## Abstract Na^+^,K^+^‐ATPase, a basolateral transporter responsible for tubular reabsorption of Na^+^ and for providing the driving force for vectorial transport of various solutes and ions, can also act as a signal transducer in response to the interaction with steroid hormones. At nanomolar conc
Protein cytoskeleton and overexpression of Na+,K+-ATPase in opossum kidney cells
✍ Scribed by Elisabete Silva; Patrício Soares-da-Silva
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 278 KB
- Volume
- 221
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Previous studies have shown that over time in culture opossum kidney (OK) cells are endowed with increased Na^+^,K^+^‐ATPase activity and expression (Silva et al., 2006, J Membr Biol 212:163–175; Silva and Soares‐da‐Silva, 2007, Am J Physiol Regul Integr Comp Physiol 293:R1764–R1770). The present work evaluated the cytoskeleton reorganization in OK cells at passages 40 and 80 in culture and its possible relationship with membrane transport proteins and cell morphology. It is shown that OK cells with 80 passages in culture have increased size, internal complexity, and total protein expression. In OK cells with 80 passages in culture the use of in‐cell western showed that ezrin/radixin/moesin complex was increased by 20%. The most abundant ankyrin‐G isoform in OK cells with 40 passages was the ∼200/220 kDa isoform, whereas in OK cells with 80 passages the most abundant isoform was the ∼170 kDa isoform. The spectrin‐βII ∼240 kDa isoform, the predominant isoform in OK cells with 40 passages, was marginally detected in OK cells with 80 passages. Besides Na^+^,K^+^‐ATPase, GLUT2, and NHE3 expression was also significantly increased in OK cells with 80 passages. It is concluded that the prolonged cell passaging of OK cells results in an interesting and valuable experimental model to analyze the reorganization of the renal cell cytoskeleton proteins and its relationship with transporter and signaling membrane proteins. J. Cell. Physiol. 221: 318–324, 2009. © 2009 Wiley‐Liss, Inc.
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