Department of Neurobiology, Physiology & Behavior, College of Biological Sciences, University of California, Davis, CA, 95616, USA.
Department of Physiology and Membrane Biology, School of Medicine, University of California, Davis, CA, 95616, USA.
Bioessays. 2018 Nov;40(11):e1800119. doi: 10.1002/bies.201800119. Epub 2018 Sep 28.
We recently discovered a novel subset of beta cells that resemble immature beta cells during pancreas development. We named these "virgin" beta cells as they do not stem from existing mature beta cells. Virgin beta cells are found exclusively at the islet periphery in areas that we therefore designated as the "neogenic niche." As beta cells are our only source of insulin, their loss leads to diabetes. Islets also contain glucagon-producing alpha cells and somatostatin-producing delta cells, that are important for glucose homeostasis and form a mantle surrounding the beta cell core. This 3D architecture is important and determines access to blood flow and innervation. We propose that the distinctive islet architecture may also play an important, but hitherto unappreciated role in generation of new endocrine cells, including beta cells. We discuss several predictions to further test the contribution of the neogenic niche to beta cell regeneration.
我们最近发现了一类新型的β细胞亚群,它们在胰腺发育过程中类似于未成熟的β细胞。我们将这些细胞命名为“原始”β细胞,因为它们并非起源于现有的成熟β细胞。原始β细胞仅存在于胰岛的周边区域,我们将这些区域指定为“新生巢”。由于β细胞是我们体内胰岛素的唯一来源,其缺失会导致糖尿病。胰岛还包含产生胰高血糖素的α细胞和产生生长抑素的δ细胞,它们对于葡萄糖稳态非常重要,并形成围绕β细胞核心的外衣。这种 3D 结构非常重要,决定了其对血流和神经支配的可及性。我们提出,独特的胰岛结构可能在新的内分泌细胞(包括β细胞)的生成中也发挥着重要作用,但迄今尚未得到重视。我们讨论了几个预测,以进一步检验新生巢对β细胞再生的贡献。