Reduced susceptibility of mice overexpressing transforming growth factor α to dextran sodium sulphate induced colitis
Gut, 1998•gut.bmj.com
Background—Transforming growth factor α (TGF-α) knockout mice have increased
susceptibility to dextran sodium sulphate (DSS) induced colitis. Aim—To substantiate the
findings that TGF-α is a key mediator of colonic mucosal protection and/or repair
mechanisms by evaluating the susceptibility of mice overexpressing TGF-α to DSS induced
colitis. Methods—TGF-α overexpression was induced in transgenic mice by
ZnSO4administration in drinking water (TG+). Three groups were used as controls: one …
susceptibility to dextran sodium sulphate (DSS) induced colitis. Aim—To substantiate the
findings that TGF-α is a key mediator of colonic mucosal protection and/or repair
mechanisms by evaluating the susceptibility of mice overexpressing TGF-α to DSS induced
colitis. Methods—TGF-α overexpression was induced in transgenic mice by
ZnSO4administration in drinking water (TG+). Three groups were used as controls: one …
Background—Transforming growth factor α (TGF-α) knockout mice have increased susceptibility to dextran sodium sulphate (DSS) induced colitis.
Aim—To substantiate the findings that TGF-α is a key mediator of colonic mucosal protection and/or repair mechanisms by evaluating the susceptibility of mice overexpressing TGF-α to DSS induced colitis.
Methods—TGF-α overexpression was induced in transgenic mice by ZnSO4administration in drinking water (TG+). Three groups were used as controls: one transgenic group without ZnSO4 administration (TG−), and two non-transgenic littermate groups receiving ZnSO4 (Non-TG+) or only water (Non-TG−). Acute colitis was induced in all groups by administration of DSS (5%, w/v) in drinking water for six days ad libitum.
Results—About 35–39% of the entire colonic mucosa was destroyed in Non-TG−, Non-TG+, and TG− animals compared with 9% in TG+ mice. The crypt damage score was 18.7 (0.9), 18.2 (1.0), 18.9 (0.8), and 6.8 (1.5) (means (SEM)) in Non-TG−, Non-TG+, TG−, and TG+ mice respectively. Mucin and bromodeoxyuridine staining were markedly enhanced in colons of TG+ mice compared with controls, indicating increased mucosal protection and regeneration.
Conclusions—The significantly reduced susceptibility of mice overexpressing TGF-α to DSS further substantiates that endogenous TGF-α is a pivotal mediator of protection and/or healing mechanisms in the colon.
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