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PTH-induced internalization of apical membrane NaPi2a: role of actin and myosin VI.
Blaine, Judith; Okamura, Kayo; Giral, Hector; Breusegem, Sophia; Caldas, Yupanqui; Millard, Andrew; Barry, Nicholas; Levi, Moshe.
Affiliation
  • Blaine J; Department of Medicine, University of Colorado Denver, Aurora, 80045, USA. Judith.Blaine@ucdenver.edu
Am J Physiol Cell Physiol ; 297(6): C1339-46, 2009 Dec.
Article in En | MEDLINE | ID: mdl-19776390
ABSTRACT
Parathyroid hormone (PTH) plays a critical role in the regulation of renal phosphorous homeostasis by altering the levels of the sodium-phosphate cotransporter NaPi2a in the brush border membrane (BBM) of renal proximal tubular cells. While details of the molecular events of PTH-induced internalization of NaPi2a are emerging, the precise events governing NaPi2a removal from brush border microvilli in response to PTH remain to be fully determined. Here we use a novel application of total internal reflection fluorescence microscopy to examine how PTH induces movement of NaPi2a out of brush border microvilli in living cells in real time. We show that a dynamic actin cytoskeleton is required for NaPi2a removal from the BBM in response to PTH. In addition, we demonstrate that a myosin motor that has previously been shown to be coregulated with NaPi2a, myosin VI, is necessary for PTH-induced removal of NaPi2a from BBM microvilli.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Hormone / Cell Membrane / Actins / Myosin Heavy Chains / Sodium-Phosphate Cotransporter Proteins, Type IIa / Kidney Tubules, Proximal Limits: Animals Language: En Journal: Am J Physiol Cell Physiol Journal subject: FISIOLOGIA Year: 2009 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Hormone / Cell Membrane / Actins / Myosin Heavy Chains / Sodium-Phosphate Cotransporter Proteins, Type IIa / Kidney Tubules, Proximal Limits: Animals Language: En Journal: Am J Physiol Cell Physiol Journal subject: FISIOLOGIA Year: 2009 Document type: Article Affiliation country: United States