Medicine, San Bortolo Hospital (Vicenza, Italy). CB units were collected from full-term deliveries by venipuncture immediately after cord clamping and before the delivery of placenta (in utero), then stored in bags containing 30 ml of citrate phosphate dextrose (Fresenius-Kabi, Bad Homburg vor der Höhe, Germany). Only CB units not suitable for banking with a net volume higher than 20 ml were processed within 24 hours from the collection. Clinical information from each donor including pregnancy details and CB parameters was prospectively collected.
CB-MSC isolation and expansion
Mononuclear cells (MNC) were obtained by density gradient centrifugation (Lymphoprep™, Sentinel Ch. Spa, Milan, Italy) of whole CB diluted 1:1 with phosphate-buffered saline (D-PBS, Sigma-Aldrich, St. Louis, MO, USA). MNC were collected from the interphase, washed twice with D-PBS and plated at a density of 1–2 × 106 cells/cm2 and 5–7 × 106 cells/ml in low-glucose Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 20% of fetal bovine serum (FBS) (both from Gibco, Thermo Fisher Scientific, Waltham, MA, USA), 10-7M dexamethasone (DEXA) (Hospira, Lake Forest, IL, USA), 100 U/ml penicillin and 100 μg/ml streptomycin (Sigma-Aldrich). Cells were then incubated at 37 °C in a humidified atmosphere containing 5% CO2 and standard O2 concentrations. One week from initial plating, nonadherent cells were removed. Remaining cells were fed once a week and screened for colony appearance for a maximum of 4 weeks (see Additional file 1: Fig. S1). DEXA was added in the culture until the detection of MSC colonies or alternatively supplemented for only the first week of MNC culture (n = 16 and n = 34 CB units, respectively; see Additional file 2: Fig. S2). MSC colonies at 80% confluence were harvested using 10 × TrypLE Select (Thermo Fisher Scientific) and subcultured at a density of 4000 cells/cm2. Standard medium was replaced twice a week and proliferation patterns were established by counting cells each week.
Growth kinetics and secondary colony-forming ability of CB-MSC
To estimate MSC growth, cells under maintenance conditions were progressively subcultured for 10–12 passages. At each subcultivation, the population doubling (PD) was calculated as follows: PD = log10 (N)/log10 (2), where N is the number of harvested cells/the number of initially seeded cells. The cumulative PD (cPD) was calculated adding to the PD of the passage under analysis the PDs of the previous passages.
To evaluate the secondary colony-forming ability of CB-MSC, 200 MSC collected at P1 were plated in duplicate into 100-mm diameter culture dishes (Cellstar®, Grainer Bio-One GmbH, Frickenhausen, Germany) for six to seven additional passages. Standard medium was changed weekly and after 2 weeks the cells were fixed with 10% formalin, washed with deionized water and stained with May-Grunwald-Giemsa for 20 minutes. Colonies consisting of at least 30 cells were counted under an inverted light microscope (Axiovert 40 CFL, Zeiss, Oberkochen, Germany).
Molecular karyotyping of CB-MSC (n = 3) at early (P5) and late passages (P11–13) was performed through array-comparative genomic hybridization (array-CGH) with CytoChip Oligo ISCA 4 × 180 K platform (BlueGnome, Cambridge, UK) and Fluorescent Labelling System (dUTP) kit (BlueGnome). High molecular weight DNA was extracted using the QIAamp DNA Mini kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocol. A pool of characterized genomic DNA (Human Genomic DNA Male and Female, Promega, Madison, WI, USA) was used as control DNA for all experiments. Sample and control DNA were labeled with Cy3 and Cy5 fluorophores, using random primers. Labeling mixes were combined and concentrated for hybridization. Labeled DNA was resuspended with blocking agents in hybridization buffer and applied to the CytoChip Oligo array surfaces using the gasket slides. Hybridization was performed in a rotating oven. Hybridized CytoChips were washed to remove unbound labeled DNA. A laser scanner was used to excite the hybridized fluorophores and read and store the resulting images of the hybridization. Data analysis was performed through BlueFuse Multi for Microarrays v4.0 software-cytochip V2 algorithm (Illumina, San Diego, CA, USA). Quality control parameters for every experiment were evaluated.
