N Mizoshiri1, T Kishida2, K Yamamoto3, T Shirai4, R Terauchi4, S Tsuchida4, Y Mori1, A Ejima2, Y Sato3, Y Arai4, H Fujiwara4, T Yamamoto5, N Kanamura5, O Mazda6, T Kubo4. 1. Department of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Orthopaedics, Kyoto Prefectural University of Medicine, Kyoto, Japan. 2. Department of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan. 3. Department of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Dental Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan. 4. Department of Orthopaedics, Kyoto Prefectural University of Medicine, Kyoto, Japan. 5. Department of Dental Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan. 6. Department of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan. Electronic address: mazda@koto.kpu-m.ac.jp.
Abstract
INTRODUCTION: Osteoblasts play essential roles in bone formation and regeneration, while they have low proliferation potential. Recently we established a procedure to directly convert human fibroblasts into osteoblasts (dOBs). Transduction of Runx2 (R), Osterix (X), Oct3/4 (O) and L-myc (L) genes followed by culturing under osteogenic conditions induced normal human fibroblasts to express osteoblast-specific genes and produce calcified bone matrix both in vitro and in vivo Intriguingly, a combination of only two factors, Oct3/4 and L-myc, significantly induced osteoblast-like phenotype in fibroblasts, but the mechanisms underlying the direct conversion remains to be unveiled. MATERIALS AND METHODS: We examined which Oct family genes and Myc family genes are capable of inducing osteoblast-like phenotypic conversion. RESULTS: As result Oct3/4, Oct6 and Oct9, among other Oct family members, had the capability, while N-myc was the most effective Myc family gene. The Oct9 plus N-myc was the best combination to induce direct conversion of human fibroblasts into osteoblast-like cells. DISCUSSION: The present findings may greatly contribute to the elucidation of the roles of the Oct and Myc proteins in osteoblast direct reprogramming. The results may also lead to establishment of novel regenerative therapy for various bone resorption diseases.
INTRODUCTION: Osteoblasts play essential roles in bone formation and regeneration, while they have low proliferation potential. Recently we established a procedure to directly convert human fibroblasts into osteoblasts (dOBs). Transduction of Runx2 (R), Osterix (X), Oct3/4 (O) and L-myc (L) genes followed by culturing under osteogenic conditions induced normal human fibroblasts to express osteoblast-specific genes and produce calcified bone matrix both in vitro and in vivo Intriguingly, a combination of only two factors, Oct3/4 and L-myc, significantly induced osteoblast-like phenotype in fibroblasts, but the mechanisms underlying the direct conversion remains to be unveiled. MATERIALS AND METHODS: We examined which Oct family genes and Myc family genes are capable of inducing osteoblast-like phenotypic conversion. RESULTS: As result Oct3/4, Oct6 and Oct9, among other Oct family members, had the capability, while N-myc was the most effective Myc family gene. The Oct9 plus N-myc was the best combination to induce direct conversion of human fibroblasts into osteoblast-like cells. DISCUSSION: The present findings may greatly contribute to the elucidation of the roles of the Oct and Myc proteins in osteoblast direct reprogramming. The results may also lead to establishment of novel regenerative therapy for various bone resorption diseases.
Authors: Lauria Claeys; Nathalie Bravenboer; Elisabeth M W Eekhoff; Dimitra Micha Journal: Front Endocrinol (Lausanne) Date: 2020-06-19 Impact factor: 5.555