Ischemia disrupts myosin Iβ in renal tubules

被引:6
作者
Boyd-White, J
Srirangam, A
Goheen, MP
Wagner, MC
机构
[1] Indiana Univ, Sch Med, Dept Med, Div Nephrol,Renal Epithelial Biol Expt Labs, Indianapolis, IN 46202 USA
[2] Indiana Univ, Richard L Roudebush Vet Affairs Med Ctr, Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 281卷 / 04期
关键词
kidney; cytoskeleton; motor; disease; actin;
D O I
10.1152/ajpcell.2001.281.4.C1326
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In these studies we have examined rat kidneys biochemically and microscopically to determine where myosin I beta is located before, during, and after an acute ischemic injury. Myosin I beta 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 I beta 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 I beta staining and an increase in its cytoplasmic staining. Interestingly, the return of the F-actin in the BB precedes the return of the myosin I beta, 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.
引用
收藏
页码:C1326 / C1335
页数:10
相关论文
共 40 条
[1]   A ROLE FOR MARCKS, THE ALPHA-ISOZYME OF PROTEIN-KINASE-C AND MYOSIN-I IN ZYMOSAN PHAGOCYTOSIS BY MACROPHAGES [J].
ALLEN, LAH ;
ADEREM, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (03) :829-840
[2]   PURIFICATION AND CHARACTERIZATION OF A MAMMALIAN MYOSIN-I [J].
BARYLKO, B ;
WAGNER, MC ;
REIZES, O ;
ALBANESI, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (02) :490-494
[3]   Regulation of the enzymatic and motor activities of myosin I [J].
Barylko, B ;
Binns, DD ;
Albanesi, JP .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2000, 1496 (01) :23-35
[4]   MECHANISMS OF ISCHEMIC ACUTE-RENAL-FAILURE [J].
BONVENTRE, JV .
KIDNEY INTERNATIONAL, 1993, 43 (05) :1160-1178
[5]   LECTIN-GOLD CYTO-CHEMISTRY REVEALS INTERCALATED CELL HETEROGENEITY ALONG RAT-KIDNEY COLLECTING DUCTS [J].
BROWN, D ;
ROTH, J ;
ORCI, L .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (03) :C348-C356
[6]   Protein trafficking and polarity in kidney epithelium: From cell biology to physiology [J].
Brown, D ;
Stow, JL .
PHYSIOLOGICAL REVIEWS, 1996, 76 (01) :245-297
[7]   Antigen retrieval in cryostat tissue sections and cultured cells by treatment with sodium dodecyl sulfate (SDS) [J].
Brown, D ;
Lydon, J ;
McLaughin, M ;
StuartTilley, A ;
Tyszkowski, R ;
Alper, S .
HISTOCHEMISTRY AND CELL BIOLOGY, 1996, 105 (04) :261-267
[8]  
CANTIELLO HF, 1991, AM J PHYSIOL, V261, P882
[9]  
CHACKO S, 1994, J BIOL CHEM, V269, P15803
[10]   CYTOSKELETAL DISSOCIATION OF EZRIN DURING RENAL ANOXIA - ROLE IN MICROVILLAR INJURY [J].
CHEN, J ;
DOCTOR, RB ;
MANDEL, LJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (03) :C784-C795