Chondrocyte activation in response to factor(s) produced by a continuous line of lapine synovial fibroblasts

Shoji Watanabe, Helga I. Georgescu, Deanna Mendelow, Christopher H. Evans

Research output: Contribution to journalArticle

34 Scopus citations

Abstract

We have established a permanent line of lapine synovial fibroblasts called HIG-82. Upon appropriate stimulation, these cells mimicked primary cultures of lapine synovial cells in producing substances which activated primary cultures of lapine articular chondrocytes. Activated chondrocytes secreted prostaglandin E2 (PGE2) and latent neutral collagenase, gelatinase, and caseinase, but not acid hydrolases, into their culture media. PGE2 itself did not activate the chondrocytes. Heating the crude, synovial-conditioned media at 70 °C for 30 min reduced their activating activity by 49.3 ± 20.5% (n = 7). Production of PGE2 by chondrocytes was maximal during the first day of exposure to synovial conditioned media, whereas the production of neutral proteinases peaked during the second day. All the chondrocyte-stimulating activity was present in a fraction of Mr 10 000-25 000. Unlike the crude conditioned medium, this partially-purified material retained full activity following heating to 70 °C for 30 min. These data indicate that synovial fibroblasts (type B synoviocytes) are a source of chondrocyte activator(s) and that neutral, but not acid, proteinases may be involved in extracellular proteolysis which leads to the resorption of the cartilaginous matrix seen in bioassays of catabolin.

Original languageEnglish (US)
Pages (from-to)218-226
Number of pages9
JournalExperimental Cell Research
Volume167
Issue number1
DOIs
StatePublished - Nov 1986

ASJC Scopus subject areas

  • Cell Biology

Fingerprint Dive into the research topics of 'Chondrocyte activation in response to factor(s) produced by a continuous line of lapine synovial fibroblasts'. Together they form a unique fingerprint.

  • Cite this