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The effects of hepatocyte growth factor and insulin‐like growth factor‐1 on the myogenic differentiation of satellite cells in human urethral rhabdosphincter
Author(s) -
Sumino Yasuhiro,
Hanada Mari,
Hirata Yuji,
Sato Fuminori,
Mimata Hiromitsu
Publication year - 2010
Publication title -
neurourology and urodynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 90
eISSN - 1520-6777
pISSN - 0733-2467
DOI - 10.1002/nau.20748
Subject(s) - hepatocyte growth factor , myogenesis , immunocytochemistry , satellite , growth factor , transfection , cellular differentiation , cell culture , multinucleate , endocrinology , medicine , cancer research , microbiology and biotechnology , biology , myocyte , receptor , gene , biochemistry , aerospace engineering , engineering , genetics
Aims To examine the effects of hepatocyte growth factor (HGF) and insulin‐like growth factor‐1 (IGF‐1) on the myogenic differentiation of human urethral rhabdosphincter (RS) satellite cells. Methods Human RS was obtained from patients undergoing radical prostatectomy for prostate cancer. Selectively cultured RS satellite cells, transfected with temperature sensitive simian virus‐40 T antigen (ts‐SV40 Tag) to extend their lifespan, were cultured at 33°C, and then incubated at 39°C to induce myogenic differentiation. Varying concentrations of HGF and IGF‐1 were added to the differentiation medium. Inactivation of SV40 Tag and evaluations of myogenic differentiation were examined by immunocytochemistry, western blotting and real‐time RT‐PCR. Results At 39°C, ts‐SV40 Tag‐transfected RS satellite cells slowly proliferated, fused to form multinucleated myotubes, and expressed myosin heavy chain (MHC) in association with the temperature‐dependent inactivation of SV40 Tag. IGF‐1 significantly accelerated the MHC expression in a dose‐dependent fashion through activation of the PI3‐kinase pathway. Conversely, HGF did not promote MHC expression due a reduction in phosphorylation of both the MAP‐kinase and the PI3‐kinase pathways, a pattern of response different than the response of proliferating RS satellite cells to HGF. Conclusions HGF did not induce myogenic differentiation of RS satellite cells. Conversely, IGF‐1 promoted myogenic differentiation of RS satellite cells via the PI3‐K pathway likewise proliferating RS satellite cells. These findings may be useful for developing novel techniques for regenerating the human RS to treat urinary incontinence. Neurourol. Urodynam. 29:470–475, 2010. © 2009 Wiley‐Liss, Inc.