| Literature DB >> 28974563 |
Eun Ju Lee1, Arif Tasleem Jan1, Mohammad Hassan Baig1, Khurshid Ahmad1, Adeel Malik2, Gulam Rabbani1, Taeyeon Kim1, In-Kyu Lee3, Yong Ho Lee4, So-Young Park5, Inho Choi1.
Abstract
Interactions between myoblasts and the surrounding microenvironment led us to explore the role of fibromodulin (FMOD), an extracellular matrix protein, in the maintenance of myoblast stemness and function. Microarray analysis of FMODkd myoblasts and in silico studies were used to identify the top most differentially expressed genes in FMODkd, and helped establish that FMOD-based regulations of integral membrane protein 2a and clusterin are essential components of the myogenic program. Studies in knockout, obese, and diabetic mouse models helped characterize the operation of a novel FMOD-based regulatory circuit that controls myoblast switching from a myogenic to a lipid accumulation fate. FMOD regulation of myoblasts is an essential part of the myogenic program, and it offers opportunities for the development of therapeutics for the treatment of different muscle diseases.-Lee, E. J., Jan, A. T., Baig, M. H., Ahmad, K., Malik, A., Rabbani, G., Kim, T., Lee, I.-K., Lee, Y. H., Park, S.-Y., Choi, I. Fibromodulin and regulation of the intricate balance between myoblast differentiation to myocytes or adipocyte-like cells.Entities:
Keywords: adipogenesis; extracellular matrix; muscle disease; myogenesis
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Year: 2018 PMID: 28974563 DOI: 10.1096/fj.201700665R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191