CB-MSC trilineage differentiation
For osteogenic and adipogenic differentiation, CB-MSC at the end of passage 4 were seeded at a density of 4000 cells/cm2 on cell culture coverslips (Thermo Fisher Scientific) arranged in 24-well plates (Falcon®, Corning, Corning, NY, USA) in the presence of standard growth medium. At 70–80% of cell confluence, the medium was replaced with specific differentiation media, then renewed every 3–4 days for 21 days. To induce adipogenic differentiation, cells were incubated using the StemPro® Adipogenic Differentiation Kit (Thermo Fisher Scientific), according to the manufacturer’s instructions. The presence of intracellular lipid droplets was detected by standard staining with Oil Red O (Diapath, Bergamo, Italy), according to the manufacturer’s instructions. In parallel, cells were also grown using the StemPro® Osteogenic Differentiation Kit (Thermo Fisher Scientific) to induce osteogenic differentiation. The presence of calcium deposits was evaluated by von Kossa staining (Sigma-Aldrich). Cells were fixed with 10% formalin for 5 minutes at room temperature, incubated with 1% silver nitrate solution for 15 minutes and exposed to ultraviolet light for 2 hours. Coverslips were rinsed with distilled water and 5% sodium thiosulfate to remove unreacted silver. Finally, cells were counterstained with Nuclear Fast Red Solution (Sigma-Aldrich). To induce chondrogenesis, 25 × 104 cells were placed in a 15-ml polypropylene tube (Falcon®, Corning) and washed in order to form a pelleted cellular micromass at the bottom of the tube. The cell pellet was cultured in 500 μl chondrogenic induction medium (StemPro® Chondrogenic Differentiation Kit, Thermo Fisher Scientific), following the recommendations of the manufacturer. Fresh chondrogenic medium was added every 3–4 days. After 28 days, the micromass was fixed, embedded in agar, cut with a microtome and stained with Alcian Blue (Sigma-Aldrich). Cells were counterstained with Nuclear Fast Red Solution.
RNA isolation and quantitative real-time polymerase chain reaction (qRT-PCR)
Total RNA was extracted using RNeasy Plus Mini Kit (Qiagen) following the manufacturer’s instructions and its quality and quantity were determined using a Nanodrop UV-VIS spectrophotometer (Thermo Fisher Scientific). First-strand cDNA were synthesized from 800 ng of total RNA in 20 μl final volume, using the iScript cDNA synthesis kit (Bio-Rad Laboratories, Hercules, CA, USA) according to the manufacturer’s instructions. The mRNA expression of osteogenic markers RUNX2 and ALP, adipogeneic markers PPARG and FABP4, and chondrogenic markers SOX9 and COLXA1 was quantified by using Sso Fast evaGreen Supermix (Bio-Rad Laboratories) on the ABI 7500 Real-Time PCR System (Applied Biosystems, Thermo Fisher Scientific), according to the producer’s recommendations. Primer sequences are summarized in Additional file 3: Table S1. The thermal cycling protocol involved initial denaturation at 95 °C for 30 sec and was followed by 40 cycles of denaturation at 95 °C for 5 sec and primer annealing and elongation for 32 sec at 60 °C, with a final melting curve analysis to test for the specificity of the product. Data acquisition and analysis were obtained by using SDS v1.4 software (Applied Biosystems, Thermo Fisher Scientific). Each gene was tested in three replicates and three independent experiments were performed. The level of each target gene was normalized to the undifferentiated control by using the 2-ΔΔCT method to quantify the relative changes in gene expression and by applying the efficiency correction represented by the equation: efficiency = 10(-1/slope) -1. TBP and YWHAZ were used as endogenous reference genes , provided the verification of their stability under differentiation conditions (Additional file 4: Fig. S3). PCR efficiency corrections were determined for target and reference genes by running a standard PCR curve using diluted cDNA.
