دورية أكاديمية

Lupenone attenuates thapsigargin-induced endoplasmic reticulum stress and apoptosis in pancreatic beta cells possibly through inhibition of protein tyrosine kinase 2 activity

التفاصيل البيبلوغرافية
العنوان: Lupenone attenuates thapsigargin-induced endoplasmic reticulum stress and apoptosis in pancreatic beta cells possibly through inhibition of protein tyrosine kinase 2 activity
المؤلفون: Seung-Eun Song, Su-Kyung Shin, Yong-Woon Kim, Young Rok Do, Ae Kyoung Lim, Jae-Hoon Bae, Gil-Saeng Jeong, Seung-Soon Im, Dae-Kyu Song
المساهمون: Do, Young Rok, Bae, Jae Hoon, Im, Seung Soon, Song, Dae Kyu, Dept. of Internal Medicine (내과학), Dept. of Physiology (생리학), 도영록, 배재훈, 임승순, 송대규
بيانات النشر: School of Medicine (의과대학)
سنة النشر: 2023
المجموعة: Keimyung University Medical Library: KUMeL Repository
مصطلحات موضوعية: 2-Aminoethoxydiphenyl borate (PubChem CID: 1598), 4-Phenylbutyric acid (PubChem CID: 4775), Apoptosis, Beta-cell, Cyclopiazonic acid (PubChem CID: 54695722), ER stress, KN-93 (PubChem CID: 5312122), Lupenone, Lupenone (PubChem CID: 92158), Protein tyrosine kinase 2, SP600125 (PubChem CID: 8515), Sodium orthovanadate (PubChem CID: 61671), Store-operated calcium entry, Streptozotocin (PubChem CID: 29327), Thapsigargin (PubChem CID: 446378), W-7 (PubChem CID: 124887)
الوصف: Aims: Prolonged high levels of cytokines, glucose, or free fatty acids are associated with diabetes, elevation of cytosolic Ca2+ concentration ([Ca2+]C), and depletion of Ca2+ concentration in the endoplasmic reticulum (ER) of pancreatic beta cells. This Ca2+ imbalance induces ER stress and apoptosis. Lupenone, a lupan-type triterpenoid, is beneficial in diabetes; however, its mechanism of action is yet to be clarified. This study evaluated the protective mechanism of lupenone against thapsigargin-induced ER stress and apoptosis in pancreatic beta cells. Materials and methods: MIN6, INS-1, and native mouse islet cells were used. Western blot for protein expressions, measurement of [Ca2+]C, and in vivo glucose tolerance test were mainly performed. Key findings: Thapsigargin increased the protein levels of cleaved caspase 3, cleaved PARP, and the phosphorylated form of JNK, ATF4, and CHOP. Thapsigargin increased the interaction between stromal interaction molecule1 (Stim1) and Orai1, enhancing store-operated calcium entry (SOCE). SOCE is further activated by protein tyrosine kinase 2 (Pyk2), which is Ca2+-dependent and phosphorylates the tyrosine residue at Y361 in Stim1. Lupenone inhibited thapsigargin-mediated Pyk2 activation, suppressed [Ca2+]C, ER stress, and apoptosis. Lupenone restored impaired glucose-stimulated insulin secretion effectuated by thapsigargin and glucose intolerance in a low-dose streptozotocin-induced diabetic mouse model. Significance: These results suggested that lupenone attenuated thapsigargin-induced ER stress and apoptosis by inhibiting SOCE; this may be due to the hindrance of Pyk2-mediated Stim1 tyrosine phosphorylation. In beta cells that are inevitably exposed to frequent [Ca2+]C elevation, the attenuation of abnormally high SOCE would be beneficial for their survival.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 1879-0631
العلاقة: https://kumel.medlib.dsmc.or.kr/handle/2015.oak/45276Test; https://www.sciencedirect.com/science/article/pii/S0024320523007427Test
DOI: 10.1016/j.lfs.2023.122107
الإتاحة: https://doi.org/10.1016/j.lfs.2023.122107Test
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/45276Test
https://www.sciencedirect.com/science/article/pii/S0024320523007427Test
رقم الانضمام: edsbas.D4F12B05
قاعدة البيانات: BASE
الوصف
تدمد:18790631
DOI:10.1016/j.lfs.2023.122107