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家蚕丝素蛋白膜上角膜上皮祖细胞生长的优化

Optimization of Corneal Epithelial Progenitor Cell Growth on Bombyx mori Silk Fibroin Membranes.

作者信息

Hogerheyde Thomas A, Suzuki Shuko, Walshe Jennifer, Bray Laura J, Stephenson Sally A, Harkin Damien G, Richardson Neil A

机构信息

School of Biomedical Sciences, Faculty of Health and Institute of Health & Biomedical Innovation, Queensland University of Technology, 2 George Street, Brisbane, QLD 4001, Australia; Queensland Eye Institute, 140 Melbourne Street, South Brisbane, QLD 4101, Australia.

Queensland Eye Institute, 140 Melbourne Street, South Brisbane, QLD 4101, Australia.

出版信息

Stem Cells Int. 2016;2016:8310127. doi: 10.1155/2016/8310127. Epub 2016 Aug 28.

Abstract

Scaffolds prepared from silk fibroin derived from cocoons of the domesticated silkworm moth Bombyx mori have demonstrated potential to support the attachment and growth of human limbal epithelial (HLE) cells in vitro. In this study, we attempted to further optimize protocols to promote the expansion of HLE cells on B. mori silk fibroin- (BMSF-) based scaffolds. BMSF films were initially coated with different extracellular matrix proteins and then analysed for their impact on corneal epithelial cell adhesion, cell morphology, and culture confluency. Results showed that collagen I, collagen III, and collagen IV consistently improved HCE-T cell adherence, promoted an elongated cell morphology, and increased culture confluency. By contrast, ECM coating had no significant effect on the performance of primary HLE cells cultured on BMSF films. In the second part of this study, primary HLE cells were grown on BMSF films in the presence of medium (SHEM) supplemented with keratinocyte growth factor (KGF) and the Rho kinase inhibitor, Y-27632. The results demonstrated that SHEM medium supplemented with KGF and Y-27632 dramatically increased expression of corneal differentiation markers, keratin 3 and keratin 12, whereas expression of the progenitor marker, p63, did not appear to be significantly influenced by the choice of culture medium.

摘要

由家蚕茧中提取的丝素蛋白制备的支架已证明在体外支持人角膜缘上皮(HLE)细胞附着和生长的潜力。在本研究中,我们试图进一步优化方案以促进HLE细胞在基于家蚕丝素蛋白(BMSF)的支架上的扩增。首先用不同的细胞外基质蛋白包被BMSF膜,然后分析其对角膜上皮细胞黏附、细胞形态和培养汇合度的影响。结果表明,I型胶原、III型胶原和IV型胶原始终能改善HCE-T细胞的黏附,促进细胞形态拉长,并提高培养汇合度。相比之下,细胞外基质包被对在BMSF膜上培养的原代HLE细胞的性能没有显著影响。在本研究的第二部分,原代HLE细胞在添加角质形成细胞生长因子(KGF)和Rho激酶抑制剂Y-27632的培养基(SHEM)存在的情况下在BMSF膜上生长。结果表明,添加KGF和Y-27632的SHEM培养基显著增加了角膜分化标志物角蛋白3和角蛋白12的表达,而祖细胞标志物p63的表达似乎不受培养基选择的显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5707/5018328/c781fceb5eba/SCI2016-8310127.001.jpg

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