Nonmyocytic androgen receptor regulates the sexually dimorphic development of the embryonic bulbocavernosus muscle
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 ES016597
NIEHS NIH HHS - United States
R01ES016597
NIEHS NIH HHS - United States
PubMed
24742196
PubMed Central
PMC4060183
DOI
10.1210/en.2014-1008
Knihovny.cz E-resources
- MeSH
- Receptors, Androgen genetics metabolism MeSH
- Time Factors MeSH
- Embryo, Mammalian embryology metabolism MeSH
- Immunohistochemistry MeSH
- Cyclin-Dependent Kinase Inhibitor p21 metabolism MeSH
- Microscopy, Electron, Scanning MeSH
- Mutation MeSH
- Myoblasts cytology metabolism MeSH
- Mice, Inbred ICR MeSH
- Mice, Knockout MeSH
- Mice, Transgenic MeSH
- Mice MeSH
- Perineum embryology MeSH
- Cell Proliferation MeSH
- Sex Factors MeSH
- Muscles embryology metabolism ultrastructure MeSH
- Pregnancy MeSH
- Transcription Factors genetics metabolism MeSH
- Muscle Development genetics physiology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- Receptors, Androgen MeSH
- Cyclin-Dependent Kinase Inhibitor p21 MeSH
- Sall1 protein, mouse MeSH Browser
- Transcription Factors MeSH
The bulbocavernosus (BC) is a sexually dimorphic muscle observed only in males. Androgen receptor knockout mouse studies show the loss of BC formation. This suggests that androgen signaling plays a vital role in its development. Androgen has been known to induce muscle hypertrophy through satellite cell activation and myonuclei accretion during muscle regeneration and growth. Whether the same mechanism is present during embryonic development is not yet elucidated. To identify the mechanism of sexual dimorphism during BC development, the timing of morphological differences was first established. It was revealed that the BC was morphologically different between male and female mice at embryonic day (E) 16.5. Differences in the myogenic process were detected at E15.5. The male BC possesses a higher number of proliferating undifferentiated myoblasts. To identify the role of androgen signaling in this process, muscle-specific androgen receptor (AR) mutation was introduced, which resulted in no observable phenotypes. Hence, the expression of AR in the BC was examined and found that the AR did not colocalize with any muscle markers such as Myogenic differentiation 1, Myogenin, and paired box transcription factor 7. It was revealed that the mesenchyme surrounding the BC expressed AR and the BC started to express AR at E15.5. AR mutation on the nonmyocytic cells using spalt-like transcription factor 1 (Sall1) Cre driver mouse was performed, which resulted in defective BC formation. It was revealed that the number of proliferating undifferentiated myoblasts was reduced in the Sall1 Cre:AR(L-/Y) mutant embryos, and the adult mutants were devoid of BC. The transition of myoblasts from proliferation to differentiation is mediated by cyclin-dependent kinase inhibitors. An increased expression of p21 was observed in the BC myoblast of the Sall1 Cre:AR(L-/Y) mutant and wild-type female. Altogether this study suggests that the nonmyocytic AR may paracrinely regulate the proliferation of myoblast possibly through inhibiting p21 expression in myoblasts of the BC.
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