Generation of Human-Induced Pluripotent Stem Cells From Anterior Cruciate Ligament

被引:11
作者
Woods, Steven [1 ]
Bates, Nicola [1 ]
Dunn, Sara L. [2 ]
Serracino-Inglott, Ferdinand [3 ]
Hardingham, Tim E. [2 ]
Kimber, Susan J. [1 ]
机构
[1] Univ Manchester, Sch Biol Sci, Div Cell Matrix Biol & Regenerat Med, Michael Smith Bldg,Oxford Rd, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Fac Biol Med & Hlth, Wellcome Trust Ctr Cell Matrix Res, Sch Biol Sci,Div Cell Matrix Biol & Regenerat Med, Manchester, Lancs, England
[3] Cent Manchester NHS Fdn Trust, Dept Vasc Surg, Manchester, Lancs, England
基金
英国医学研究理事会;
关键词
anterior cruciate ligament; human induced pluripotent stem cells; reprogramming; ligament differentiation; tissue engineering; EPIGENETIC MEMORY; STEPWISE DIFFERENTIATION; INDUCTION; FIBROBLASTS; MATRIX; CHONDROCYTES; REPAIR;
D O I
10.1002/jor.24493
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Human-induced pluripotent stem cells (hiPSCs) are reprogrammed somatic cells and are an excellent cell source for tissue engineering applications, disease modeling, and for understanding human development. HiPSC lines have now been generated from a diverse range of somatic cell types and have been reported to retain an epigenetic memory of their somatic origin. To date, the reprogramming of a true ligament has not been reported. The aim of this study is to generate iPSCs from human anterior cruciate ligament (ACL) cells. ACL cells from three above-knee amputation donors, with donor matched dermal fibroblasts (DFs) were tested for reprogramming using an existing DF reprogramming protocol. ACL cells were, however, more sensitive than donor matched DF to transforming growth factor-beta (TGF-beta); displaying marked contraction, increased proliferation and increased TNC and COMP expression in vitro, which hindered reprogramming to iPSCs. Modification of the protocol by scoring the cell monolayer or by removal of TGF-beta during ACL reprogramming resulted in emerging colonies being easier to identify and extract, increasing reprogramming efficiency. Following 30 passages in culture, the generated ACL derived iPSCs displayed pluripotency markers, normal karyotype and can successfully differentiate to cells of the three embryonic germ layers. This study illustrates it is possible to generate hiPSCs from ligament and identifies optimized ligament reprogramming conditions. ACL derived iPSCs may provide a promising cell source for ligament and related tissue engineering applications. (c) 2019 The Authors. Journal of Orthopaedic Research (R) published by Wiley Periodicals, Inc. on behalf of Orthopaedic Research Society J Orthop Res
引用
收藏
页码:92 / 104
页数:13
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