We examined steady-state levels of mRNA encoding type IV collagen, B, chain of laminin, and the basement membrane heparan sulfate proteoglycan in the kidney cortex of a mouse model (KKAy) of non-insulindependent diabetes. mRNAs encoding laminin B, and the proteoglycan were unchanged in kidneys taken from diabetic mice with demonstrable basement membrane thickening. mRNA levels for type IV collagen, in contrast, were significantly elevated (2-fold) in diabetic mice concurrent with but not preceding morphologically thickened basement membranes. There was a negative correlation between a ratio of proteoglycan/type IV collagen and levels of albuminuria in the diabetic mice. No correlation was noted with laminin. We also examined the effects of inhibiting the synthesis of thromboxane, a potent vasoconstrictor, on the steady-state levels of type IV collagen in the diabetic mice. Inhibition of thromboxane stopped the progression of albuminuria and prevented an increase in type IV collagen mRNA levels. We conclude that basement membrane thickening in diabetes, a hallmark of diabetic nephropathy, is partly a consequence of an unbalanced increase in the production of type IV collagen. The relative decrease in proteoglycan production may contribute to chronic albuminuria.
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Original Articles|
February 01 1990
Altered Steady-State mRNA Levels of Basement Membrane Proteins in Diabetic Mouse Kidneys and Thromboxane Synthase Inhibition
Steven Ledbetter;
Steven Ledbetter
The Upjohn Company
Kalamazoo, Michigan
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, National Institutes of Health
Bethesda, Maryland
The Eye and Ear Institute, University of Pittsburgh
Pittsburgh, Pennsylvania
National Institute of Cancer Research
Genoa, Italy
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E Jill Copeland;
E Jill Copeland
The Upjohn Company
Kalamazoo, Michigan
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, National Institutes of Health
Bethesda, Maryland
The Eye and Ear Institute, University of Pittsburgh
Pittsburgh, Pennsylvania
National Institute of Cancer Research
Genoa, Italy
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Douglas Noonan;
Douglas Noonan
The Upjohn Company
Kalamazoo, Michigan
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, National Institutes of Health
Bethesda, Maryland
The Eye and Ear Institute, University of Pittsburgh
Pittsburgh, Pennsylvania
National Institute of Cancer Research
Genoa, Italy
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Gabriel Vogeli;
Gabriel Vogeli
The Upjohn Company
Kalamazoo, Michigan
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, National Institutes of Health
Bethesda, Maryland
The Eye and Ear Institute, University of Pittsburgh
Pittsburgh, Pennsylvania
National Institute of Cancer Research
Genoa, Italy
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John R Hassell
John R Hassell
The Upjohn Company
Kalamazoo, Michigan
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, National Institutes of Health
Bethesda, Maryland
The Eye and Ear Institute, University of Pittsburgh
Pittsburgh, Pennsylvania
National Institute of Cancer Research
Genoa, Italy
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Address correspondence and reprint requests to Steven Ledbetter, The Upjohn Company, Kalamazoo, Ml 49001.
Diabetes 1990;39(2):196–203
Article history
Received:
February 24 1989
Revision Received:
September 29 1989
Accepted:
September 29 1989
PubMed:
2227127
Citation
Steven Ledbetter, E Jill Copeland, Douglas Noonan, Gabriel Vogeli, John R Hassell; Altered Steady-State mRNA Levels of Basement Membrane Proteins in Diabetic Mouse Kidneys and Thromboxane Synthase Inhibition. Diabetes 1 February 1990; 39 (2): 196–203. https://doi.org/10.2337/diab.39.2.196
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