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Han:SPRD (cy/+)大鼠肾囊肿形成过程中的分化与细胞极性,一种常染色体显性多囊肾病模型

Differentiation and cell polarity during renal cyst formation in the Han:SPRD (cy/+) rat, a model for ADPKD.

作者信息

Obermüller N, Gretz N, Kriz W, van der Woude F J, Reilly R F, Murer H, Biber J, Witzgall R

机构信息

Medical Research Center, Klinikum Mannheim, University of Heidelberg, Germany.

出版信息

Am J Physiol. 1997 Sep;273(3 Pt 2):F357-71. doi: 10.1152/ajprenal.1997.273.3.F357.

Abstract

Despite the recent positional cloning of genes responsible for autosomal dominant polycystic kidney disease (ADPKD), the exact pathogenetic mechanisms underlying this disorder are still unclear. To learn more about cyst formation, we investigated cell differentiation and cell polarity in the Han:SPRD (cy/+) rat between 21 days and 60 wk of age. At early stages of cyst development, alkaline phosphatase, aquaporin-1, NaSi-1 cotransporter, and Na(+)-K(+)-adenosinetriphosphatase (Na(+)-K(+)-ATPase) were expressed normally. Clusterin mRNA was only sparsely expressed at the onset of cystic degeneration and increased thereafter, being highest in noncystic nephron segments. In cyst wall cells, clusterin on the one hand and alkaline phosphatase, aquaporin-1, NaSi-1-cotransporter, and Na(+)-K(+)-ATPase on the other were expressed in a mutually exclusive fashion. No change in cell polarity could be observed at any stage. Our data therefore argue against a change in cell polarity and against an early arrest in normal tubular development during cyst formation in the Han:SPRD (cy/+) rat model of ADPKD but favor the hypothesis that tubular epithelia develop in an orderly fashion and degenerate thereafter.

摘要

尽管最近已通过定位克隆技术确定了常染色体显性遗传性多囊肾病(ADPKD)相关基因,但该疾病的确切发病机制仍不清楚。为了深入了解囊肿形成过程,我们研究了21日龄至60周龄的Han:SPRD(cy/+)大鼠的细胞分化和细胞极性。在囊肿发育早期,碱性磷酸酶、水通道蛋白-1、NaSi-1协同转运蛋白和钠钾ATP酶表达正常。聚集素mRNA在囊性退变开始时仅有少量表达,随后增加,在非囊性肾单位节段中表达最高。在囊肿壁细胞中,聚集素与碱性磷酸酶、水通道蛋白-1、NaSi-1协同转运蛋白和钠钾ATP酶呈互斥性表达。在任何阶段均未观察到细胞极性改变。因此,我们的数据表明,在ADPKD的Han:SPRD(cy/+)大鼠模型中,囊肿形成过程中细胞极性未发生改变,正常肾小管发育也未早期停滞,而是支持肾小管上皮细胞有序发育而后退变的假说。

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