A1 Refereed original research article in a scientific journal

Vimentin Suppresses Inflammation and Tumorigenesis in the Mouse Intestine




AuthorsWang Linglu, Mohanasundaram Ponnuswamy, Lindström Michelle, Asghar Muhammad Naheem, Sultana Giulia, Misiorek Julia O., Jiu Yaming, Chen Hongbo, Chen Zhi, Toivola Diana M., Cheng Fang, Eriksson John E.

PublisherFRONTIERS MEDIA SA

Publication year2022

JournalFrontiers in cell and developmental biology

Journal name in sourceFRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY

Journal acronymFRONT CELL DEV BIOL

Article number 862237

Volume10

Number of pages13

ISSN2296-634X

eISSN2296-634X

DOIhttps://doi.org/10.3389/fcell.2022.862237

Web address https://doi.org/10.3389/fcell.2022.862237

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/175279725


Abstract
Vimentin has been implicated in wound healing, inflammation, and cancer, but its functional contribution to intestinal diseases is poorly understood. To study how vimentin is involved during tissue injury and repair of simple epithelium, we induced colonic epithelial cell damage in the vimentin null (Vim(-/-)) mouse model. Vim(-/-) mice challenged with dextran sodium sulfate (DSS) had worse colitis manifestations than wild-type (WT) mice. Vim(-/-) colons also produced more reactive oxygen and nitrogen species, possibly contributing to the pathogenesis of gut inflammation and tumorigenesis than in WT mice. We subsequently describe that CD11b(+) macrophages served as the mainly cellular source of reactive oxygen species (ROS) production via vimentin-ROS-pSTAT3-interleukin-6 inflammatory pathways. Further, we demonstrated that Vim(-/-) mice did not develop colitis-associated cancer model upon DSS treatment spontaneously but increased tumor numbers and size in the distal colon in the azoxymethane/DSS model comparing with WT mice. Thus, vimentin has a crucial role in protection from colitis induction and tumorigenesis of the colon.

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