Am J Physiol Cell Physiol  AJP: Regulatory, Integrative and Comparative Physiology
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Am J Physiol Cell Physiol 281: C1326-C1335, 2001;
0363-6143/01 $5.00
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Vol. 281, Issue 4, C1326-C1335, October 2001

Ischemia disrupts myosin Ibeta in renal tubules

Judy Boyd-White1, Anjaiah Srirangam1, Michael P. Goheen2, and Mark C. Wagner1

1 Renal Epithelial Biology Experimental Laboratories, Division of Nephrology, Department of Medicine, and 2 Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Roudebush Veterans Affairs Medical Center, Indianapolis, Indiana 46202

In these studies we have examined rat kidneys biochemically and microscopically to determine where myosin Ibeta is located before, during, and after an acute ischemic injury. Myosin Ibeta is present in multiple tubule segments including the brush border (BB) of the proximal tubule cell (PTC). Its distribution is severely altered by a 15-min renal artery clamp. Myosin Ibeta is present in the urine during reflow and is found in the numerous cellular blebs arising from the damaged PTC and other tubules. Two hours of reflow result in a decrease in BB myosin Ibeta staining and an increase in its cytoplasmic staining. Interestingly, the return of the F-actin in the BB precedes the return of the myosin Ibeta , suggesting that this myosin I isoform may not play a role in rebuilding the microvilli after an ischemic injury. A nonstructural role for this myosin, such as transport or channel regulation, is supported by its presence in many tubule segments, all of which have transport and channel requirements but do not all contain microvilli.

kidney; cytoskeleton; motor; disease; actin


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M. C. Wagner, B. L. Blazer-Yost, J. Boyd-White, A. Srirangam, J. Pennington, and S. Bennett
Expression of the unconventional myosin Myo1c alters sodium transport in M1 collecting duct cells
Am J Physiol Cell Physiol, July 1, 2005; 289(1): C120 - C129.
[Abstract] [Full Text] [PDF]




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