From: Priming approaches to improve the efficacy of mesenchymal stromal cell-based therapies
Stimuli | MSC source | Model/disease | In vitro/in vivo | Results | References |
---|---|---|---|---|---|
LL-37 | Placenta | – | In vitro | Increased migration and immunosuppressive function; increased expression of IDO, IL-10, TGF-β, IL-6, and IL-1β; increased TLR-3 levels | [154] |
S1P or LL-37 | Adipose tissue and cord blood | Pulmonary artery hypertension model | In vitro/in vivo (rats) | Increased angiogenic potential by upregulation of VEGFA, CXCR4, PDGF, HGF, and Ang-1; improved self-renewal and anti-inflammatory properties; increased density of lung blood vessels (S1P) | [155] |
LPS | Adipose tissue | Partial hepatectomy model | In vitro/in vivo (mice) | Increased IL-6, TNF-α, HGF, VEGF levels in vitro; enhanced liver regeneration and decreased IL-6 and TNF-α serum levels. | [146] |
LPS and poly(I:C) | Bone marrow | – | In vitro | Induced immunosuppressive TLR3-driven phenotype, secretion CCL10, CCL5, IL-4 and IL-10, PGE2 and IDO (Poly(I:C)); Induced pro-inflammatory TLR4-driven phenotype, secretion of IL-6 and IL-8 (LPS). | [145] |
DPS30 | Bone marrow | – | In vitro | Increased proliferation and immunosuppressive potential; increased TNF-α, IL-8, TGF-β1, VCAM, CD39, CD73 and adenosine levels. | [147] |
Curcumin | Adipose tissue (rat) | Myocardial injury model | In vitro/in vivo (rats) | Increased viability; reduced fibrosis and promoted neovascularization by upregulation of VEGF2; decreased myocardial apoptosis | [160] |
Curcumin | Bone marrow (rat) | Â | In vitro | Increased osteogenesis differentiation; upregulation of HO-1, RUNX2, and osteocalcin. | [161] |
Ang1 | Bone marrow (rat) | Acute myocardial infarction model | In vitro/in vivo (rats) | Increased cell survival due to Akt phosphorylation and increase expression of Bcl-2. | [162] |
Apelin-13 | Bone marrow (mice) | – | In vitro | Increased proliferation and decreased apoptosis; induced angiogenesis in hypoxic-ischemic condition by VEGF upregulation. | [157] |
DHT | Wharton’s jelly | – | In vitro | Increased proliferation; upregulated cell migration and pro-angiogenic factors, such as MMP-9, VEGF, and angiogenin. | [156] |
Oxytocin | Bone marrow (diabetic rat) | Myocardial infarction | In vitro/in vivo (rats) | Restored secretion of KLF2; increased angiogenesis in vitro; improved cardiac function and reduced fibrosis in vivo. | [159] |
Melatonin | Bone marrow (rat) | Osteoporosis and colitis model | In vitro/in vivo (rats) | Preserved self-renewal and differentiation capacity after long-term passaging; preserved therapeutic potential of long-term passaged MSC in bone regeneration and immunotherapy in vivo. | [153] |
Melatonin | Bone marrow (rat) | Diabetic nephropathy model | In vitro/in vivo (rats) | Increased insulin and decreased angiotensin II levels; improved kidney functions. | [151] |
Tetrandrine | Bone marrow | Ear skin inflammation model | In vitro/in vivo (mice) | Increased PGE-2 expression; decreased production of TNF-α in vivo. | [144] |
Ro-31-8425 | Bone marrow | Ear skin inflammation model | In vitro/in vivo (mice) | Increased homing ability and immunosuppressive potential in vivo through CD11a upregulation and strong adhesion to ICAM-1. | [163] |