Five color combinations of monoclonal antibodies (mAbs) were used to identify and characterize CB-MSC (n = 5) after passage 2 according to the expression of a panel of markers shown in Additional file 5: Table S2. A restricted panel was used to detect the phenotypic modifications induced on MSC by inflammatory priming (see Additional file 6: Table S3). Inflammatory priming was performed by treating CB-MSC at 80% confluence with 10 ng/ml rh-IFN-γ-1b (Imukin, Boehringer-Ingelheim, Ingelheim, Germany) and 15 ng/ml rh-TNF-α (R&D Systems, Minneapolis, MN, USA) for 48 hours of culture, as suggested by the ISCT .
About 105 cells were stained for 15 minutes at room temperature in the dark with the specific combination of mAbs. Appropriate fluorescence-minus-one (FMO) and unstained controls were used to determine the level of unspecific binding. At least 10,000 events were acquired on a Cytomics FC500 cytometer (Beckman Coulter, Brea, CA, USA). Data were analyzed by Kaluza software 2.1 version (Beckman Coulter). Expression of individual markers was recorded as the ratio of median fluorescence intensity obtained for each marker and its negative or FMO control in the corresponding fluorescence detector (rMFI).
Peripheral blood mononuclear cells (PBMC) were obtained from buffy coats of healthy donors after informed consent. PBMC were isolated by density gradient centrifugation and cryopreserved until use. Thawed PBMC were suspended in RPMI 1640 (Sigma-Aldrich) supplemented with 10% FBS, 1 × L-glutamine (Sigma-Aldrich), 100 U/ml penicillin and 100 μg/ml streptomycin and rested overnight at 37 °C in a humidified atmosphere containing 5% CO2 and standard O2 concentrations. Overnight resting allowed only a minimal monocyte adhesion, as shown in Additional file 7: Fig. S4. Resting and primed CB-MSC (n = 4), the latter stimulated for 48 hours of culture with IFN-γ-1b and TNF-α, were seeded in 96-well flat-bottomed plates (Falcon®, Corning): 4 × 104 cells for the highest (1:0.2) PBMC:MSC ratio were titrated to 1 × 104 to achieve the lowest (1:0.05) PBMC:MSC ratio.
To measure proliferation, PBMC were stained with 5 μM 5,6-carboxyfluorescein diacetate succinimidyl ester (CellTrace™ CFSE Cell Proliferation Kit, Invitrogen, Thermo Fisher Scientific) according to the manufacturer’s instructions. CFSE-labeled cells were seeded on a MSC monolayer at different PBMC:MSC ratios: 1:0.2, 1:0.1, 1:0.05 and 1:0 (no MSC treatment). Cells were stimulated with 0.5 μg/ml of anti-CD3 antibody (Miltenyi Biotec, Bergisch Gladbach, Germany) and 500 UI/ml of recombinant human interleukin-2 (rh-IL-2) (Proleukin®, Novartis, Basel, Switzerland) for 6 days before measuring the corresponding decrease in CFSE fluorescence by flow cytometry. For the latter, anti-human CD45-phycoerythrin-Texas Red (ECD) (J.33 clone, Beckman Coulter) mAb was used to assess proliferation on gated CD45+ cells. At least 50,000 events were acquired on a Cytomics FC500 cytometer. CFSE analysis was performed by Kaluza software and proliferation was quantified as the percentage of cells undergoing at least one cell division.
Clinical information and CB parameters from each donor are presented as relative frequencies or median values and their ranges for each categorical or continuous variable under study. The Kolmogorov-Smirnov and the Shapiro-Wilk tests were used to verify the normal distribution of each continuous variable. The differences between the continuous variables were computed by unpaired t test or Mann-Whitney U test as appropriate. The differences between categorical variables were computed by Fisher’s exact test. Statistical comparison between resting and primed MSC (i.e., MSC treated or not with inflammatory cytokines) for each MSC batch was performed using the t test for matched pairs. Proliferation data are presented as mean with SEM and statistical significance was calculated by two-way ANOVA. P values <0.05 were considered statistically significant. Statistical analyses were performed using GraphPad Prism 5.01 software (GraphPad Software Inc., La Jolla, CA, USA).
