Role of pyruvate carboxylase in fatty acid synthesis: Alterations during preadipocyte differentiation |
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Authors: | Julia C. Mackall M. Daniel Lane |
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Affiliation: | Department of Physiological Chemistry Johns Hopkins University School of Medicine Baltimore, Maryland 21205 USA |
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Abstract: | Transport of mitochondrial acetyl units to the cytoplasm for fatty acid synthesis via the citrate cleavage pathway requires replenishment of mitochondrial oxaloacetate. Pyruvate carboxylase is though to fulfill this role although compelling evidence has been lacking. During lipogenic differentiation of 3T3-L1 preadipocytes, pyruvate carboxylase activity rises 18-fold in close coordination with fat accumulation and the activity of ATP-citrate lyase, an established lipogenic enzyme. The activities of enzymes less directly related to lipogenesis rise only 3–5-fold while other unrelated enzymes do not increase significantly. These results indicate that pyruvate carboxylase is in fact a lipogenic enzyme. |
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