Willeumier Kristen, Pulst Stefan M, Schweizer Felix E
Department of Neurobiology, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, California 90095, USA.
J Neurosci. 2006 Nov 1;26(44):11333-41. doi: 10.1523/JNEUROSCI.1684-06.2006.
The ubiquitin proteasome system, generally known for its function in protein degradation, also appears to play an important role in regulating membrane trafficking. A role for the proteasome in regulating presynaptic release and vesicle trafficking has been proposed for invertebrates, but it remains to be tested in mammalian presynaptic terminals. We used the fluorescent styrylpyridinium dye FM4-64 to visualize changes in the recycling pool of vesicles in hippocampal culture under pharmacological inhibition of the proteasome. We found that a 2 h inhibition increases the recycling pool of vesicles by 76%, with no change in the rate or total amount of dye release. Interestingly, enhancement did not depend on protein synthesis but did depend on synaptic activity; blocking action potentials during proteasome inhibition abolished the effect whereas increasing neuronal activity accelerated the effect with an increased recycling pool evident after 15 min. We propose that the proteasome acts as a negative-feedback regulator of synaptic transmission, possibly serving a homeostatic role.
泛素蛋白酶体系统通常以其在蛋白质降解中的功能而闻名,它似乎在调节膜运输中也起着重要作用。对于无脊椎动物,已经提出蛋白酶体在调节突触前释放和囊泡运输中发挥作用,但在哺乳动物的突触前终末中仍有待验证。我们使用荧光苯乙烯基吡啶鎓染料FM4-64来观察在蛋白酶体受到药物抑制的情况下海马培养物中囊泡循环池的变化。我们发现,2小时的抑制使囊泡循环池增加了76%,染料释放的速率或总量没有变化。有趣的是,这种增强不依赖于蛋白质合成,但依赖于突触活动;在蛋白酶体抑制期间阻断动作电位消除了这种效应,而增加神经元活动则加速了这种效应,15分钟后囊泡循环池增加明显。我们提出蛋白酶体作为突触传递的负反馈调节因子,可能起到稳态作用。