Comparison between donor characteristics and successful CB-MSC isolation
All samples (n = 50)
MSC-positive isolation (n = 22)
MSC-negative isolation (n = 28)
Median time after delivery, hours (range)
Median TNC × 106 (range)
Median MNC × 106 (range)
CB median volume, ml (range)
Median gestational time, days (range)
Median mother age, years (range)
Median baby weight, grams (range)
Mater/baby blood group match
Effect of dexamethasone exposure on CB-MSC culture outgrowths
As first approach we cultured 16 CB units in the presence of 10-7 M DEXA until the detection of MSC growing colonies . CB-MSC clones were isolated from 37.5% CB units (6/16). Colonies were detected at a median of 12.5 days from initial plating (range 8–20) and harvested after a median of 13.5 days (range 13–22). All samples except one reached at least five passages.
To assess whether a lower exposure to DEXA could improve CB-MSC isolation and proliferation capability, a second series of CB units (n = 34) was subjected to DEXA supplementation for the first week of MNC culture only. In this condition, MSC isolation was successful in 47.1% units (16/34), with a median detection and harvest time of 10 (range 7–15) and 12 days (range 9–15), respectively. All samples were capable to reach at least five passages.
CB-MSC growth characteristics
Differences in the proliferative capacity and exhaustion passage were observed between MSC from different units. Overall, 1/3 of CB-derived MSC were able to expand for more than nine passages. By evaluating the long-term proliferative potential at least two growth kinetics patterns were recognized. We distinguished short- and long-living (SL- and LL-) CB-MSC based on their lower or higher cPD, respectively (cPD cutoff = 20 at p9). LL-CBMSC displayed a constant greater growth and longevity than SL-CB-MSC (Fig. 2d). Moreover, by comparing the cPD at each passage, significant differences in the proliferative capacity were revealed by passage 5 (Fig. 2e).
Since the discrimination between SL- and LL-CBMSC based on the cPD could only be done retrospectively, we sought to identify an earlier distinctive marker, possibly of clinical utility for the choice of the batches of CB-MSC suitable for large-scale expansion and clinical use. As already demonstrated, the heterogeneous proliferative potential reflected differences in the self-renewal capacity [21, 38]. By assessing the secondary colony-forming capability of the two populations, we found that LL-CBMSC retained greater secondary colony-forming ability compared to SL-CBMSC. Conversely, SL-CBMSC failed to self-renew after a few passages then lost the growth capacity earlier (Fig. 2f-g). Significant differences were specifically observed at passage 4, albeit on a limited number of samples (Fig. 2h).
We next addressed the role of donor characteristics and CB parameters (listed in Table 1) as discriminating markers between LL- and SL-CBMSC. Quite surprisingly, we found that the median of CB volumes of units giving rise to SL-CBMSC was significantly higher (51 ml, range 22–87) with respect to the volume of CB units giving rise to LL-CBMSC (31 ml, range 27–42) (p = 0.0388, n = 16 and n = 5, respectively, Fig. 2i).
Finally, in order to test the genetic stability of CB-MSC after prolonged expansion, three LL-CBMSC batches at early (P5) and late passages (P11–13) were tested for their genomic assets through array-CGH analysis. Results revealed that expanded CB-MSC did not show unbalanced chromosomal rearrangements (deletion or duplication), excluding copy number variation constitutionally present (see Additional file 8: Fig. S5).
To confirm multilineage differentiation at a molecular level, the transcript levels of both early- and late-stage markers of adipogenesis, osteogenesis, and chondrogenesis were determined by means of qRT-PCR in LL-CBMSC. Results from three independent experiments confirmed, even with variability between MSC donors, significant upregulation of all mRNA transcripts involved in chondrogenic and osteogenic MSC differentiation (p = 0.0039 for SOX9, RUNX2, and ALP; p = 0.0078 for COLXA1), while the absence of significant differences for the adipogenic markers PPARG and FABP4 (p = 0.0547) (Fig. 3i-j).
