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Identification of a lymphocyte-produced cysteine proteinase based on its binding to. cap alpha. -macroglobulin (. cap alpha. M)

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5392992
Proteinases play a role in collagen vascular diseases. However, the role of lymphocytes in the production of these proteinases is poorly understood. Rabbit lymph node cells (LNC) were cultured with /sup 35/S-methionine or /sup 14/C-leucine. When culture supernatants were analyzed by radioimmunoelectrophoresis using an anti-rabbit ..cap alpha..M antiserum, radio-active ..cap alpha..M-precipitin arcs developed. LNC biosynthetically labeled in serum-free medium generated supernatants that, upon incubation with normal rabbit serum, yielded radio-active ..cap alpha..M precipitin arcs. Purified B and T cells as well as human T and B cell lines were labeled separately under identical conditions. Analysis revealed the presence of radiolabeled ..cap alpha..M molecules. T cells usually generated less intense radioactive ..cap alpha..M precipitin arcs than B cells. Thoracic duct lymphocytes also produced radioactive ..cap alpha..M precipitin arcs. They treated radiolabeled supernatants with a variety of proteinase inhibitors before reacting them with rabbit serum. Only inhibitors specific for cysteine or thiol proteinases were effective in abolishing radioactivity associated with ..cap alpha..M. It appears that lymphocytes actively produce a cysteine or thiol proteinase which, theoretically, is capable of degrading collagen.
Research Organization:
Univ. of Illinois, Chicago
OSTI ID:
5392992
Report Number(s):
CONF-8604222-
Conference Information:
Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 45:3
Country of Publication:
United States
Language:
English

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