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大鼠小肠柱状细胞、杯状细胞和潘氏细胞中烟酰胺腺嘌呤二核苷酸磷酸酶(NADPase)活性的超微结构定位。

Ultrastructural localization of nicotinamide adenine dinucleotide phosphatase (NADPase) activity within columnar, goblet, and Paneth cells of rat small intestine.

作者信息

Parsons S M, Smith C E

出版信息

J Histochem Cytochem. 1984 Sep;32(9):989-97. doi: 10.1177/32.9.6086745.

Abstract

The distribution of nicotinamide adenine dinucleotide phosphatase (NADPase) activity was examined in epithelial cells of rat small intestine. Segments of ileum were fixed with glutaraldehyde and tissue chopper sections were incubated for up to 4 hr at pH 5.0 in cytochemical media prepared with NADP as substrate. NADPase activity was found primarily within the Golgi saccules of columnar, goblet, and Paneth cells. Columnar and goblet cells showed most of the NADPase activity within the saccules which were intermediate between the cis and trans faces of the Golgi stack. Paneth cells, however, showed the heaviest staining within saccules between the intermediate and innermost saccule at the trans aspect of the Golgi stack. Both columnar cells and Paneth cells also contained spotty, and sometimes heavy, deposits of reaction product within an occasional focal area of the GERL system and within an occasional lysosome. Control experiments indicated that the Golgi-associated NADPase activity was enhanced if cells were pretreated for about 12 hr with EGTA prior to incubation. No similar enhancement was apparent if the tissues were pretreated with DMSO. Furthermore, NADPase activity within the Golgi saccules could be inhibited completely by incubating intestinal epithelial cells with NADP in the presence of sodium fluoride or L(+)-tartrate.

摘要

研究了大鼠小肠上皮细胞中烟酰胺腺嘌呤二核苷酸磷酸酶(NADPase)活性的分布。用戊二醛固定回肠段,将组织切片机切取的切片在以NADP为底物制备的细胞化学培养基中于pH 5.0孵育长达4小时。发现NADPase活性主要存在于柱状细胞、杯状细胞和潘氏细胞的高尔基小泡内。柱状细胞和杯状细胞的NADPase活性大多位于高尔基堆顺面和反面之间的中间小泡内。然而,潘氏细胞在高尔基堆反面中间小泡和最内侧小泡之间的小泡内染色最深。柱状细胞和潘氏细胞在GERL系统的偶尔局部区域和偶尔的溶酶体内也含有斑点状、有时较浓密的反应产物沉积。对照实验表明,如果在孵育前用EGTA对细胞预处理约12小时,与高尔基体相关的NADPase活性会增强。如果用二甲基亚砜预处理组织,则没有明显的类似增强。此外,在氟化钠或L(+)-酒石酸存在的情况下,用NADP孵育肠上皮细胞可完全抑制高尔基小泡内的NADPase活性。

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