We then evaluated the modifications of MSC immunophenotype after treatment with IFN-γ-1b and TNF-α for 48 hours, corresponding to induction of immunosuppressive function in MSC . As previously demonstrated, the expression of HLA-ABC, HLA-DR, CD54 (ICAM-1), and CD106 (VCAM-1) was modulated in the presence of inflammatory priming . Particularly, significant upregulation was observed for CD54 (low-negative at resting conditions) and HLA-ABC (high-positive at resting conditions) (p = 0.004 and p < 0.001, respectively, Fig. 4 c-d). Upregulation of CD106 (low-negative at resting conditions) did not reach significance, while the expression of HLA-DR (negative in resting MSC) was almost unchanged (Fig. 4b-e).
Immunosuppressive properties of CB-MSC
Obtaining definitive data on the effectiveness of MSC in the clinic is hampered by the lack of standardized protocols used to prepare large-scale MSC and of useful tests to compare their potency. Particularly, differences in donor source, culture methods, and expansion levels are critical in determining MSC functionality [41, 42].
Our study investigated whether CB may represent a suitable source of MSC for cell-based therapeutic strategies. Furthermore, the biological and functional properties of CB-derived MSC were assessed in view of a more effective and safer clinical use. By applying quality criteria for an optimal CB-MSC isolation (CB volume ≥ 20 ml, time from collection ≤ 24 h), we were able to isolate MSC colonies from 44% of processed units. We next evaluated whether isolation was influenced by any clinical features of the donors or CB parameters, but we found no correlation between the analyzed parameters and the rate of success in isolating CB-MSC. Other studies reported isolation yields ranging from fewer than 10% to 90%, revealing a lack of consensus in the methodological approaches and selection criteria for CB units [20, 21, 29, 30, 43]. By using DEXA (10-7 M) as medium supplement in addition to 20% FBS for 1 week, Zhang et al. achieved a 90% rate of success in isolating CB-MSC when the volume was ≥ 90 ml and the time to processing ≤ 2 h . By applying the same criteria, Pievani et al. were able to obtain MSC from 40% of processed units only .
DEXA was found to inhibit monocyte adhesion, thus it is conceivable a role of the steroid in supporting the proliferation of CB-MSC progenitors at the expense of other contaminants which can adhere on culture plates. Therefore, its supplementation was applied also in our study with the aim to promote the adhesion of the rare CB-MSC progenitors to the plastic. Moreover, Zhang and co-workers found no benefit from using alternative isolation methods or culture conditions, such as immunodepletion before MNC plating, addition of growth factors to the standard MSC medium, culture in hypoxia, or coating strategies . Even though the use of DEXA has been described in the generation of CB-MSC [20, 34, 35], its dosage varied between investigators. In the first isolation protocol published by Kögler et al. , DEXA (10-7 M) was added until the detection of MSC growing colonies, while the expansion was performed in the absence or at a low concentration of the supplement. In the present study, the choice to evaluate two treatment regimens with DEXA was of particular significance in order to define a standardized protocol for generating CB-MSC for clinical use. Our results showed that the extent of DEXA supplementation did not significantly affect CB culture outcomes, in regard to both isolation efficiency and long-term proliferation, even if there seemed to be better outcomes in the group of units treated with DEXA for only 1 week. Given that culture conditions may have remarkable effects on the functionality of MSC [33, 44], the addition of uncommon supplements to standard MSC medium, like hormones, should be avoided or minimized, at least when the purpose is to produce MSC with unaltered stemness properties for clinical use. It should be therefore more appropriate and equally effective keeping cell exposure to DEXA to the minimum required for an effective CB-MSC isolation.
