Literature DB >> 2071544

Platelet-derived growth factor activates phospholipase D and chemotactic responses in vascular smooth muscle cells.

C J Welsh1, K Schmeichel, K McBride.   

Abstract

Platelet-derived growth factor (BB dimer; PDGF-BB) stimulates a mitogenic response in A-10 vascular smooth muscle cells. In addition, PDGF-BB stimulates phospholipase D activity against phosphatidylcholine in A-10 cells. This response was observed as a rapid metabolism of phosphatidylcholine to phosphatidate and choline; a subsequent metabolism generates sustained levels of diacylglycerol. The accumulation of phosphatidylethanol, a transphosphatidylation product of phospholipase D, was obvious in PDGF-treated cells. PDGF-BB also stimulates a chemotactic response in A-10 cells. The concentrations of PDGF-BB required to stimulate mitogenesis, phospholipase D activity and chemotaxis are similar. This finding shows that PDGF induces a variety of cellular responses and suggests that these responses may share common metabolic pathways. That conception was tested by investigating the activity of the different PDGF dimers. PDGF-AA had little or no activity in A-10 cells for any of the responses measured. PDGF-AB and PDGF-BB were equally potent in stimulating mitogenic responses. However, the AB heterodimer was only half as active as PDGF-BB with respect to activation of phospholipase D and chemotactic responses. These results demonstrate that PDGF stimulates phospholipase D in vascular smooth muscle cells. In addition, the data indicate that different PDGF dimers can transduce varying signals and suggest a link between the mechanisms by which PDGF-BB activates phospholipase D and the chemotactic response.

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Year:  1991        PMID: 2071544     DOI: 10.1007/BF02630963

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  61 in total

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Authors:  E G BLIGH; W J DYER
Journal:  Can J Biochem Physiol       Date:  1959-08

Review 2.  Signaling through phosphatidylcholine breakdown.

Authors:  J H Exton
Journal:  J Biol Chem       Date:  1990-01-05       Impact factor: 5.157

Review 3.  Signal transduction by the platelet-derived growth factor receptor.

Authors:  L T Williams
Journal:  Science       Date:  1989-03-24       Impact factor: 47.728

4.  Phospholipase C-mediated hydrolysis of phosphatidylcholine is an important step in PDGF-stimulated DNA synthesis.

Authors:  P Larrodera; M E Cornet; M T Diaz-Meco; M Lopez-Barahona; I Diaz-Laviada; P H Guddal; T Johansen; J Moscat
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

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Authors:  S B Bocckino; P F Blackmore; P B Wilson; J H Exton
Journal:  J Biol Chem       Date:  1987-11-05       Impact factor: 5.157

6.  Second messenger function of phosphatidic acid in platelet activation.

Authors:  M H Kroll; G B Zavoico; A I Schafer
Journal:  J Cell Physiol       Date:  1989-06       Impact factor: 6.384

7.  Phospholipase D activation by the mitogens platelet-derived growth factor and 12-O-tetradecanoylphorbol 13-acetate in NIH-3T3 cells.

Authors:  P Ben-Av; M Liscovitch
Journal:  FEBS Lett       Date:  1989-12-18       Impact factor: 4.124

8.  Effect of phospholipase C-gamma overexpression on PDGF-induced second messengers and mitogenesis.

Authors:  B Margolis; A Zilberstein; C Franks; S Felder; S Kremer; A Ullrich; S G Rhee; K Skorecki; J Schlessinger
Journal:  Science       Date:  1990-05-04       Impact factor: 47.728

9.  Regulation of phospholipase D in HL-60 granulocytes. Activation by phorbol esters, diglyceride, and calcium ionophore via protein kinase- independent mechanisms.

Authors:  M M Billah; J K Pai; T J Mullmann; R W Egan; M I Siegel
Journal:  J Biol Chem       Date:  1989-05-25       Impact factor: 5.157

10.  Isoform-specific induction of actin reorganization by platelet-derived growth factor suggests that the functionally active receptor is a dimer.

Authors:  A Hammacher; K Mellström; C H Heldin; B Westermark
Journal:  EMBO J       Date:  1989-09       Impact factor: 11.598

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  2 in total

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2.  Fibroblast chemotaxis and prolidase activity modulation by insulin-like growth factor II and mannose 6-phosphate.

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  2 in total

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