دورية أكاديمية
Role of autophagy in beta-cell function and mass
| العنوان: | Role of autophagy in beta-cell function and mass |
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| المؤلفون: | Hur, K. Y., Jung, H. S., Lee, M. -S. |
| بيانات النشر: | WILEY-BLACKWELL |
| سنة النشر: | 2010 |
| المجموعة: | Seoul National University: S-Space |
| مصطلحات موضوعية: | autophagy, ER stress, cell death |
| الوصف: | Type 2 diabetes (T2D) is characterized by decreased insulin secretion and action. Decreased insulin secretion results from a reduction in pancreatic beta-cell mass and/or function. Apoptosis, oxidative stress, mitochondrial dysfunction and endoplasmic reticulum (ER) stress responses including JNK activation have been suggested as mechanisms for the changes of pancreatic beta-cells in T2D; however, the underlying causes were not clearly elucidated. Autophagy is an intracellular process that plays crucial roles in cellular homeostasis through degradation and recycling of organelles. We have reported increased apoptosis and decreased proliferation of beta-cells with resultant reduction in the beta-cell mass in beta-cell-specific autophagy-deficient mice. Morphological analysis of beta-cells revealed accumulation of ubiquitinated proteins, swollen mitochondria and distended ER. Insulin secretory function ex vivo was also impaired. As a result, beta-cell-specific autophagy-deficient mice showed hypoinsulinaemia and hyperglycaemia. These results suggested that autophagy is necessary to maintain the structure, mass and function of pancreatic beta-cells. In addition, as autophagy may play a protective role against ER stress and rejuvenates organelle function, impaired autophagy may lead to mitochondrial dysfunction and ER stress, which have been implicated as potential causes of insulin resistance. Therefore, in addition to beta-cell homeostasis, dysregulated autophagy may possibly be involved in diverse aspects of the pathogenesis of diabetes. ; This work was supported by the 21C Frontier Functional Proteomics Project of the Korean Ministry of Science & Technology (FPR08B1-210) and Global Research Laboratory Grant (2010–00347). ; Komatsu M, 2010, NAT CELL BIOL, V12, P213, DOI 10.1038/ncb2021 ; Qin L, 2010, AUTOPHAGY, V6, P239 ; Novak I, 2010, EMBO REP, V11, P45, DOI 10.1038/embor.2009.256 ; Masiero E, 2009, CELL METAB, V10, P507, DOI 10.1016/j.cmet.2009.10.008 ; Zhang Y, 2009, P NATL ACAD SCI USA, V106, P19860, DOI ... |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 1462-8902 |
| العلاقة: | DIABETES OBESITY & METABOLISM; Vol.12; 20-26; http://hdl.handle.net/10371/77589Test |
| DOI: | 10.1111/j.1463-1326.2010.01278.x |
| الإتاحة: | https://doi.org/10.1111/j.1463-1326.2010.01278.xTest http://hdl.handle.net/10371/77589Test |
| رقم الانضمام: | edsbas.4AFCF5AE |
| قاعدة البيانات: | BASE |
| تدمد: | 14628902 |
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| DOI: | 10.1111/j.1463-1326.2010.01278.x |