World J Gastroenterol. 2010 Feb 7;16(5):538-46. doi: 10.3748/wjg.v16.i5.538.
The fact that the acid-secreting parietal cells undergo continuous renewal has been ignored by many gastroenterologists and cell biologists. In the past, it was thought that these cells were static. However, by using (3)H-thymidine radioautography in combination with electron microscopy, it was possible to demonstrate that parietal cells belong to a continuously renewing epithelial cell lineage. In the gastric glands, stem cells anchored in the isthmus region are responsible for the production of parietal cells. The stem cells give rise to three main progenitors: prepit, preneck and preparietal cells. Parietal cells develop either directly from the non-cycling preparietal cells or less commonly via differentiation of the cycling prepit and preneck cell progenitors. The formation of a parietal cell is a sequential process which involves diminishment of glycocalyx, production of cytoplasmic tubulovesicles, an increase in number and length of microvilli, an increase in number and size of mitochondria, and finally, expansion and invagination of the apical membrane with the formation of an intracellular canalicular system. Little is known about the genetic counterparts of these morphological events. However, the time dimension of parietal cell production and the consequences of its alteration on the biological features of the gastric gland are well documented. The production of a new parietal cell takes about 2 d. However, mature parietal cells have a long lifespan during which they migrate bi-directionally while their functional activity for acid secretion gradually diminishes. Following an average lifespan of about 54 d, in mice, old parietal cells undergo degeneration and elimination. Various approaches for genetic alteration of the development of parietal cells have provided evidence in support of their role as governors of the stem/progenitor cell proliferation and differentiation programs. Revealing the dynamic features and the various roles of parietal cells would help in a better understanding of the biological features of the gastric glands and would hopefully help in providing a basis for the development of new strategies for prevention, early detection and/or therapy of various gastric disorders in which parietal cells are involved, such as atrophic gastritis, peptic ulcer disease and gastric cancer.
壁细胞不断更新这一事实长期以来一直被许多胃肠病学家和细胞生物学家所忽视。过去,人们认为这些细胞是静态的。然而,通过使用(3)H-胸腺嘧啶放射自显影术结合电子显微镜,有可能证明壁细胞属于不断更新的上皮细胞谱系。在胃腺中,锚定在峡部区域的干细胞负责产生壁细胞。干细胞产生三种主要的祖细胞:前胃小凹、前颈和前壁细胞。壁细胞要么直接从非循环的前壁细胞发育而来,要么不太常见地通过循环的前胃小凹和前颈细胞祖细胞的分化而来。壁细胞的形成是一个连续的过程,涉及糖萼的减少、细胞质小管泡的产生、微绒毛数量和长度的增加、线粒体数量和大小的增加,最后,顶膜的扩展和内陷,形成细胞内管腔系统。关于这些形态事件的遗传对应物知之甚少。然而,壁细胞产生的时间维度及其对胃腺生物学特征的改变的后果已经有很好的记录。一个新的壁细胞的产生大约需要 2 天。然而,成熟的壁细胞有很长的寿命,在此期间,它们双向迁移,而它们的酸分泌功能逐渐减弱。在老鼠中,大约 54 天后,旧的壁细胞经历退化和消除。各种改变壁细胞发育的遗传方法为支持它们作为干细胞/祖细胞增殖和分化程序的调控者的作用提供了证据。揭示壁细胞的动态特征和各种作用将有助于更好地理解胃腺的生物学特征,并有望为预防、早期发现和/或治疗各种涉及壁细胞的胃部疾病提供新策略的基础,如萎缩性胃炎、消化性溃疡病和胃癌。