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缝隙连接蛋白 36 敲除后肠道收缩功能改变以及氮能肠神经元之间形成电突触的缝隙连接证据。

Functional alterations in gut contractility after connexin36 ablation and evidence for gap junctions forming electrical synapses between nitrergic enteric neurons.

机构信息

Department of Physiology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.

Department of Physiology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada; Department of Immunology and Internal Medicine section of Gastroenterology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.

出版信息

FEBS Lett. 2014 Apr 17;588(8):1480-90. doi: 10.1016/j.febslet.2014.02.002. Epub 2014 Feb 15.

DOI:10.1016/j.febslet.2014.02.002
PMID:24548563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4043341/
Abstract

Neurons in the enteric nervous system utilize numerous neurotransmitters to orchestrate rhythmic gut smooth muscle contractions. We examined whether electrical synapses formed by gap junctions containing connexin36 also contribute to communication between enteric neurons in mouse colon. Spontaneous contractility properties and responses to electrical field stimulation and cholinergic agonist were altered in gut from connexin36 knockout vs. wild-type mice. Immunofluorescence revealed punctate labelling of connexin36 that was localized at appositions between somata of enteric neurons immunopositive for the enzyme nitric oxide synthase. There is indication for a possible functional role of gap junctions between inhibitory nitrergic enteric neurons.

摘要

肠神经系统中的神经元利用多种神经递质来协调肠道平滑肌的有节奏收缩。我们研究了由包含连接蛋白 36 的缝隙连接形成的电突触是否也有助于小鼠结肠中的肠神经元之间的通讯。与野生型相比,缝隙连接蛋白 36 敲除小鼠的肠道自发性收缩特性以及对电刺激和胆碱能激动剂的反应发生了改变。免疫荧光显示连接蛋白 36 的点状标记,该标记定位于免疫阳性的一氧化氮合酶的肠神经元体之间的贴合处。这表明抑制性氮能肠神经元之间的缝隙连接可能具有功能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/f46f6acd861f/nihms573748f6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/f46f6acd861f/nihms573748f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/aeb272d47ca7/nihms573748f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/ac29e51124bc/nihms573748f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/0923c6bac184/nihms573748f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/575c0ab92a16/nihms573748f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/c050bb8b42c6/nihms573748f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf57/4043341/f46f6acd861f/nihms573748f6.jpg

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Morphologically mixed chemical-electrical synapses formed by primary afferents in rodent vestibular nuclei as revealed by immunofluorescence detection of connexin36 and vesicular glutamate transporter-1.免疫荧光检测连接蛋白 36 和囊泡谷氨酸转运体-1显示,在啮齿动物前庭核中初级传入纤维形成形态混合的化学-电突触。
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Connexin36 (Cx36) expression and protein detection in the mouse carotid body and myenteric plexus.在小鼠颈动脉体和肌间神经丛中连接蛋白 36(Cx36)的表达和蛋白检测。
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Evidence for connexin36 localization at hippocampal mossy fiber terminals suggesting mixed chemical/electrical transmission by granule cells.证据表明连接蛋白 36 位于海马苔藓纤维末梢,提示颗粒细胞通过混合化学/电传递。
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Endogenous cellular prion protein regulates contractility of the mouse ileum.内源性细胞朊病毒蛋白调节小鼠回肠的收缩性。
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Requirement of neuronal connexin36 in pathways mediating presynaptic inhibition of primary afferents in functionally mature mouse spinal cord.功能性成熟小鼠脊髓中初级传入纤维的突触前抑制途径中介神经元连接蛋白 36 的需求。
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