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Expression of CD44 in kidney after acute ischemic injury in rats
George M. O'Brien Kidney and Urological Diseases Center, Renal Division, Departments of Medicine and Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110 De novo CD44 and ligand expression at wound margins accompanies cellular proliferation and migrat...
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Published in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2000-01, Vol.278 (1), p.247-R254 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
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Summary: | George M. O'Brien Kidney and Urological Diseases Center, Renal
Division, Departments of Medicine and Cell Biology and Physiology,
Washington University School of Medicine, St. Louis, Missouri 63110
De novo CD44 and ligand expression at
wound margins accompanies cellular proliferation and migration that
effect repair of injured mucosal and vascular endothelial tissues. To
determine whether CD44 could play a role in recovery from acute
ischemic renal injury, we characterized its renal expression and those of two of its ligands, hyaluronic acid and osteopontin. Although no
expression is detectable in nonischemic kidneys, several mRNAs for CD44
are present within 1 day after injury. CD44 mRNA is expressed in
proximal tubules undergoing repair. CD44 peptide is present in basal
and lateral cell membranes. Hyaluronic acid is normally expressed in
the interstitium of the renal papilla only. By 1 day
postischemia, hyaluronic acid can be detected, in addition, in
the interstitium surrounding regenerating tubules. Osteopontin, not
normally expressed in the renal proximal tubule, is expressed in
regenerating tubules by 3 days after induction of acute ischemic injury. Immunoreactive osteopontin peptide continues to be localized in
those tubules still undergoing repair for as long as 7 days after the
injury. Our data are consistent with a role for CD44-ligand interactions in the regenerating proximal tubule participating in the
process of recovery after ischemic injury.
acute renal failure; hyaluronic acid; matrix; osteopontin; arginine-glycine-aspartate peptides |
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ISSN: | 0363-6119 1522-1490 |
DOI: | 10.1152/ajpregu.2000.278.1.R247 |