Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture
The isolation and propagation of primary human corneal stromal keratocytes (CSK) are crucial for cellular research and corneal tissue engineering. However, this delicate cell type easily transforms into stromal fibroblasts (SF) and scar inducing myofibroblasts (Myo-SF). Current protocols mainly rely...
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sg-ntu-dr.10356-1540132023-07-14T16:04:34Z Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture Seidelmann, Nina Duarte Campos, Daniela F. Rohde, Malena Johnen, Sandra Salla, Sabine Yam, Gary Hin-Fai Mehta, Jodhbir Singh Walter, Peter Fuest, Matthias School of Materials Science and Engineering Singapore Eye Research Institute Singapore National Eye Centre Duke-National University of Singapore Engineering::Materials Cell Culture Cornea The isolation and propagation of primary human corneal stromal keratocytes (CSK) are crucial for cellular research and corneal tissue engineering. However, this delicate cell type easily transforms into stromal fibroblasts (SF) and scar inducing myofibroblasts (Myo-SF). Current protocols mainly rely on xenogeneic fetal bovine serum (FBS). Human platelet lysate (hPL) could be a viable, potentially autologous, alternative. We found high cell survival with both supplements in CSK and SF. Cell numbers and Ki67+ ratios increased with higher fractions of hPL and FBS in CSK and SF. We detected a loss in CSK marker expression (Col8A2, ALDH3A1 and LUM) with increasing fractions of FBS and hPL in CSK and SF. The expression of the Myo-SF marker SMA increased with higher amounts of FBS but decreased with incremental hPL substitution in both cell types, implying an antifibrotic effect of hPL. Immunohistochemistry confirmed the RT-PCR findings. bFGF and HGF were only found in hPL and could be responsible for suppressing the Myo-SF conversion. Considering all findings, we propose 0.5% hPL as a suitable substitution in CSK culture, as this xeno-free component efficiently preserved CSK characteristics, with non-inferiority in terms of cell viability, cell number and proliferation in comparison to the established 0.5% FBS protocol. Published version 2022-06-07T06:01:49Z 2022-06-07T06:01:49Z 2021 Journal Article Seidelmann, N., Duarte Campos, D. F., Rohde, M., Johnen, S., Salla, S., Yam, G. H., Mehta, J. S., Walter, P. & Fuest, M. (2021). Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture. Journal of Cellular and Molecular Medicine, 25(20), 9647-9659. https://dx.doi.org/10.1111/jcmm.16912 1582-1838 https://hdl.handle.net/10356/154013 10.1111/jcmm.16912 34486211 2-s2.0-85114285559 20 25 9647 9659 en Journal of Cellular and Molecular Medicine © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. application/pdf |
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Engineering::Materials Cell Culture Cornea Seidelmann, Nina Duarte Campos, Daniela F. Rohde, Malena Johnen, Sandra Salla, Sabine Yam, Gary Hin-Fai Mehta, Jodhbir Singh Walter, Peter Fuest, Matthias Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
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The isolation and propagation of primary human corneal stromal keratocytes (CSK) are crucial for cellular research and corneal tissue engineering. However, this delicate cell type easily transforms into stromal fibroblasts (SF) and scar inducing myofibroblasts (Myo-SF). Current protocols mainly rely on xenogeneic fetal bovine serum (FBS). Human platelet lysate (hPL) could be a viable, potentially autologous, alternative. We found high cell survival with both supplements in CSK and SF. Cell numbers and Ki67+ ratios increased with higher fractions of hPL and FBS in CSK and SF. We detected a loss in CSK marker expression (Col8A2, ALDH3A1 and LUM) with increasing fractions of FBS and hPL in CSK and SF. The expression of the Myo-SF marker SMA increased with higher amounts of FBS but decreased with incremental hPL substitution in both cell types, implying an antifibrotic effect of hPL. Immunohistochemistry confirmed the RT-PCR findings. bFGF and HGF were only found in hPL and could be responsible for suppressing the Myo-SF conversion. Considering all findings, we propose 0.5% hPL as a suitable substitution in CSK culture, as this xeno-free component efficiently preserved CSK characteristics, with non-inferiority in terms of cell viability, cell number and proliferation in comparison to the established 0.5% FBS protocol. |
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School of Materials Science and Engineering |
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School of Materials Science and Engineering Seidelmann, Nina Duarte Campos, Daniela F. Rohde, Malena Johnen, Sandra Salla, Sabine Yam, Gary Hin-Fai Mehta, Jodhbir Singh Walter, Peter Fuest, Matthias |
format |
Article |
author |
Seidelmann, Nina Duarte Campos, Daniela F. Rohde, Malena Johnen, Sandra Salla, Sabine Yam, Gary Hin-Fai Mehta, Jodhbir Singh Walter, Peter Fuest, Matthias |
author_sort |
Seidelmann, Nina |
title |
Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
title_short |
Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
title_full |
Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
title_fullStr |
Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
title_full_unstemmed |
Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
title_sort |
human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture |
publishDate |
2022 |
url |
https://hdl.handle.net/10356/154013 |
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1773551239746813952 |