Casiano Rivera Caroline V, Wallace Jaqulin N, Fisher Gia E, Morgan Jennifer R
Eugene Bell Center for Regenerative Biology and Tissue Engineering, Marine Biological Laboratory, Woods Hole, Massachusetts, United States.
Biological Sciences Division, The University of Chicago.
MicroPubl Biol. 2024 May 23;2024. doi: 10.17912/micropub.biology.001206. eCollection 2024.
Abnormal synaptic aggregation of α-synuclein is linked to cognitive deficits in Parkinson's disease (PD). While the impacts of excess α-synuclein on synaptic function are well established, comparatively less is known about the effects on local mitochondria. Here, we examined morphological features of synaptic mitochondria treated with wild type (WT) or phosphoserine 129 (pS129) α-synuclein, a variant with prominent synaptic accumulation in PD. Acute introduction of pS129 α-synuclein to lamprey synapses caused an activity-dependent swelling and bursting of mitochondria, which did not occur with WT α-synuclein. These pS129-induced effects on mitochondria likely contribute to the synaptic deficits observed in PD.
α-突触核蛋白的异常突触聚集与帕金森病(PD)的认知缺陷有关。虽然过量的α-突触核蛋白对突触功能的影响已得到充分证实,但对局部线粒体的影响相对了解较少。在这里,我们研究了用野生型(WT)或丝氨酸129磷酸化(pS129)α-突触核蛋白处理的突触线粒体的形态特征,pS129α-突触核蛋白是一种在PD中具有突出突触积累的变体。将pS129α-突触核蛋白急性引入七鳃鳗突触会导致线粒体的活性依赖性肿胀和破裂,而WTα-突触核蛋白则不会出现这种情况。这些pS129对线粒体的诱导作用可能导致了PD中观察到的突触缺陷。