<正>The prenent study was designed to test the hypothesis that the inhibitory effect of elevated glucose levels on mesangial cell growth might be mediated by transforming growth factor β (TGF β). Increased glucose levels inhibited mesangial cell proliferation in a concentration dependent manner. The addition of a rabbit antipncine TGF β1 neutralizing antibody significantly enchanced the cell proliferation in both normal (5.5mM) and high (50mM) glucose media (12% and 30% respectively), and almost completely blocked the growth inhibition induced by high glucose media. TGF β assay demonstrated mesangial cells produced more active than latent TGF β after growth in high glucose media. We conclude that TGF β functions as an autocrine cytokine in mesangial cells growth and the production of TGF β is modulated by high glucose concentration. The growth inhibition induced by high glucose levels may be largely mediated by endogenous TGF β.
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Department of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
Department of Biochemistry Molecular Biophysics, Virginia Commonwealth University, MCV Campus, Richmond, VADepartment of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
Chan W.
Lin K.C.
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Department of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498Department of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
Lin K.C.
Lin P.-S.
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Department of Radiation Oncology, Virginia Commonwealth University, MCV Campus, Richmond, VADepartment of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
Lin P.-S.
Trachtman H.
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Long Island Jewish Hospital, New Hyde Park, NYDepartment of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
Trachtman H.
Chan J.C.M.
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Department of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
Department of Biochemistry Molecular Biophysics, Virginia Commonwealth University, MCV Campus, Richmond, VADepartment of Pediatrics, Virginia Commonwealth University, Medical College of Virginia Campus, Richmond, VA 23298-0498
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Thomas Jefferson Univ, Sch Med, Dept Med, Div Nephrol, Philadelphia, PA 19107 USAThomas Jefferson Univ, Sch Med, Dept Med, Div Nephrol, Philadelphia, PA 19107 USA
Wang, LW
Zhu, YQ
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Thomas Jefferson Univ, Sch Med, Dept Med, Div Nephrol, Philadelphia, PA 19107 USAThomas Jefferson Univ, Sch Med, Dept Med, Div Nephrol, Philadelphia, PA 19107 USA
Zhu, YQ
Sharma, K
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Thomas Jefferson Univ, Sch Med, Dept Med, Div Nephrol, Philadelphia, PA 19107 USAThomas Jefferson Univ, Sch Med, Dept Med, Div Nephrol, Philadelphia, PA 19107 USA
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Univ Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, CanadaUniv Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, Canada
Gawaziuk, J. P.
Ma, X.
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Univ Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, CanadaUniv Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, Canada
Ma, X.
Sheikh, F.
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Univ Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, CanadaUniv Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, Canada
Sheikh, F.
Cheng, Z-Q.
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Univ Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, CanadaUniv Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, Canada
Cheng, Z-Q.
Cattini, P. A.
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Univ Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, CanadaUniv Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, Canada
Cattini, P. A.
Stephens, N. L.
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Univ Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, CanadaUniv Manitoba, John Buhler Res Ctr, Fac Med, Dept Physiol, Winnipeg, MB R3E 3P4, Canada