Calvet J P, Grantham J J
Department of Biochemistry, Kidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
Semin Nephrol. 2001 Mar;21(2):107-23. doi: 10.1053/snep.2001.20929.
Autosomal dominant polycystic kidney disease (ADPKD) is a major, inherited disorder that is characterized by the growth of large, fluid-filled cysts from the tubules and collecting ducts of affected kidneys, and by a number of extrarenal manifestations including liver and pancreatic cysts, hypertension, heart valve defects, and cerebral and aortic aneurysms. Mutations in either of 2 different genes (PKD1 or PKD2) give rise to ADPKD. Most mutations identified in affected families appear to inactivate the PKD genes, and accumulating evidence suggests that a 2-hit mechanism, in which the normal PKD1 or PKD2 allele is also mutated, may be required for cyst growth. The protein products of the PKD genes (polycystin-1 and polycystin-2) are thought to function together as part of a multiprotein membrane-spanning complex involved in cell-cell or cell-matrix interactions. Polycystin-1 and polycystin-2 can initiate signal transduction, leading to the activation of a number of downstream effectors, including heterotrimeric G-proteins, protein kinase C, mitogen-activated protein kinases, beta-catenin, and the AP-1 transcription factor. In addition, polycystin-2 may function in mediating calcium flux. The pathogenesis of cyst formation is currently thought to involve increased cell proliferation, fluid accumulation, and basement membrane remodeling. It now appears that cyclic adenosine monophosphate (cAMP) metabolism is a central component of cyst formation, stimulating apical chloride secretion and driving the accumulation of cyst fluid. Recent evidence has shown that ADPKD cells also have an altered responsiveness to cyclic AMP. In contrast to normal kidney cells whose cell proliferation is inhibited by cyclic AMP, ADPKD cells are stimulated to proliferate. Thus, it is likely that an alteration in polycystin function transforms the normal cellular phenotype to one that responds to elevated cyclic AMP by an increased rate of cell proliferation and that the enlarging cyst expands by an increased rate of cyclic AMP-driven fluid secretion. Cyclic AMP and growth factors, including epidermal growth factor, have complementary effects to accelerate the enlargement of ADPKD cysts, and thereby to contribute to the progression of the disease. This knowledge should facilitate the discovery of inhibitors of signal transduction cascades that can be used in the treatment of ADPKD.
常染色体显性多囊肾病(ADPKD)是一种主要的遗传性疾病,其特征是患病肾脏的肾小管和集合管中形成充满液体的大囊肿,并且伴有多种肾外表现,包括肝囊肿、胰腺囊肿、高血压、心脏瓣膜缺陷以及脑动脉瘤和主动脉瘤。两种不同基因(PKD1或PKD2)中的任何一种发生突变都会导致ADPKD。在患病家族中鉴定出的大多数突变似乎会使PKD基因失活,越来越多的证据表明,囊肿生长可能需要一种双打击机制,即正常的PKD1或PKD2等位基因也发生突变。PKD基因的蛋白质产物(多囊蛋白-1和多囊蛋白-2)被认为共同发挥作用,作为参与细胞间或细胞与基质相互作用的多蛋白跨膜复合物的一部分。多囊蛋白-1和多囊蛋白-2可以启动信号转导,导致多种下游效应器的激活,包括异三聚体G蛋白、蛋白激酶C、丝裂原活化蛋白激酶、β-连环蛋白和AP-1转录因子。此外,多囊蛋白-2可能在介导钙通量中发挥作用。目前认为囊肿形成的发病机制涉及细胞增殖增加、液体蓄积和基底膜重塑。现在看来,环磷酸腺苷(cAMP)代谢是囊肿形成的核心组成部分,它刺激顶端氯化物分泌并促使囊肿液蓄积。最近的证据表明,ADPKD细胞对环磷酸腺苷的反应性也发生了改变。与正常肾细胞不同,正常肾细胞的细胞增殖受到环磷酸腺苷的抑制,而ADPKD细胞则被刺激增殖。因此,多囊蛋白功能的改变很可能将正常细胞表型转变为一种通过增加细胞增殖速率对升高的环磷酸腺苷作出反应的表型,并且不断增大的囊肿通过环磷酸腺苷驱动的液体分泌速率增加而扩大。环磷酸腺苷和生长因子,包括表皮生长因子,具有互补作用以加速ADPKD囊肿的增大,从而促进疾病的进展。这一认识应有助于发现可用于治疗ADPKD的信号转导级联抑制剂。