Phillips R J, Walter G C, Wilder S L, Baronowsky E A, Powley T L
Purdue University, Department of Psychological Sciences, West Lafayette, IN 47907-2081, USA.
Neuroscience. 2008 May 15;153(3):733-50. doi: 10.1016/j.neuroscience.2008.02.074. Epub 2008 Mar 18.
The protein alpha-synuclein is implicated in the development of Parkinson's disease. The molecule forms Lewy body aggregates that are hallmarks of the disease, has been associated with the spread of neuropathology from the peripheral to the CNS, and appears to be involved with the autonomic disorders responsible for the gastrointestinal (GI) symptoms of individuals afflicted with Parkinson's. To characterize the normative expression of alpha-synuclein in the innervation of the GI tract, we examined both the postganglionic neurons and the preganglionic projections by which the disease is postulated to retrogradely invade the CNS. Specifically, in Fischer 344 and Sprague-Dawley rats, immunohistochemistry in conjunction with injections of the tracer Dextran-Texas Red was used to determine, respectively, the expression of alpha-synuclein in the myenteric plexus and in the vagal terminals. Alpha-synuclein is expressed in a subpopulation of myenteric neurons, with the proportion of positive somata increasing from the stomach (approximately 3%) through duodenum (proximal, approximately 6%; distal, approximately 13%) to jejunum (approximately 22%). Alpha-synuclein is co-expressed with the nitrergic enzyme nitric oxide synthase (NOS) or the cholinergic markers calbindin and calretinin in regionally specific patterns: approximately 90% of forestomach neurons positive for alpha-synuclein express NOS, whereas approximately 92% of corpus-antrum neurons positive for alpha-synuclein express cholinergic markers. Vagal afferent endings in the myenteric plexus and the GI smooth muscle do not express alpha-synuclein, whereas, virtually all vagal preganglionic projections to the gut express alpha-synuclein, both in axons and in terminal varicosities in apposition with myenteric neurons. Vagotomy eliminates most, but not all, alpha-synuclein-positive neurites in the plexus. Some vagal preganglionic efferents expressing alpha-synuclein form varicose terminal rings around myenteric plexus neurons that are also positive for the protein, thus providing a candidate alpha-synuclein-expressing pathway for the retrograde transport of putative Parkinson's pathogens or toxins from the ENS to the CNS.
α-突触核蛋白与帕金森病的发展有关。该分子形成路易小体聚集体,这是该疾病的标志,与神经病理学从外周向中枢神经系统的传播有关,并且似乎与导致帕金森病患者胃肠道(GI)症状的自主神经紊乱有关。为了表征α-突触核蛋白在胃肠道神经支配中的正常表达,我们检查了节后神经元和节前投射,据推测该疾病通过这些结构逆行侵入中枢神经系统。具体而言,在Fischer 344大鼠和Sprague-Dawley大鼠中,免疫组织化学结合示踪剂葡聚糖-德克萨斯红注射,分别用于确定α-突触核蛋白在肌间神经丛和迷走神经终末的表达。α-突触核蛋白在肌间神经元的一个亚群中表达,阳性胞体的比例从胃(约3%)经十二指肠(近端,约6%;远端,约13%)到空肠(约22%)逐渐增加。α-突触核蛋白与一氧化氮合酶(NOS)或胆碱能标志物钙结合蛋白和钙视网膜蛋白以区域特异性模式共表达:约90%的α-突触核蛋白阳性的前胃神经元表达NOS,而约92%的α-突触核蛋白阳性的胃体-胃窦神经元表达胆碱能标志物。肌间神经丛和胃肠道平滑肌中的迷走传入终末不表达α-突触核蛋白,而实际上,所有投射到肠道的迷走节前纤维在轴突和与肌间神经元相邻的终末膨体中均表达α-突触核蛋白。迷走神经切断术消除了神经丛中大部分但不是全部的α-突触核蛋白阳性神经突。一些表达α-突触核蛋白的迷走节前传出纤维在肌间神经丛神经元周围形成曲张终末环,这些神经元也对该蛋白呈阳性,从而为假定的帕金森病病原体或毒素从肠神经系统逆行运输到中枢神经系统提供了一条表达α-突触核蛋白的候选途径。