Rassendren F A, Bloch-Gallego E, Tanaka H, Henderson C E
Centre de Recherche de Biochimie Macromoléculaire, UPR 8402, Centre National de la Recherche Scientifique/Institut National de la Santé et de la Recherche Médicale U249, Montpellier, France.
Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):7194-8. doi: 10.1073/pnas.89.15.7194.
Partial denervation of skeletal muscle induces sprouting of axons remaining within the muscle, possibly as a result of increased synthesis by denervated muscle fibers of motoneuron growth-promoting factors. Direct verification of this hypothesis has not been possible because the molecules responsible are not unambiguously characterized. We used Xenopus oocytes as a functional assay for mRNAs coding for secreted growth factors: preparations of mRNA from innervated and denervated neonatal muscle were injected into oocytes. Three days later, oocytes injected with denervated muscle mRNA expressed increased levels of nicotinic acetylcholine receptor and voltage-dependent sodium channels at their membrane. Proteins secreted by the same oocytes were tested for their effects on (i) neurite outgrowth from embryonic chicken ventral spinal cord neurons; (ii) survival in mixed culture of embryonic chicken motoneurons identified using the SC1 antibody; and (iii) survival of embryonic motoneurons purified by panning on SC1 antibody. In all three assays, media conditioned by oocytes injected with mRNA from denervated muscle contained significantly higher levels of biological activity than did those from oocytes injected with innervated muscle mRNA or water. mRNA was prepared from muscle at different times after denervation: a maximal increase was obtained already after 1 day, consistent with an involvement in sprouting. Synthesis of motoneuron growth-promoting factors is thus regulated by denervation in a parallel fashion to that of other key components of the neuromuscular junction.
骨骼肌的部分去神经支配会诱导留存于肌肉内的轴突发芽,这可能是由于失神经支配的肌纤维合成运动神经元生长促进因子增加所致。由于负责的分子尚未得到明确表征,因此无法直接验证这一假设。我们使用非洲爪蟾卵母细胞作为分泌性生长因子编码mRNA的功能检测方法:将来自正常支配和去神经支配的新生肌肉的mRNA制剂注射到卵母细胞中。三天后,注射了去神经支配肌肉mRNA的卵母细胞在其细胞膜上表达出更高水平的烟碱型乙酰胆碱受体和电压依赖性钠通道。对同一批卵母细胞分泌的蛋白质进行了以下测试:(i)对来自胚胎鸡腹侧脊髓神经元的神经突生长的影响;(ii)对使用SC1抗体鉴定的胚胎鸡运动神经元在混合培养中的存活情况的影响;(iii)对通过在SC1抗体上淘选纯化的胚胎运动神经元存活情况的影响。在所有这三种检测中,注射了去神经支配肌肉mRNA的卵母细胞所分泌的培养基中的生物活性水平显著高于注射了正常支配肌肉mRNA或水的卵母细胞所分泌的培养基。在去神经支配后的不同时间从肌肉中制备mRNA:在1天后就已获得最大增幅,这与参与发芽过程一致。因此,运动神经元生长促进因子的合成与神经肌肉接头的其他关键成分一样,受到去神经支配的平行调节。