As discussed, there are some drawbacks linked to the successful isolation and expansion of CB-MSC, mainly due to the low frequency of MSC clones in particular when compared with umbilical cord (UC), a rich source of high-proliferative MSC characterized by isolation yields of 100% . To the other hand, UC is a heterogeneous tissue whose processing is time-consuming and labor-intensive in respect to the easier manipulation of CB. Moreover, public CB banks provide an easy-to-access system for using freshly donated CB units for MSC generation, while a similar collection network system does not exist for UC or other fetal sources like placenta. The present study has also revealed that the role of volume as selection criterion for CB units processed for CB-MSC isolation should be re-considered because of affecting neither the rate of successful MSC isolation nor the growth potential. This finding would allow to use even CB units of low volume for MSC isolation.
An important outcome of the present study was to analyze several in vitro parameters that may help to better define the “quality” of CB-derived MSC prior to their clinical application. The evaluation of the proliferation capacity as first indicator of MSC potential allowed us to corroborate the findings from Barilani and co-authors , who demonstrated the existence of at least two stromal populations within CB, one long-living (LL-CBMSC) and the other short-living (SL-CBMSC) on the basis of their proliferative ability, secondary colony-forming efficiency and most importantly, telomere length. The same authors found LL-CBMSC mostly indiscernible from the SL counterpart in regard to ISCT criteria . We confirmed that the two MSC populations clearly diverge in their growth capacity and secondary colony-forming efficiency, thus suggesting a potential role of these in vitro parameters as indicators of CB-MSC longevity. On one hand, the possibility of cryopreserving low-passage CB-MSC batches in advance in respect to the clinical needs should allow to monitor cell growth until the established cPD cutoff, thus rendering the retrospective discrimination between LL- and SL-CBMSC clinically useful. On the other hand, the evaluation of secondary colony formation may be a promising and likely early parameter of longevity.
Our data confirmed the absence of major dissimilarities concerning immunophenotype and multilineage differentiation, fitting both populations the minimal panel proposed for MSC definition . It is conceivable that LL-CBMSC represent better candidates for obtaining clinically relevant numbers of MSC for therapeutic applications, due to the higher ex vivo expansion and the ability to survive for longer periods in vitro. Therefore, the assessment of their genetic stability after prolonged culture represents an important release criterion for a safe clinical use, even if overly expansion should be avoided too [46, 47].
Unlike MSC from other sources, is widely reported the relatively low adipogenesis ability of CB-MSC under standard induction protocols [48–50], most likely due to their more primordial, fetal origin in respect to other MSC sources . On the other hand, it is well documented that there is more propensity toward chondrogenesis and osteogenesis in vitro under appropriate culture conditions and to some extent in vivo [20, 35, 52, 53]. Sacchetti and co-workers  have recently demonstrated a unique capacity of CB-derived stromal cells to form cartilage in vivo spontaneously, in addition to an osteogenic capacity. Therefore, they support the presence within CB of chondro-osteoprogenitors rather than multipotent MSC, whose origin, however, remains to be elucidated. Our data confirmed an impaired adipogenic potential of CB-MSC, revealed by a clear absence of cells forming lipid droplets and confirmed at a molecular level by the absence of significant mRNA induction of PPARG and FABP4, the former representing a crucial player during the transcriptional cascade leading to adipogenic differentiation, the latter being its direct target. More in general, our molecular analysis highlighted a wide variability in the differentiation potential between individual samples. This finding may fit the increasing evidence of the existence of distinct CB-derived stromal progenitors, possibly of different developmental origin and related plasticity [53–56]. In this regard, unrestricted somatic stromal cells (USSC) and cord blood-derived stromal cells (CB-MSC) were originally defined according to the expression of the adipogenic inhibitor delta-like 1 (DLK-1), a specific marker of USSC correlating with a lack of adipogenic differentiation ability and a higher proliferative potential compared to the more differentiated and less proliferative CB-MSC . Even if in our experience a lack of adipogenic potential was common to both LL- and SL-CBMSC, it remains unclear whether the more immature USSC match our LL-CBMSC.
