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用电镜放射自显影法鉴定大鼠胃中作为组胺合成内分泌细胞的肠嗜铬样(ECL)细胞。

Electron microscopic radioautographic identification of the ECL cell as the histamine-synthesizing endocrine cell in the rat stomach.

作者信息

Rubin W, Schwartz B

出版信息

Gastroenterology. 1979 Sep;77(3):458-67.

PMID:37141
Abstract

Rat gastric oxyntic glands contain argyrophil "enterochromaffin-like" endocrine cells that synthesize and store histamine and also have APUD ability--they can take up exogenous L-5-hydroxytryptophan (5-HTP), can decarboxylate it to 5-hydroxytryptamine (5-HT, serotonin) by the enzyme DOPA-decarboxylase, and can store the amine. Previous cytochemical studies suggested that these cells correspond to both the ECL and A-like cells, the two predominant endocrine cells identified by electron microscopy (EM) in rat oxyntic glands. In a recent study, however, we demonstrated that the ECL but not the A-like cell exhibited APUD ability when rat gastric mucosa was incubated with H3-5-HTP and studied by EM radioautography. The purpose of the present study was to identify by EM radioautography the histamine-synthesizing endocrine cells in the rat stomach. Pieces of rat (male Sprague-Dawley) gastric mucosa were incubated in organ culture with L-H3-histidine (50 muCi, 1.8 x 10(-5) M) with and without inhibitors and were processed for LM and EM radioautography. H3-histidine labeled the ECL cells heavily but the A-like and other endocrine cells only lightly. The labeling of ECL cells was only modestly reduced by cycloheximide, an inhibitor of protein synthesis, whereas the labeling of A-like and other endocrine cells was almost abolished. In contrast, the labeling of ECL cells was markedly reduced by 4-bromo-3-hydroxybenzyloxyamine (NSD-1055), an inhibitor of histidine decarboxylase and DOPA decarboxylase, but was not appreciably affected by carbidopa, an inhibitor of only the DOPA decarboxylase. Incubations with H3-histamine (50 muCi, 0.9 x 10(-5) M) failed to label endocrine cells. Thus, this study demonstrates that the ECL but not the A-like cell is the histamine-synthesizing endocrine cell of the rat stomach.

摘要

大鼠胃壁细胞腺含有嗜银性“肠嗜铬样”内分泌细胞,这些细胞能合成并储存组胺,且具有摄取胺前体脱羧细胞(APUD)的能力——它们能摄取外源性L - 5 - 羟色氨酸(5 - HTP),能通过多巴脱羧酶将其脱羧生成5 - 羟色胺(5 - HT,血清素),并能储存该胺类物质。先前的细胞化学研究表明,这些细胞对应于肠嗜铬样(ECL)细胞和A样细胞,这是通过电子显微镜(EM)在大鼠胃壁细胞腺中鉴定出的两种主要内分泌细胞。然而,在最近的一项研究中,我们发现当用H3 - 5 - HTP孵育大鼠胃黏膜并通过EM放射自显影术进行研究时,ECL细胞而非A样细胞表现出APUD能力。本研究的目的是通过EM放射自显影术鉴定大鼠胃中合成组胺的内分泌细胞。将大鼠(雄性斯普拉格 - 道利大鼠)胃黏膜组织块在器官培养中与L - H3 - 组氨酸(50微居里,1.8×10⁻⁵ M)一起孵育,分别添加和不添加抑制剂,然后进行光镜(LM)和EM放射自显影术处理。H3 - 组氨酸对ECL细胞标记强烈,但对A样细胞和其他内分泌细胞标记较弱。蛋白质合成抑制剂环己酰亚胺仅适度降低了ECL细胞的标记,而A样细胞和其他内分泌细胞的标记几乎完全消失。相反,组氨酸脱羧酶和多巴脱羧酶抑制剂4 - 溴 - 3 - 羟基苄氧基胺(NSD - 1055)显著降低了ECL细胞的标记,但仅多巴脱羧酶抑制剂卡比多巴对其影响不明显。用H3 - 组胺(50微居里,0.9×10⁻⁵ M)孵育未能标记内分泌细胞。因此,本研究表明,ECL细胞而非A样细胞是大鼠胃中合成组胺的内分泌细胞。

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