Abdul-Majeed Shakila, Nauli Surya M
Department of Pharmacology, University of Toledo, Toledo, OH, USA.
Biochim Biophys Acta. 2011 Oct;1812(10):1281-90. doi: 10.1016/j.bbadis.2010.09.016. Epub 2010 Oct 12.
In this review, we will discuss several well-accepted signaling pathways toward calcium-mediated mechanisms of cystic expansion. The second messenger calcium ion has contributed to a vast diversity of signal transduction pathways. We will dissect calcium signaling as a possible mechanism that contributes to renal cyst formation. Because cytosolic calcium also regulates an array of signaling pathways, we will first discuss cilia-induced calcium fluxes, followed by Wnt signaling that has attributed to much-discussed planar cell polarity. We will then look at the relationship between cytosolic calcium and cAMP as one of the most important aspects of cyst progression. The signaling of cAMP on MAPK and mTOR will also be discussed. We infer that while cilia-induced calcium fluxes may be the initial signaling messenger for various cellular pathways, no single signaling mediator or pathway is implicated exclusively in the progression of the cystic expansion. This article is part of a Special Issue entitled: Polycystic Kidney Disease.
在本综述中,我们将讨论几种被广泛认可的、通向钙介导的囊性扩张机制的信号通路。第二信使钙离子参与了多种多样的信号转导通路。我们将剖析钙信号传导,将其作为一种可能导致肾囊肿形成的机制。由于胞质钙也调节一系列信号通路,我们将首先讨论纤毛诱导的钙通量,接着讨论与备受关注的平面细胞极性相关的Wnt信号通路。然后,我们将探讨胞质钙与环磷酸腺苷(cAMP)之间的关系,这是囊肿进展的最重要方面之一。我们还将讨论cAMP对丝裂原活化蛋白激酶(MAPK)和哺乳动物雷帕霉素靶蛋白(mTOR)的信号传导。我们推断,虽然纤毛诱导的钙通量可能是各种细胞通路的初始信号信使,但没有单一的信号介质或通路专门参与囊性扩张的进展。本文是名为“多囊肾病”的特刊的一部分。