Monks D A, Vanston C M, Watson N V
Department of Psychology, Simon Fraser University, Burnaby, British Columbia, V5A 1S6 Canada.
J Neurosci. 1999 Jul 1;19(13):5597-601. doi: 10.1523/JNEUROSCI.19-13-05597.1999.
The spinal nucleus of the bulbocavernosus (SNB) and its target muscles, bulbocavernosus and levator ani (BC/LA), form a sexually dimorphic neuromuscular circuit whose development and maintenance are androgen-dependent. The mechanisms whereby androgen regulates gene expression in the SNB of adult rats are largely unknown, although a retrograde influence from the BC/LA muscles has been suggested to underlie the suppression of calcitonin gene-related peptide (CGRP) expression observed in SNB motoneurons after systemic androgen treatment. A mosaic paradigm was used to determine the site of action of androgen in the regulation of CGRP expression in SNB motoneurons. As a consequence of random X chromosome inactivation, androgenized female rats heterozygous for the tfm androgen receptor (AR) mutation (XwtXtfm-mosaics) express a mosaic of androgen-sensitive and androgen-insensitive motoneurons in the SNB, whereas the BC/LA target musculature appears to be uniformly sensitive to androgens. In adult mosaics, testosterone administration resulted in a reduction in the proportion of androgen-sensitive cells expressing CGRP, whereas no such reduction was observed in the androgen-insensitive population, indicating that neuronal AR plays an essential role in the neuromuscular regulation of CGRP expression in these motoneurons. This provides the first in vivo demonstration of AR regulation of gene expression unambiguously localized to a neuronal population.
球海绵体肌脊髓核(SNB)及其靶肌肉,即球海绵体肌和肛提肌(BC/LA),形成了一个具有性别差异的神经肌肉回路,其发育和维持依赖雄激素。尽管有研究表明,全身雄激素治疗后SNB运动神经元中降钙素基因相关肽(CGRP)表达受到抑制,其机制可能是BC/LA肌肉的逆行影响,但雄激素调节成年大鼠SNB中基因表达的机制仍不清楚。本研究采用镶嵌模型来确定雄激素在调节SNB运动神经元CGRP表达中的作用位点。由于随机X染色体失活,雄激素化的tfm雄激素受体(AR)突变杂合雌性大鼠(XwtXtfm镶嵌体)在SNB中表达雄激素敏感和雄激素不敏感运动神经元的镶嵌体,而BC/LA靶肌肉组织似乎对雄激素具有一致的敏感性。在成年镶嵌体中,给予睾酮导致表达CGRP的雄激素敏感细胞比例降低,而在雄激素不敏感群体中未观察到这种降低,这表明神经元AR在这些运动神经元CGRP表达的神经肌肉调节中起重要作用。这首次在体内证明了AR对基因表达的调节明确地定位于神经元群体。