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Generation of hyaline cartilaginous tissue from mouse adult dermal fibroblast culture by defined factors
Kunihiko Hiramatsu, Satoru Sasagawa, Hidetatsu Outani, Kanako Nakagawa, Hideki Yoshikawa, Noriyuki Tsumaki
Kunihiko Hiramatsu, Satoru Sasagawa, Hidetatsu Outani, Kanako Nakagawa, Hideki Yoshikawa, Noriyuki Tsumaki
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Technical Advance

Generation of hyaline cartilaginous tissue from mouse adult dermal fibroblast culture by defined factors

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Abstract

Repair of cartilage injury with hyaline cartilage continues to be a challenging clinical problem. Because of the limited number of chondrocytes in vivo, coupled with in vitro de-differentiation of chondrocytes into fibrochondrocytes, which secrete type I collagen and have an altered matrix architecture and mechanical function, there is a need for a novel cell source that produces hyaline cartilage. The generation of induced pluripotent stem (iPS) cells has provided a tool for reprogramming dermal fibroblasts to an undifferentiated state by ectopic expression of reprogramming factors. Here, we show that retroviral expression of two reprogramming factors (c-Myc and Klf4) and one chondrogenic factor (SOX9) induces polygonal chondrogenic cells directly from adult dermal fibroblast cultures. Induced cells expressed marker genes for chondrocytes but not fibroblasts, i.e., the promoters of type I collagen genes were extensively methylated. Although some induced cell lines formed tumors when subcutaneously injected into nude mice, other induced cell lines generated stable homogenous hyaline cartilage–like tissue. Further, the doxycycline-inducible induction system demonstrated that induced cells are able to respond to chondrogenic medium by expressing endogenous Sox9 and maintain chondrogenic potential after substantial reduction of transgene expression. Thus, this approach could lead to the preparation of hyaline cartilage directly from skin, without generating iPS cells.

Authors

Kunihiko Hiramatsu, Satoru Sasagawa, Hidetatsu Outani, Kanako Nakagawa, Hideki Yoshikawa, Noriyuki Tsumaki

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Figure 1

Generation of the Col11a2-βgeo transgenic reporter mouse and selection of cells that acquired chondrogenic characteristics by transduction of reprogramming factors and SOX9.

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Generation of the Col11a2-βgeo transgenic reporter mouse and selection o...
(A) Schematic representation of the transgene. (B) X-gal staining of the whole body of the Col11a2-βgeo transgenic mouse at 15.5 dpc (left panel). Histological sections of primordial cartilage of the pharynx showed chondrocyte-specific LacZ activity (right panel). Scale bars: 200 μm in left panel, 100 μm in right panel. (C) MEFs prepared from Col11a2-βgeo transgenic embryos at 13.5 dpc, MDFs prepared from 6-month-old Col11a2-βgeo transgenic mice, and primary chondrocytes prepared from Col11a2-βgeo transgenic neonates and wild-type mice were cultured in the presence of various concentrations of G418. Crystal violet staining is shown. Pr Ch, primary chondrocytes. (D) Strategy to induce chondrogenic cells from MDF culture. (E) Effects of 4 reprogramming factors (4R) and/or SOX9 on the colony formation from Col11a2-βgeo reporter MDFs. Black bars indicate the number of all colonies. White bars indicate the number of colonies showing metachromatic staining with toluidine blue (*P< 0.005, compared with 4R + SOX9). Error bars indicate mean ± SD (n= 3). Col11a2-βgeo MDFs were transduced with factors indicated below the graph and selected with G418 for 2 weeks. The MOI for each vector was: pMXs-EGFP, 41; pMXs-c-Myc, 5; pMXs-Klf4, 11; pMXs-Oct3/4, 24; pMXs-Sox2, 16; pMXs-SOX9, 7.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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