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PMID: 6691142 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Heterogeneity of normal human diploid fibroblasts: isolation and characterization of one phenotype.

Science (New York, N.Y.) ·Vol. 223 ·No. 4632 ·1984-01-13 ·Pages 171-3

Bordin S, Page RC, Narayanan AS

Abstract

Cultures of human diploid fibroblasts contain cells that respond to exposure to the first component of complement (C1) by initiating DNA synthesis and growth. The plasma membranes of these cells have specific binding sites for the C1q subcomponent of C1. A fluorescence-activated cell sorter was used to isolate a subset of cells with a high affinity for C1q, and the growth and synthesis activities of these high-affinity cells were studied after numerous replications in vitro. These cells synthesize DNA and grow faster than the parent cultures and low-affinity cells, and they produce two to three times as much protein. About 40 percent of their total protein synthesis activity is directed to collagen production, unusually high proportions of collagen types III and V being produced. These properties and the high affinity of the cells for C1q are retained for at least six cell transfers. This phenotype has the properties expected of fibroblasts in healing wounds and inflamed tissues.

MeSH Terms
Carrier Proteins Cell Division Cell Separation Cells, Cultured Collagen/biosynthesis,classification DNA/biosynthesis Fibroblasts/analysis,cytology,physiology Flow Cytometry Gingiva Humans Hyaluronan Receptors Membrane Glycoproteins Mitochondrial Proteins Phenotype Protein Biosynthesis Receptors, Complement/analysis
Chemicals
C1QBP protein, human Carrier Proteins Hyaluronan Receptors Membrane Glycoproteins Mitochondrial Proteins Receptors, Complement complement 1q receptor Collagen DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bordin S
Page R C
Narayanan A S
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1984-01-13
Pages
171-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDCR NIH HHS · DE-02600 · United States
NIDCR NIH HHS · DE-03301 · United States
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