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Correction to: Angiopoietin-1 receptor Tie2 distinguishes multipotent differentiation capability in bovine coccygeal nucleus pulposus cells
Stem Cell Research & Therapy volume 10, Article number: 49 (2019)
- The original article was published in Stem Cell Research & Therapy 2016 7:75
Correction to: Stem Cell Res Ther (2016) 7:75
Following publication of the original article in Stem Cell Research & Therapy , we would like to alert the reader that the immune-histological sections shown in Fig. 2 bottom line are mistakenly the images from an experiment using a different Tie2+ antibody than originally reported in the manuscript (i.e. R&D, anti-human Tie2 labeled APC, cat.No:FAB3131A, clone:83715, mouse IgG) for the florescence associated cell sorting (FACS). This antibody has been previously tested in the group of Prof. Dr. Daisuke Sakai and was performed by Ms Tomoko Nakai, Tokai University. This antibody, however, was not found to be specific for bovine Tie2+ cells. The immune-histology procedure was correctly described using the PG antibody from Millipore. However, the pictures presented in Fig. 2 in the last raw in the article of Tekari et al.  are not from the same experiment using the Tie2 antibody from Bioss, inc. clone bs-1300R, Bioss Antibodies, Woburn, MA, USA, as the publication reported.
We have now fixed this issue by providing a new Fig. 2 using the reported Tie2 primary antibody from Bioss and the secondary antibody labeled with Alexa 488 (cat# A-11008, Molecular Probes, Life Technologies, Zug, Switzerland) for FACS sorting.
The corrected Material and Methods Section for this part on page 4 of the original article should read:
“Immunohistochemical staining for proteoglycans was performed by incubation of the sections with a monoclonal mouse anti-human proteoglycan antibody (10 μg/ml, clone EFG-4; Millipore, Billerica, MA, USA, diluted 1:50) overnight at 4 °C after permeabilization with 100 % methanol for 2 min, rehydration and blocking with 10 % FBS in phosphate buffered saline (PBS) for 1 hour. Secondary antibody was then added after stringent washing for 1 hour on the next day, which was a goat anti-mouse antibody (Alexa Fluor 555 goat anti-mouse SFX-Kit IgG A-31621, Invitrogen, Fisher-Scientific, Basel, 1:200 diluted). Finally, slides were mounted in DAPI containing embedding medium (Fluoroshield™ cat# ab104139, abcam plc, Cambridge, UK). Images were then taken with a confocal laser scanning microscope at a 10x magnification and using 4x4 tile imaging (cLSM710, Carl Zeiss, Jena, Germany).”
Tekari A, Chan SC, Sakai D, Grad S, Gantenbein B. Angiopoietin-1 receptor Tie2 distinguishes multipotent differentiation capability in bovine coccygeal nucleus pulposus cells. Stem Cell Res Ther. 2016;7(1):75.
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Tekari, A., Chan, S.C.W., Sakai, D. et al. Correction to: Angiopoietin-1 receptor Tie2 distinguishes multipotent differentiation capability in bovine coccygeal nucleus pulposus cells. Stem Cell Res Ther 10, 49 (2019). https://doi.org/10.1186/s13287-019-1150-z