Abstract

The functional integrity of the intestinal epithelial barrier relies on tight coordination of cell proliferation and migration, with failure to regulate these processes resulting in disease. It is not known whether cell proliferation is sufficient to drive epithelial cell migration during homoeostatic turnover of the epithelium. Nor is it known precisely how villus cell migration is affected when proliferation is perturbed. Some reports suggest that proliferation and migration may not be related while other studies support a direct relationship. We used established cell-tracking methods based on thymine analog cell labeling and developed tailored mathematical models to quantify cell proliferation and migration under normal conditions and when proliferation is reduced and when it is temporarily halted. We found that epithelial cell migration velocities along the villi are coupled to cell proliferation rates within the crypts in all conditions. Furthermore, halting and resuming proliferation results in the synchronized response of cell migration on the villi. We conclude that cell proliferation within the crypt is the primary force that drives cell migration along the villus. This methodology can be applied to interrogate intestinal epithelial dynamics and characterize situations in which processes involved in cell turnover become uncoupled, including pharmacological treatments and disease models.—Parker, A., Maclaren, O. J., Fletcher, A. G., Muraro, D., Kreuzaler, P. A., Byrne, H. M., Maini, P. K., Watson, A. J. M., Pin, C. Cell proliferation within small intestinal crypts is the principal driving force for cell migration on villi.

Highlights

  • The epithelial lining of the intestine undergoes continual renewal; adult stem cells at the base of intestinal crypts proliferate and differentiate into multiple functionally distinct epithelial subtypes, which migrate upward to the villus tips to eventually be shed into the gut lumen [1, 2]

  • The functional integrity of the intestinal epithelial barrier relies on tight coordination of cell proliferation and migration, with failure to regulate these processes resulting in disease

  • We studied the relationship between crypt cell production and villus cell migration in the proximal and distal small intestine of C57BL/6 mice; in transgenic Omomyc mice, which exhibit reduced cell proliferation in the intestinal epithelium [29]; and in C57BL/6 mice treated with the cytostatic/cytotoxic agent cytosine arabinoside (Ara-C) at doses that temporarily halted cell proliferation

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Summary

Introduction

The epithelial lining of the intestine undergoes continual renewal; adult stem cells at the base of intestinal crypts proliferate and differentiate into multiple functionally distinct epithelial subtypes, which migrate upward to the villus tips to eventually be shed into the gut lumen [1, 2]. ABBREVIATIONS: Ara-C, cytosine arabinoside; BrdU, 5-bromo-29-deoxyuridine; CVEU, crypt–villus epithelial unit; DAB, 3,39-diaminobenzidine; H3, histone 3; HRP, horseradish peroxidase; IdU, 5-iodo-29-deoxyuridine; pH3, phospho-histone 3. Cell migration on the villus has been found to exhibit a circadian rhythm, which is not observed in cell proliferation in the crypt [19] Active migration processes, such as those seen during wound healing [20,21,22,23], have been proposed to explain apparent disparities between proliferation and migration The FASEB Journal Vol., No.2 ,0p8p9:623-66-663489,/1A7p/r0il0, 23011-70636 © The Author(s) rates, whereas an alternative explanation for uncoupling between crypt and villus cell migration is the contribution of whole villus contraction and expansion [24, 25]

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