Isolated ileal interposition in enteroendocrine L cells differentiation
Isolated ileal interposition in enteroendocrine L cells differentiation
Isolated ileal interposition in enteroendocrine L cells differentiation
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function. It is clear that genes regulat<strong>in</strong>g cell cycle, proliferation, <strong>differentiation</strong>, and apoptosis<br />
are important components of the adaptation process (Drozdowski et al., 2009). 97 Several<br />
studies <strong>in</strong> humans and laboratory animals showed that after massive resection of the proximal<br />
small <strong>in</strong>test<strong>in</strong>e, the rema<strong>in</strong><strong>in</strong>g ileum exhibits morphological and functional adaptation <strong>in</strong> an<br />
attempt to preserve nutritional health by <strong>in</strong>creas<strong>in</strong>g <strong>ileal</strong> absorption of dietary nutrients. The<br />
authors of these studies concluded that the <strong>ileal</strong> adaptation mechanisms for peptide<br />
absorption are mediated by cell proliferation, i.e., villus hyperplasia and <strong>in</strong>test<strong>in</strong>al dilatation,<br />
which serves to <strong>in</strong>crease the absorption surface. 115<br />
Gastro<strong>in</strong>test<strong>in</strong>al epithelial <strong>cells</strong> are under constant regenerative pressure. To ma<strong>in</strong>ta<strong>in</strong><br />
Nature Preced<strong>in</strong>gs : doi:10.1038/npre.2011.6614.2 : Posted 30 Nov 2011<br />
homeostasis, there must be a balance among cell apoptosis, senescence, proliferation, and<br />
<strong>differentiation</strong>. The ma<strong>in</strong>tenance of this balance is attributed to gastro<strong>in</strong>test<strong>in</strong>al stem <strong>cells</strong>.<br />
These <strong>cells</strong> are able to replicate and give rise to <strong>cells</strong> identical to themselves and to <strong>cells</strong> that<br />
will differentiate <strong>in</strong>to each of the different cell types present <strong>in</strong> this tissue. 116 Small numbers of<br />
<strong>in</strong>test<strong>in</strong>al stem <strong>cells</strong> (between one and three) are found at the bottom of each of the<br />
Lieberkühn crypts, which are the <strong>in</strong>vag<strong>in</strong>ations that make up the <strong>in</strong>test<strong>in</strong>e’s proliferative<br />
component. These <strong>cells</strong> give rise to a transient population of progenitor <strong>cells</strong>, which divide<br />
quickly while migrat<strong>in</strong>g along villi towards the bowel lumen. Dur<strong>in</strong>g migration, these <strong>cells</strong><br />
commit to one of three different cell l<strong>in</strong>eages: secretory (goblet <strong>cells</strong>), absorptive<br />
(enterocytes), or enteroendocr<strong>in</strong>e. This is a cont<strong>in</strong>ual process <strong>in</strong> which the most differentiated<br />
<strong>cells</strong> are replaced at the top of the villi every four or five days. Another type of secretory cell,<br />
called Paneth <strong>cells</strong>, differentiates at the bottom of the crypts (Figure 2). 117