Induction of CD44 and MMP expression by hyaluronidase treatment of articular chondrocytes

M Ohno-Nakahara, K Honda, K Tanimoto… - Journal of …, 2004 - academic.oup.com
M Ohno-Nakahara, K Honda, K Tanimoto, N Tanaka, T Doi, A Suzuki, K Yoneno, Y Nakatani…
Journal of biochemistry, 2004academic.oup.com
In this study, the effects of fragmentation of the glycosoaminoglycans of the cell-associated
matrix by hyaluronidase (HAase) on the expression of CD44 receptor and matrix
metalloproteinase (MMP) mRNAs in cultured articular chondrocytes were examined.
Chondrocytes, isolated from rabbit and bovine articular cartilage, were treated with bovine
testicular HAase (0–200 units/ml) in the presence or absence of an antibody for CD44. The
mRNA levels of CD44, CD44 variant (CD44v), MMPs (MMP-1,-3 and-9), and tissue inhibitors …
Abstract
In this study, the effects of fragmentation of the glycosoaminoglycans of the cell-associated matrix by hyaluronidase (HAase) on the expression of CD44 receptor and matrix metalloproteinase (MMP) mRNAs in cultured articular chondrocytes were examined. Chondrocytes, isolated from rabbit and bovine articular cartilage, were treated with bovine testicular HAase (0–200 units/ml) in the presence or absence of an antibody for CD44. The mRNA levels of CD44, CD44 variant (CD44v), MMPs (MMP-1, -3 and -9), and tissue inhibitors of metalloproteinases (TIMP-1 and TIMP-2) were determined by RT-PCR. The treatment of cultured chondrocytes with HAase resulted in the production of low molecular weight fragments of hyaluronan (HA). The expression of CD44, CD44v and MMP (MMP-1, -3 and -9) mRNAs, but not TIMP-1 or TIMP-2 mRNA, was up-regulated in the cultures treated with HAase, whereas this expression was not affected by treatment with purified HA of 1.0 × 105 Da. Furthermore, the induction of CD44 and MMPs on treatment with HAase was suppressed by an anti-CD44 antibody. The results suggest that the fragmentation of HA may lead to cartilage destruction in terms of the enhanced expression of MMPs as well as the upregulation of CD44.
Oxford University Press