Igarashi M, Ohyama A, Ohbayashi K, Kozaki S, Komiya Y
Department Molecular and Cellular Neurobiology, Gunma University School of Medicine, Maebashi, Gunma, Japan.
J Neurosci Res. 2000 Jun 15;60(6):743-53. doi: 10.1002/1097-4547(20000615)60:6<743::AID-JNR6>3.0.CO;2-T.
The growth cone is considered the precursor of the presynaptic terminal. To elucidate the minimal molecular machinery required for exocytosis, we examined the characteristics of alpha-latrotoxin-induced exocytosis in growth cones. In isolated growth cones (IGC), neurotransmitters were released in a SNARE-dependent manner, but rab3A cycling was blocked. By supplying rabphilin, a rab3A acceptor found in low levels in IGC, the IGC obtained as high an exocytotic efficiency as adult synaptosomes, and the complete GDP-GTP conversion of rab3A occurred on growth cone vesicles (GCV). GCVs bound SNAREs but not NSF or alpha-SNAP; whereas in the rabphilin-supplied IGC, GCVs recruited both NSF and alpha-SNAP, to form the SNARE-NSF-SNAP complex. These results suggest that rab3A cycling is dependent upon the accumulation of rabphilin and is completed later than the SNARE mechanism, and that rabphilin is involved in determining the efficiency of exocytosis by modifying the SNARE mechanism.
生长锥被认为是突触前终末的前体。为了阐明胞吐作用所需的最小分子机制,我们研究了α-拉毒素诱导的生长锥胞吐作用的特征。在分离的生长锥(IGC)中,神经递质以SNARE依赖的方式释放,但rab3A的循环被阻断。通过提供rabphilin(一种在IGC中含量较低的rab3A受体),IGC获得了与成年突触体一样高的胞吐效率,并且rab3A在生长锥囊泡(GCV)上发生了完整的GDP-GTP转化。GCV结合SNARE,但不结合NSF或α-SNAP;而在提供了rabphilin的IGC中,GCV招募了NSF和α-SNAP,形成了SNARE-NSF-SNAP复合物。这些结果表明,rab3A的循环依赖于rabphilin的积累,并且比SNARE机制完成得晚,而且rabphilin通过修饰SNARE机制参与决定胞吐作用的效率。