epidermal-growth-factor and calcium-phosphate--monobasic--anhydrous

epidermal-growth-factor has been researched along with calcium-phosphate--monobasic--anhydrous* in 3 studies

Other Studies

3 other study(ies) available for epidermal-growth-factor and calcium-phosphate--monobasic--anhydrous

ArticleYear
Induction of early growth response gene Egr2 by basic calcium phosphate crystals through a calcium-dependent protein kinase C-independent p44/42 mitogen-activated protein kinase pathway.
    Cells, tissues, organs, 2003, Volume: 174, Issue:1-2

    Using the reverse transcriptase-polymerase chain reaction we examined the effect of basic calcium phosphate (BCP) crystals on the induction of the early growth response gene Egr2 transcription and the signal transduction pathway involved. The results showed that BCP crystals induced Egr2 transcription up to 8-fold, peaking at 24 h after treatment. The induction of Egr2 was confirmed by transient transfection assays using an Egr2 promoter/luciferase reporter construct and could be inhibited by the p44/42 mitogen-activated protein kinase (MAPK)-specific inhibitor U0126, or by calcium chelator TMB-8, but not by the SAPK2/p38 MAPK inhibitor SB202190 or by the protein kinase C inhibitor bisindolylmaleimide I (Bis-I). Using the Mercury Pathway Profiling System (Clontech, Palo Alto, Calif., USA) we further showed that induced Egr2 could stimulate the activities of several transcription factors that are associated with cell proliferation, such as c-fos, SRF and c-myc.

    Topics: Animals; Base Sequence; Calcium; Calcium Phosphates; Cells, Cultured; Crystallization; DNA-Binding Proteins; Early Growth Response Protein 2; Epidermal Growth Factor; Fibroblasts; Gene Expression Regulation; Humans; MAP Kinase Signaling System; Mitogen-Activated Protein Kinase 1; Mitogen-Activated Protein Kinase 3; Mitogen-Activated Protein Kinases; Molecular Sequence Data; Promoter Regions, Genetic; Protein Kinase C; Rabbits; RNA, Messenger; Synovial Membrane; Transcription Factors; Transcription, Genetic

2003
Increased efficiency of gene transfection in primary cultures of adult rat hepatocytes stimulated to proliferate: a comparative study using the lipofection and the calcium phosphate precipitate methods.
    Cell biology international reports, 1992, Volume: 16, Issue:7

    Transfection of the beta-galactosidase gene in quiescent cultures of adult rat hepatocytes with the calcium phosphate precipitate or the lipofection methods gave a higher level of beta-galactosidase gene expression with the lipofection than with the calcium phosphate precipitate method, but the transfection efficiency was weak in both cases. Transfection of hepatocytes stimulated to proliferate before transfection either in vivo by partial hepatectomy or in vitro by epidermal growth factor was more efficient than transfection of quiescent hepatocytes, and the lipofection method gave better results than the calcium phosphate precipitate method.

    Topics: Animals; beta-Galactosidase; Calcium Phosphates; Cell Division; Cells, Cultured; Chemical Precipitation; Epidermal Growth Factor; Evaluation Studies as Topic; Genetic Techniques; Liposomes; Liver; Rats; Transfection

1992
The mitogenic response to stimulation with basic calcium phosphate crystals is accompanied by induction and secretion of collagenase in human fibroblasts.
    Arthritis and rheumatism, 1991, Volume: 34, Issue:8

    Synovial fluid basic calcium phosphate (BCP) crystals are associated with severe destructive arthropathies that are characterized by synovial proliferation and digestion of articular collagenous structures. BCP crystals are potent mitogens, which may account for this proliferation. The role of collagenase in articular degradation is controversial because, despite the massive loss of collagen, no studies have confirmed collagenolytic activity in synovial fluid, as originally reported. We investigated collagenase messenger RNA induction and enzyme activity in human foreskin fibroblasts proliferating in response to stimulation with BCP crystals, and analyzed the associated secreted proteins. Northern blots revealed a dose-dependent accumulation of collagenase message, evident by 4 hours and continuing to at least 36 hours, in BCP-stimulated cultures. One- and 2-dimensional polyacrylamide gel electrophoresis of conditioned media from BCP crystal-stimulated cultures revealed the selective induction of 2 proteins with molecular weight and pI values consistent with those of collagenase. Increased enzyme activity was also found. Thus, the mitogenic response of fibroblasts to BCP crystals is accompanied by collagenase induction and secretion, supporting the hypothesis that they act as a mediator of joint destruction in BCP crystal-associated arthropathies.

    Topics: Calcium Phosphates; Cells, Cultured; Crystallization; Dose-Response Relationship, Drug; Electrophoresis, Gel, Two-Dimensional; Enzyme Induction; Epidermal Growth Factor; Fibroblasts; Humans; Infant, Newborn; Male; Microbial Collagenase; RNA, Messenger; Serum Albumin, Bovine; Time Factors

1991