PTH-induced internalization of apical membrane NaPi2a: role of actin and myosin VI
Author(s) -
Judith Blaine,
Kayo Okamura,
Héctor Giral,
Sophia Y. Breusegem,
Yupanqui Caldas,
Andrew C. Millard,
Nicholas P. Barry,
Moshe Levi
Publication year - 2009
Publication title -
ajp cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.432
H-Index - 181
eISSN - 1522-1563
pISSN - 0363-6143
DOI - 10.1152/ajpcell.00260.2009
Subject(s) - brush border , internalization , parathyroid hormone , actin , cotransporter , myosin , microbiology and biotechnology , chemistry , cytoskeleton , actin cytoskeleton , apical membrane , biophysics , medicine , endocrinology , calcium , membrane , biochemistry , biology , sodium , vesicle , cell , organic chemistry
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.
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