Baines Richard A
Neuroscience Group, Department of Biological Sciences, University of Warwick, Coventry, CV4 7AL, United Kingdom.
J Neurosci. 2004 Aug 4;24(31):6904-11. doi: 10.1523/JNEUROSCI.1978-04.2004.
Retrograde signaling is an essential component of synaptic development and physiology. Previous studies show that bone morphogenetic protein (BMP)-dependent retrograde signaling is required for the proper development of the neuromuscular junction (NMJ) in Drosophila. These studies, moreover, raised the significant possibility that the development of central motor circuitry might similarly be reliant on such signaling. To test this hypothesis, retrograde signaling between postsynaptic motoneurons and their presynaptic interneurons is examined. Postsynaptic expression of an adenylate cyclase encoded by rutabaga (rut), is sufficient to strengthen synaptic transmission at these identified central synapses. Results are presented to show that the underlying mechanism is dependent on BMP retrograde signaling. Thus, presynaptic expression of an activated TGF-beta receptor, thickvien (tkv), or postsynaptic expression of a TGF-beta ligand, glass-bottom boat (gbb), is sufficient to phenocopy strengthening of synaptic transmission. In the absence of gbb, endogenous synaptic transmission is significantly weakened and, moreover, postsynaptic overexpression of rut is unable to potentiate synaptic function. Potentiation of presynaptic neurotransmitter release, mediated by increased postsynaptic expression of gbb, is dependent on normal cholinergic activity, indicative that either the secretion of this retrograde signal, or its transduction, is activity dependent. Thus, in addition to the development of the NMJ and expression of myoactive FMRFamide-like peptides in specific central neurons, the results of the present study indicate that this retrograde signaling cascade also integrates the development and function of central motor circuitry that controls movement in Drosophila larvae.
逆行信号传导是突触发育和生理学的重要组成部分。先前的研究表明,果蝇中神经肌肉接头(NMJ)的正常发育需要骨形态发生蛋白(BMP)依赖性逆行信号传导。此外,这些研究还提出了一种极大的可能性,即中枢运动回路的发育可能同样依赖于这种信号传导。为了验证这一假设,研究人员检测了突触后运动神经元与其突触前中间神经元之间的逆行信号传导。由rutabaga(rut)编码的腺苷酸环化酶在突触后的表达足以增强这些已确定的中枢突触处的突触传递。研究结果表明,其潜在机制依赖于BMP逆行信号传导。因此,激活的转化生长因子-β受体thickvien(tkv)在突触前的表达,或转化生长因子-β配体glass-bottom boat(gbb)在突触后的表达,足以模拟突触传递的增强。在没有gbb的情况下,内源性突触传递会显著减弱,此外,rut在突触后的过表达也无法增强突触功能。由突触后gbb表达增加介导的突触前神经递质释放的增强依赖于正常的胆碱能活性,这表明这种逆行信号的分泌或其转导是依赖于活性的。因此,除了NMJ的发育以及特定中枢神经元中肌活性FMRF酰胺样肽的表达外,本研究结果表明,这种逆行信号级联还整合了果蝇幼虫中控制运动的中枢运动回路的发育和功能。