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下丘脑-神经垂体神经元分泌过程的进一步研究:免疫细胞化学、麦胚凝集素-过氧化物酶及天然过氧化物酶分析

Further studies of the secretory process in hypothalamo-neurohypophysial neurons: an analysis using immunocytochemistry, wheat germ agglutinin-peroxidase, and native peroxidase.

作者信息

Broadwell R D, Cataldo A M, Balin B J

出版信息

J Comp Neurol. 1984 Sep 10;228(2):155-67. doi: 10.1002/cne.902280203.

Abstract

The axonal endoplasmic reticulum (ER) and synaptic-like (micro)vesicles within axon terminals of the neurohypophysis and their contribution to the secretory process in hypothalamo-neurohypophysial neurons have been investigated cytochemically in normal mice and in mice given 2% salt water to drink for stimulation of hormone synthesis in and release from these neurons. Cytochemical techniques included the peroxidase-antiperoxidase (PAP) immunocytochemical method for localization of neurophysin, wheat germ agglutinin-horseradish peroxidase (WGA-HRP) as a tracer for the anterograde axonal transport of membrane from within the perikaryon, and blood-borne native horseradish peroxidase (HRP) as a tracer for internalized axon terminal membrane. The primary antiserum employed was directed against neurophysins I and II, the carrier proteins for the peptide hormones oxytocin and vasopressin, respectively. PAP reaction product was observed over neurosecretory granules but never over the endoplasmic reticulum, microvesicles or other organelles in axons and terminals of the neurohypophysis. WGA-HRP was delivered extracellularly to cell bodies of paraventricular neurons by cerebral ventriculocisternal perfusion. Internalized perikaryal surface membrane tagged with WGA-HRP was recycled through the innermost Golgi saccule (GERL) from which neurosecretory granules were formed. The anterograde axonal transport of membrane-bound WGA-HRP was manifested within the neurosecretory granules; WGA-HRP did not label the axonal reticulum or terminal microvesicles in the neurohypophysis. Blood-borne native HRP endocytosed into neurohypophysial terminals was associated with a plethora of microvesicles measuring 40-70 nm in diameter and vacuoles similar in size to the 100-300-nm-wide neurosecretory granules. The microvesicles contributed to the formation of numerous vacuoles. The internalization of axon terminal membrane as microvesicles incorporating HRP was quantitatively greater than vacuoles in both salt-stressed and control mice. The results suggest that in the hypothalamo-neurohypophysial system of the mouse the axonal ER and terminal microvesicles are not involved in the transport, storage, and exocytosis of neurosecretory material and perhaps other molecules processed through the innermost Golgi saccule. Nevertheless, a prominent population of the microvesicles within axon terminals of the neurohypophysis does participate in the secretory process. These vesicles are involved directly in the internalization of the terminal surface membrane subsequent to release of secretory granule content.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

采用细胞化学方法,对正常小鼠以及饮用2%盐水以刺激下丘脑 - 神经垂体神经元激素合成与释放的小鼠,研究了神经垂体轴突终末内的轴突内质网(ER)和突触样(微)囊泡及其在这些神经元分泌过程中的作用。细胞化学技术包括:用于定位神经垂体素的过氧化物酶 - 抗过氧化物酶(PAP)免疫细胞化学方法;作为追踪剂用于顺行轴突运输核周质膜的麦胚凝集素 - 辣根过氧化物酶(WGA - HRP);以及作为追踪剂用于内化轴突终末膜的血源性天然辣根过氧化物酶(HRP)。所用的一抗分别针对神经垂体素I和II,它们分别是肽类激素催产素和加压素的载体蛋白。在神经垂体的轴突和终末中,PAP反应产物出现在神经分泌颗粒上,但从未出现在内质网、微囊泡或其他细胞器上。通过脑室池灌注将WGA - HRP细胞外递送至室旁核神经元的细胞体。标记有WGA - HRP的内化核周质表面膜通过形成神经分泌颗粒的最内层高尔基小泡(GERL)进行循环利用。膜结合的WGA - HRP的顺行轴突运输在神经分泌颗粒内表现出来;WGA - HRP未标记神经垂体的轴突内质网或终末微囊泡。血源性天然HRP被内吞入神经垂体终末后,与大量直径为40 - 70 nm的微囊泡以及大小与100 - 300 nm宽的神经分泌颗粒相似的液泡相关。这些微囊泡有助于形成大量液泡。在盐胁迫小鼠和对照小鼠中,作为结合HRP的微囊泡的轴突终末膜内化在数量上均多于液泡。结果表明,在小鼠的下丘脑 - 神经垂体系统中,轴突内质网和终末微囊泡不参与神经分泌物质以及可能通过最内层高尔基小泡加工的其他分子的运输、储存和胞吐作用。然而,神经垂体轴突终末内大量的微囊泡确实参与了分泌过程。这些囊泡在分泌颗粒内容物释放后直接参与终末表面膜的内化。(摘要截选至400字)

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