Sexual dimorphism and androgen regulation of satellite cell population in differentiating rat levator ani muscle

Dev Neurobiol. 2008 Jan;68(1):115-22. doi: 10.1002/dneu.20580.

Abstract

The bulbocavernosus (BC) and levator ani (LA) muscles of rats show remarkable androgen-dependent sexual dimorphism. These muscles are additionally of interest because they are thought to indirectly mediate sexual differentiation of innervating spinal motoneurons. This sexual differentiation of the BC/LA is thought to be due to an increase in muscle units in the male rat during the first week after birth. We examined the cellular basis of this differentiation by studying satellite cells in the LA of postnatal day 2.5 rats, when sexual dimorphism is already prominent. Two experiments were performed in which LA satellite cells were measured: (1) wild-type (WT) males were compared with females and to Tfm androgen receptor mutant males, which are androgen insensitive despite producing masculine amounts of testosterone, and (2) females treated prenatally and/or postnatally with testosterone proprionate were compared with females receiving vehicle injections. Our results indicate that WT males have a larger LA and a greater number of satellite cells in the LA muscle than females or Tfm males. However, satellite cell density was similar for all three groups. Prenatal testosterone treatment masculinized LA size and resulted in a corresponding increase in satellite cell populations, while postnatal TP treatment resulted in a tendency for increased satellite cell density without a significant increase in LA size. Taken together, these studies indicate that satellite cells in the neonatal LA muscle are sexually dimorphic, and that this dimorphism likely results from perinatal actions of androgens on androgen receptors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / physiology*
  • Animals
  • Animals, Genetically Modified
  • Animals, Newborn
  • Cell Differentiation / physiology*
  • Female
  • Male
  • Muscle, Skeletal / cytology*
  • PAX7 Transcription Factor / genetics
  • PAX7 Transcription Factor / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Androgen / genetics
  • Satellite Cells, Skeletal Muscle / physiology*
  • Sex Characteristics*

Substances

  • Androgens
  • PAX7 Transcription Factor
  • PAX7 protein, human
  • Receptors, Androgen