RELATIVE EXPRESSION OF INSULIN-RECEPTOR ISOFORMS DOES NOT DIFFER IN LEAN, OBESE, AND NONINSULIN-DEPENDENT DIABETES-MELLITUS SUBJECTS
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ANDERSON, CM
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UNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USAUNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USA
ANDERSON, CM
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HENRY, RR
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UNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USAUNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USA
HENRY, RR
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KNUDSON, PE
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UNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USAUNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USA
KNUDSON, PE
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OLEFSKY, JM
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UNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USAUNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USA
OLEFSKY, JM
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WEBSTER, NJG
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UNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USAUNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USA
WEBSTER, NJG
[1
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[1] UNIV CALIF SAN DIEGO, MED CTR, DEPT MED, DIV ENDOCRINOL, SAN DIEGO, CA 92161 USA
The insulin receptor is expressed as two isoforms that differ by a 12-amino acid region at the carboxy-terminus of the alpha-subunit encoded by exon 11. These isoforms are produced by tissue-specific alternate splicing of the insulin receptor mRNA. To determine whether the relative expression of the isoforms is altered in skeletal muscle in two insulin-resistant states, NIDDM and obesity, relative mRNA levels were measured using a polymerase chain reaction technique. There were no differences in the relative amounts of skeletal muscle mRNA encoding the exon 11-containing form compared to the exon 11-lacking form of the insulin receptor among lean normal (30 +/- 2% Ex11-), obese nondiabetic (32 +/- 2%), and NIDDM (31 +/- 1%) subjects. We conclude that altered expression of insulin receptor isoform mRNAs does not account for skeletal muscle insulin resistance in NIDDM and obesity.