DDB1 maintains intestinal homeostasis by preventing cell cycle arrest
Before the tissue collapse at day 4, the Ki67+ proliferating cells in the transient amplifying region of crypts were already decreased in the small intestine (Fig. 1D, S3A and S3B), while this change was delayed in the large intestine at day 6 (Fig. [...]the TUNEL assay revealed that cell death was...
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Published in | Cell regeneration Vol. 11; no. 1; pp. 18 - 4 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Nature Singapore
01.06.2022
Springer Nature B.V SpringerOpen |
Subjects | |
Online Access | Get full text |
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Summary: | Before the tissue collapse at day 4, the Ki67+ proliferating cells in the transient amplifying region of crypts were already decreased in the small intestine (Fig. 1D, S3A and S3B), while this change was delayed in the large intestine at day 6 (Fig. [...]the TUNEL assay revealed that cell death was increased in the KO small intestine (Fig. [...]the decreased cell proliferation and increased death would contribute to the disruption of homeostasis. In summary, using the genetic mouse models and organoids, we demonstrate that DDB1 plays a critical role in the fast homeostatic renewal of the intestinal epithelium, which is achieved by reducing CDK inhibitor expression, preventing cell cycle arrest in the G1 phase and thus ensuring normal cell proliferation. |
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Bibliography: | SourceType-Scholarly Journals-1 ObjectType-Correspondence-1 content type line 14 content type line 23 |
ISSN: | 2045-9769 2045-9769 |
DOI: | 10.1186/s13619-022-00119-6 |