The ultimate aim of the present work was to investigate the immunosuppressive activity of both resting and inflammatory-primed CB-MSC, in order to complete their functional characterization prior to clinical application. Despite the recent suggestions provided by ISCT [37, 42, 57], a universally accepted in vitro method to assess MSC immunosuppression does not exist [58, 59]. We used unselected and opportunely stimulated PBMC because more closely mimic the in vivo inflammatory environment to which MSC are exposed on patient administration. Our results showed that CB-MSC inhibited PBMC proliferation with different efficacy, particularly after treatment with exogenous IFN-γ-1b and TNF-α. The lack of efficacy of one batch was found despite the flow cytometry upregulation of priming-inducible markers. Moreover, it was confirmed repeatedly on different PBMC donors. In this situation, a trophic effect mediated by primed CB-MSC was conceivable on PBMC proliferation. Additional studies would be warranted to determine how correlating this observation with other immunomodulatory markers, for adequately predicting the in vivo potency of CB-MSC. von Bahr and co-authors  reported no evidence of correlation between the in vitro inhibitory potential of MSC and in vivo clinical response in patients with aGvHD, suggesting that the in vivo efficacy of MSC not only depends on the intrinsic properties of the MSC preparation but also on the product-host interaction. A detailed immunomonitoring of patients as well as an in-depth characterization of MSC would therefore be helpful to correlate the in vitro measure of the potency with clinical outcomes .
In summary, the present work shows that CB may be a practical source of MSC for clinical applications. CB remains much more readily available and devoid of major ethical concerns in respect to other conventional MSC sources. To the best of our knowledge, we have provided evidence that not all LL-CBMSC are equally immunosuppressive in an inflammatory environment, in support of the need to include the assessment of in vitro potency among the release criteria for each CB-MSC batch intended for clinical use, at least for the treatment of immune disorders such as GvHD.
acute graft-versus-host disease
carboxyfluorescein diacetate succinimidyl ester
comparative genomic hybridization
cumulative population doublings
Dulbecco’s modified Eagle’s medium
fetal bovine serum
hematopoietic stem cell transplantation
International Society for Cellular Therapy
long-living cord blood mesenchymal stromal cells
mesenchymal stromal cells
peripheral blood mononuclear cells
quantitative real-time polymerase chain reaction
recombinant human interleukin-2
relative median fluorescence intensity
short-living cord blood mesenchymal stromal cells
total nucleated cells
tumor necrosis factor alpha
unrestricted somatic stromal cells
We are grateful to all the mothers who gave their consent to donation. We are indebted to Anna Montaldi and Paola Celli for their important intellectual contribution to genetic data discussion. We really appreciated the contribution of Cinzia Tagliaferri and Monica Mantia to cord blood collection. We would like to thank Emanuele SG D’Amore and all the technicians of the Anatomy and Histology Department of S. Bortolo Hospital (Vicenza, Italy) for their technical assistance during the staining procedures. We are grateful to Paul Takam Kamga for critical review of the manuscript and to Carmine Carbone for his valuable contribution to molecular data analysis.
This work was partially supported by grants obtained from Cariverona Foundation (Research Project 2012.0828) and from Ricerca Sanitaria Finalizzata Regionale del Veneto 2012 (Research Project 334/12), assigned to Prof. Mauro Krampera, University of Verona (Italy).
EA and SS carried out the experimental design and analyzed/interpreted results. EA designed the research and wrote the manuscript. OP was involved in data interpretation, figure preparation, manuscript drafting and critical revisions for important intellectual content. MB, KC and DP provided technical assistance and participated in sample processing. CL was involved in sample collection and provided clinical parameters of CB donors. AZ performed molecular karyotyping and analysis of Additional file 8: Figure S5. AA, MR, FR and MR critically reviewed the manuscript. GA was involved in conception and design, coordination of the study, critical revisions for important intellectual content and manuscript final approval. All authors read and approved the manuscript for publication.
The authors declare that they have no competing interests.
Consent for publication
Informed consent included the consent for publication.
Ethics approval and consent to participate
The present study was approved (reference protocol SIT-VR 13/73) and informed consent to cord blood collection and donation for research was received from the mothers (specific section in the form IBMDR SCO101, version 2, 1–3 Jan 2013).
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