Abstract |
MBA-2.1 cells produce an activity, designated restrictin-P, which is specifically inhibitory to the growth of plasmacytomas and mature B cell lymphomas. We examined whether the activity of this stromally derived glycoprotein could be attributed to a well-characterized growth factor. Restrictin-P-producing cells were therefore screened for the expression of transcripts of a variety of growth suppressors. With the exception of TGF-beta 1, none was produced in detectable amounts by these cells. Furthermore, recombinant forms of the inhibitory molecules tested did not exert a biological effect similar to that of restrictin-P. Restrictin-P was shown to elicit a G0/G1 arrest in the cell cycle of its target cells, as soon as 24 h after their exposure to the inhibitor. This effect could not be mimicked by TGF-beta 1. We suggest that restrictin-P is part of a novel family of inhibitors which are required for the maintenance of cell-type specificities in the hematopoietic microenvironment.
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Authors | J Honigwachs-Sha'anani, N Brosh, R Kompier, A Kadouri, D Zipori |
Journal | Annals of the New York Academy of Sciences
(Ann N Y Acad Sci)
Vol. 628
Pg. 287-97
( 1991)
ISSN: 0077-8923 [Print] United States |
PMID | 2069309
(Publication Type: Journal Article)
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Chemical References |
- Cytokines
- Glycoproteins
- Growth Inhibitors
- Intercellular Signaling Peptides and Proteins
- RNA, Messenger
- Transforming Growth Factor beta
- restrictin-P
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Topics |
- Animals
- Cell Cycle
(drug effects)
- Cell Line
- Cytokines
(genetics)
- Flow Cytometry
- Glycoproteins
(genetics, isolation & purification, pharmacology)
- Growth Inhibitors
(genetics, isolation & purification, pharmacology)
- Intercellular Signaling Peptides and Proteins
- Plasmacytoma
- RNA, Messenger
(genetics)
- Transforming Growth Factor beta
(pharmacology)
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