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人腹膜紧密连接、转运体和通道在健康和肾衰竭中的表达及其相关溶质转运。

Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport.

机构信息

Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.

Pediatric Center, MTA Center of Excellence, Semmelweis University, Budapest, Hungary.

出版信息

Sci Rep. 2023 Oct 13;13(1):17429. doi: 10.1038/s41598-023-44466-z.

Abstract

Next to the skin, the peritoneum is the largest human organ, essentially involved in abdominal health and disease states, but information on peritoneal paracellular tight junctions and transcellular channels and transporters relative to peritoneal transmembrane transport is scant. We studied their peritoneal localization and quantity by immunohistochemistry and confocal microscopy in health, in chronic kidney disease (CKD) and on peritoneal dialysis (PD), with the latter allowing for functional characterizations, in a total of 93 individuals (0-75 years). Claudin-1 to -5, and -15, zonula occludens-1, occludin and tricellulin, SGLT1, PiT1/SLC20A1 and ENaC were consistently detected in mesothelial and arteriolar endothelial cells, with age dependent differences for mesothelial claudin-1 and arteriolar claudin-2/3. In CKD mesothelial claudin-1 and arteriolar claudin-2 and -3 were more abundant. Peritonea from PD patients exhibited increased mesothelial and arteriolar claudin-1 and mesothelial claudin-2 abundance and reduced mesothelial and arteriolar claudin-3 and arteriolar ENaC. Transperitoneal creatinine and glucose transport correlated with pore forming arteriolar claudin-2 and mesothelial claudin-4/-15, and creatinine transport with mesothelial sodium/phosphate cotransporter PiT1/SLC20A1. In multivariable analysis, claudin-2 independently predicted the peritoneal transport rates. In conclusion, tight junction, transcellular transporter and channel proteins are consistently expressed in peritoneal mesothelial and endothelial cells with minor variations across age groups, specific modifications by CKD and PD and distinct associations with transperitoneal creatinine and glucose transport rates. The latter deserve experimental studies to demonstrate mechanistic links.Clinical Trial registration: The study was performed according to the Declaration of Helsinki and is registered at www.clinicaltrials.gov (NCT01893710).

摘要

紧邻皮肤的腹膜是人体最大的器官,主要参与腹部健康和疾病状态,但有关腹膜旁细胞紧密连接和细胞内通道及转运体相对于腹膜跨膜转运的信息却很少。我们通过免疫组织化学和共聚焦显微镜研究了其在健康、慢性肾脏病(CKD)和腹膜透析(PD)中的腹膜定位和数量,后者允许进行功能特征分析,共涉及 93 人(0-75 岁)。Claudin-1 至 -5、-15、zonula occludens-1、occludin 和 tricellulin、SGLT1、PiT1/SLC20A1 和 ENaC 均在间皮细胞和小动脉内皮细胞中被一致检测到,间皮细胞 claudin-1 和小动脉 claudin-2/3 存在年龄依赖性差异。在 CKD 中,间皮细胞 claudin-1 和小动脉 claudin-2 和 -3 更丰富。PD 患者的腹膜表现出间皮细胞和小动脉 claudin-1 以及间皮细胞 claudin-2 丰富,而间皮细胞 claudin-3 和小动脉 ENaC 减少。腹膜内肌酐和葡萄糖转运与形成孔的小动脉 claudin-2 和间皮细胞 claudin-4/-15 相关,而肌酐转运与间皮细胞钠/磷酸盐共转运体 PiT1/SLC20A1 相关。在多变量分析中,claudin-2 独立预测了腹膜转运率。总之,紧密连接、细胞内转运体和通道蛋白在腹膜间皮和内皮细胞中一致表达,在年龄组之间存在微小差异,CKD 和 PD 有特定的改变,与腹膜内肌酐和葡萄糖转运率有明显的相关性。后者值得进行实验研究以证明其机制联系。临床试验注册:该研究按照赫尔辛基宣言进行,在美国临床试验注册中心(www.clinicaltrials.gov)注册(NCT01893710)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/447c/10575882/9b2df47b2c2b/41598_2023_44466_Fig1_HTML.jpg

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