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From the Department of Pathology, University of Washington, Seattle, and the Department of Biology (K.L.H.), San Diego State University, San Diego, Calif.
Correspondence to Dr Joan M. Lemire, University of Washington, Department of Pathology, Box 357470, Seattle, WA 98195-7470. E-mail joanlemi@u.washington.edu.
Abstract Smooth muscle cells (SMCs) with distinct
phenotypes are present in blood vessels, and distinct
culture types appear when SMCs are maintained in vitro. For example,
cultured SMCs from rat adult media grow as bipolar cells, which differ
in gene expression from the predominantly cobblestone-shaped SMCs
from rat pup aortas and rat neointimas that we call
SMCs. Since proteoglycans are present at different concentrations
in the normal intima and media and are elevated in atherosclerotic
plaque, we sought to determine whether
and adult medial SMC types
synthesize different or unique proteoglycans that are characteristic of
each phenotype. [35S]sulfate-labeled
proteoglycans were purified by ion-exchange
chromatography. An adult medial SMC line synthesized a
large proteoglycan (0.2 Kav on Sepharose CL-2B) that was
not detectable in a
SMC line. Digestion of this proteoglycan with
chondroitin ABC lyase revealed three core glycoproteins of
330, 370, and 450 kD. By Western blot analysis, the two
smallest of these reacted with two antibodies to the human fibroblast
proteoglycan versican. RNAs hybridizing to versican probes were found
only in adult medialtype SMCs, including an adult medial type
clone from pup aorta, by Northern blot analysis. Both SMC types
synthesize RNAs that hybridize to probes for other proteoglycans, such
as perlecan, biglycan, and decorin. We conclude that rat
SMC
cultures, unlike monkey, human, and rat adult medial SMC cultures,
express little or no versican. This difference in expression may be
responsible for the different morphologies and growth properties of the
two cell types.
Key Words: PG-M differentiation versican artery proteoglycans
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