دورية أكاديمية

Genetic and Nongenetic Regulation of CAPN10 mRNA Expression in Skeletal Muscle.

التفاصيل البيبلوغرافية
العنوان: Genetic and Nongenetic Regulation of CAPN10 mRNA Expression in Skeletal Muscle.
المؤلفون: Nilsson, Emma A, Poulsen, Pernille, Storgaard, Heidi, Almgren, Peter, Ling, Charlotte, Jensen, Christine Bjørn, Madsbad, Sten, Groop, Leif, Vaag, Allan, Ridderstråle, Martin
المصدر: Diabetes; 54(10), pp 3015-3020 (2005) ; ISSN: 1939-327X
بيانات النشر: American Diabetes Association Inc.
سنة النشر: 2005
المجموعة: Lund University Publications (LUP)
مصطلحات موضوعية: Endocrinology and Diabetes
الوصف: The gene encoding calpain-10 (CAPN10) has been identified as a candidate gene for type 2 diabetes. Our aim was to study the impact of genetic (heritability and polymorphisms) and nongenetic (insulin, free fatty acids, and age) factors on CAPN10 mRNA expression in skeletal muscle using two different study designs. Muscle biopsies were obtained before and after hyperinsulinemic-euglycemic clamps from 166 young and elderly monozygotic and dizygotic twins as well as from 15 subjects with normal (NGT) or impaired glucose tolerance (IGT) exposed to an Intralipid infusion. We found hereditary effects on both basal and insulin-exposed CAPN10 mRNA expression. Carriers of the type 2 diabetes–associated single nucleotide polymorphism (SNP)-43 G/G genotype had reduced CAPN10 mRNA levels compared with subjects carrying the SNP-43 A-allele. Age had no significant influence on CAPN10 mRNA levels. Insulin had no significant effect on CAPN10 mRNA levels, neither in the twins nor in the basal state of the Intralipid study. However, after a 24-h infusion of Intralipid, we noted a significant increase in CAPN10 mRNA in response to insulin in subjects with NGT but not in subjects with IGT. In conclusion, we provide evidence that mRNA expression of CAPN10 in skeletal muscle is under genetic control. Glucose-tolerant but not glucose-intolerant individuals upregulate their CAPN10 mRNA levels in response to prolonged exposure to fat.
نوع الوثيقة: article in journal/newspaper
اللغة: English
ردمك: 978-0-00-232237-9
978-2-584-44776-1
0-00-232237-4
2-584-44776-2
العلاقة: https://lup.lub.lu.se/record/143376Test; http://dx.doi.org/10.2337/diabetes.54.10.3015Test; wos:000232237400026; pmid:16186407; scopus:25844477623
DOI: 10.2337/diabetes.54.10.3015
الإتاحة: https://doi.org/10.2337/diabetes.54.10.3015Test
https://lup.lub.lu.se/record/143376Test
رقم الانضمام: edsbas.C5140354
قاعدة البيانات: BASE
الوصف
ردمك:9780002322379
9782584447761
0002322374
2584447762
DOI:10.2337/diabetes.54.10.3015