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In This Issue of Diabetes

机译:在本期糖尿病

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According to Lam et al. (p. 674), a novel population of highly proliferative hormone-negative islet cells may exist in human pancreata, and there is a hint that they might play an essential role in islet function and growth. Using a large collection of nondiabetic and type 1 diabetes human pancreas samples, the authors initially focused on the protein Ki67 as a marker of cell proliferation and reportedly found populations of proliferative islet cells. However, the population showed no signs of expressing insulin or that they were lymphocytes or endothelial cells. The question then was what were they. The authors report that pancreatic polypeptide, somatostatin, and ghrelin cells showed no real sign of proliferation. In contrast, glucagon-expressing α-cells were proliferative but only comprised about one-third of the total population of proliferative islet cells. The majority of the population was reportedly negative for any hormone expression. The focus then moved to the possibility that the proliferative cells might express markers of islet endocrine progenitors. After excluding one key progenitor (Ngn3), they found that most of the hormone-negative proliferative cells uniformly contained immunoreactivity for Sox9 (typically present in islet progenitors) and ARX (an α-cell marker). There were also various markers of islet endocrine cells and of various potential cellular functions. Author Jake A. Kushner told Diabetes. "Given previous work that reveals an age-dependent decline in p-cell proliferation, we were genuinely shocked to find these high-proliferative islet endocrine cells in adult pancreata. But, what does the presence of these cells mean? Honestly, we don't know. The most obvious implication is that islets might retain some degree of plasticity into adulthood. These highly proliferative islet endocrine cells may play an unknown role in islet growth and/or regeneration. We're eager to see where this research leads and hopeful that our findings could someday translate to help patients with diabetes."
机译:据林等。 (p。674),人胰腺中可能存在一种新的高度增殖的激素阴性胰岛细胞群体,提示它们可能在胰岛功能和生长中起重要作用。利用大量的非糖尿病和1型糖尿病人胰腺样本,作者最初着眼于蛋白Ki67作为细胞增殖的标志物,据报道发现了增殖的胰岛细胞群。但是,该人群没有表达胰岛素的迹象,或者它们是淋巴细胞或内皮细胞。那么问题是他们是什么。作者报告说,胰腺多肽,生长抑素和生长素释放肽细胞没有显示出真正的增殖迹象。相反,表达胰高血糖素的α细胞是增殖性的,但是仅占增殖性胰岛细胞总数的约三分之一。据报道,大多数人口的任何激素表达均为阴性。然后焦点转移到增殖细胞可能表达胰岛内分泌祖细胞标记的可能性。在排除了一个关键祖细胞(Ngn3)之后,他们发现大多数荷尔蒙阴性增殖细胞均对Sox9(通常存在于胰岛祖细胞中)和ARX(α细胞标记物)均匀地具有免疫反应性。胰岛内分泌细胞也有各种标记物,并且具有各种潜在的细胞功能。作者Jake A. Kushner告诉《糖尿病》。 “鉴于先前的工作揭示了p细胞增殖的年龄依赖性下降,我们真为震惊地发现了成年胰腺中这些高增殖性胰岛内分泌细胞。但是,这些细胞的存在是什么意思呢?我们知道,最明显的暗示是胰岛到成年后可能会保留一定程度的可塑性,这些高度增殖的胰岛内分泌细胞可能在胰岛的生长和/或再生中起未知的作用,我们渴望看到这项研究的方向并充满希望我们的发现有一天可能会转化为对糖尿病患者的帮助。”

著录项

  • 来源
    《Diabetes》 |2018年第4期|535-536|共2页
  • 作者

    Max Bingham;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:46:01

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