An important function of CD44 is to act as a cellular receptor for hyaluron
ic acid and osteopontin. Cell-matrix interactions mediated by the CD44/hyal
uronic acid receptor-ligand pair are involved in the regulation of leukocyt
e migration and activation. Osteopontin is a molecule associated with cell
adhesion and migration and functions through binding to CD44. This study ex
amined whether CD44, hyaluronic acid and osteopontin participate in the pro
gression of IgA nephropathy. CD44 was expressed in mesangial cells, crescen
ts, tubular cells and interstitial infiltrating cells in areas of tubuloint
erstitial injury. Hyaluronic acid was deposited in the capillary tuft of ad
hesion, crescents and the periglomerular area, and around damaged tubules.
Osteopontin was expressed in tubular cells and interstitial infiltrating ce
lls in areas of tubulointerstitial injury. The glomerular and interstitial
deposition of hyaluronic acid correlated with the glomerular and interstiti
al expression of CD44. The interstitial expression of CD44 correlated with
the interstitial expression of osteopontin. The expression of both CD44 and
osteopontin in the interstitium correlated with the extent of tubulointers
titial damage. The expression of CD44 in the interstitium correlated with t
he severity of chronic glomerular lesions. The glomerular and interstitial
CD44 and hyaluronic acid expression correlated with proteinuria, and inters
titial CD44 and hyaluronic acid expression correlated with creatinine clear
ance rate. In summary, this study suggests that CD44 participates in the pr
ogression of IgA nephropathy by binding hyaluronic acid and osteopontin. Co
pyright (C) 2001 S. Karger AG, Basel.