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大鼠中磷脂酰肌醇3激酶对胞吞-转胞吞途径及胆汁分泌的调节作用

Regulation of endocytic-transcytotic pathways and bile secretion by phosphatidylinositol 3-kinase in rats.

作者信息

Folli F, Alvaro D, Gigliozzi A, Bassotti C, Kahn C R, Pontiroli A E, Capocaccia L, Jezequel A M, Benedetti A

机构信息

Department of Medicine I, H.S. Raffaele, Milano, Italy.

出版信息

Gastroenterology. 1997 Sep;113(3):954-65. doi: 10.1016/s0016-5085(97)70192-6.

Abstract

BACKGROUND & AIMS: Phosphatidylinositol 3-kinases (PI3-K) are a family of enzymes that play key roles in control of cell growth, membrane recycling, and vesicular endoexocytotic processes. The aim of this study was to investigate the effect of a specific PI3-K inhibitor, wortmannin, on bile secretion, cytoskeleton organization, and endotranscytotic pathways in rats.

METHODS

Isolated perfused rat liver (IPRL) and isolated rat hepatocyte couplets (IRHCs) were used.

RESULTS

Wortmannin induced a 25% inhibition of basal bile flow in IPRL (P < 0.01). Horseradish peroxidase biliary excretion in the IPRL was markedly decreased by wortmanin. In IRHC incubated with 25 nmol/L wortmannin for 10 minutes at 37 degrees C, morphological studies showed early significant dilatation of bite canalicular lumen (P < 0.001). At short intervals (3 minutes), uptake of the fluid-phase marker, Lucifer yellow, was markedly decreased by exposure to wortmannin (P < 0.001). At longer times (20 minutes), Lucifer yellow was retained in basolateral area of IRHC as compared with control cells, where the marker was rapidly transported to the pericanalicular area. In IRHC, wortmannin induced a marked disorganization of microfilaments.

CONCLUSIONS

Wortmannin inhibits basal bile flow, endocytosis, and transcytotic transport of fluid-phase markers in the liver, and causes an early dilatation of the canalicular lumen and disorganization of microfilaments. These findings suggest that PI3-K is involved in the regulation of vesicle trafficking, cytoskeleton organization, and the process of bile formation.

摘要

背景与目的

磷脂酰肌醇3激酶(PI3 - K)是一类在细胞生长控制、膜循环以及囊泡内吞外排过程中起关键作用的酶。本研究旨在探讨特异性PI3 - K抑制剂渥曼青霉素对大鼠胆汁分泌、细胞骨架组织及胞内膜泡运输途径的影响。

方法

采用离体灌注大鼠肝脏(IPRL)和离体大鼠肝细胞偶联物(IRHCs)。

结果

渥曼青霉素使IPRL中基础胆汁流量降低25%(P < 0.01)。渥曼青霉素显著降低了IPRL中辣根过氧化物酶的胆汁排泄。在37℃下用25 nmol/L渥曼青霉素孵育10分钟的IRHC中,形态学研究显示胆小管腔早期明显扩张(P < 0.001)。在短时间间隔(3分钟)时,暴露于渥曼青霉素会使液相标记物荧光素黄的摄取显著降低(P < 0.001)。在较长时间(20分钟)时,与对照细胞相比,荧光素黄保留在IRHC的基底外侧区域,而在对照细胞中该标记物迅速转运至胆小管周围区域。在IRHC中,渥曼青霉素导致微丝明显紊乱。

结论

渥曼青霉素抑制肝脏中的基础胆汁流量、内吞作用以及液相标记物的跨细胞运输,并导致胆小管腔早期扩张和微丝紊乱。这些发现表明PI3 - K参与囊泡运输、细胞骨架组织以及胆汁形成过程的调节。

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