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相关概念视频

Glucose Homeostasis: Pancreatic Islets and Insulin Secretion01:27

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The pancreatic islets comprising only 1%-2% of the volume are highly vascularized and innervated mini-organs. They contain five endocrine cell types, including β cells that secrete insulin, which is synthesized as a single polypeptide chain, preproinsulin, processed to proinsulin, and finally to insulin and C-peptide. This process is complex and regulated, involving the Golgi complex, the endoplasmic reticulum, and the secretory granules of the β cell.
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Cells and Secretions of the Pancreas01:16

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The pancreas, a vital organ within the abdominal cavity, plays dual roles in the digestive and endocrine systems, collaborating with exocrine and endocrine cells to maintain optimal digestion and blood sugar levels.
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The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
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The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
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Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
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The endocrine system is an extensive network of glands – organs or tissues in the body that create chemicals that control many bodily functions, that secrete hormones, which are chemical messengers that play essential roles in regulating various bodily functions. These hormones are secreted into the bloodstream and travel throughout the body. They require specific receptors to convey signals to cells possessing these corresponding receptors. This complex signaling mechanism ensures that...
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异质的内分泌细胞组成定义了人类小岛的功能表型.

Carmella Evans-Molina1,2,3,4,5,6,7, Yasminye D Pettway8, Diane C Saunders9

  • 1Departments of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

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概括

人的小岛细胞组成有很大的变化,影响激素分泌和2型糖尿病风险. 德尔塔细胞的丰富性显示出与胰岛素分泌和糖尿病遗传风险的最强联系.

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人类小岛屿的人类小岛屿在T1D中,它是T1D.T2D遗传风险得分得分T2D遗传风险得分阿尔法细胞是阿尔法细胞.贝塔细胞 贝塔细胞 贝塔细胞德尔塔细胞是三角洲细胞.葡萄糖激素分泌的分泌物胰岛素分泌的胰岛素分泌.

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科学领域:

  • 内分泌学 在内分泌学.
  • 遗传学 是一个遗传学.
  • 代谢疾病 代谢疾病

背景情况:

  • 综合小岛分发计划 (IIDP) 提供标准化的人类小岛准备研究.
  • 了解人类小岛的异质性对于糖尿病研究和治疗开发至关重要.

研究的目的:

  • 分析非糖尿病供体中人类小岛细胞组成的异质性.
  • 调查岛屿细胞组成,激素分泌和与2型糖尿病 (T2D) 相关的遗传因素之间的关联.

主要方法:

  • 来自299名没有糖尿病的器官捐赠者的人类小岛的表型和基因型.
  • 分析管道整合多种数据类型,以评估小岛细胞组成和分泌特征.

主要成果:

  • 在小岛细胞组成 (α,β,delta细胞) 中观察到实质性的异质性.
  • 岛屿细胞组成与荷尔蒙分泌特征,性别,种族/民族,祖先和T2D遗传风险有关.
  • 德尔塔细胞的丰富性显示出与胰岛素分泌和T2D遗传风险评分 (GRS) 最强的关联.

结论:

  • 人类小岛的异质性与各种因素有关,包括遗传学和供体特征.
  • 德尔塔细胞的丰富性是胰岛素分泌和T2D风险的关键因素,表明潜在的治疗点.
  • 这些发现为个性化医疗和糖尿病β细胞替代疗法的策略提供了信息.