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. Author manuscript; available in PMC: 2024 Dec 9.
Published in final edited form as: Cell Rep. 2019 Dec 10;29(11):3522–3538.e7. doi: 10.1016/j.celrep.2019.11.028

Figure 4. SENP7 Suppression Ameliorates DSS Induced Colitis.

Figure 4

(A) Schematic representation of knockdown of SENP7 in mice. SENP7 morpholino was injected intraperitoneally (day 0) and on day 4, followed by euthanasia and tissue isolation (n = 3).

(B) Mouse body weight (C, untreated control; C-MO, negative control; Mo-SENP7KD, SENP7 knockdown; DSS7, 7 days of DSS treatment; DSS7-Mo-SENP7KD, SENP7 knockdown with 7 days of DSS treatment).

(C) Gross morphology of the colon.

(D) Immunoblot showing protein expression of SIAH2, SENP7, and SUMO2/3 from isolated intestinal epithelial cells. Densitometry analysis by means + SEM from three independent experiments (right panel).

(E) Immunoblot showing SENP7 expression in splenocytes of the indicated group. Actin was used as a loading control in (D) and (E). Densitometry analysis by means + SEM from three independent experiments (right panel).

(F) Histopathology along with scores (lower panel) of colonic sections.

(G–L) ELISAs of mucosal isolates from the intestines of mice: IFN-γ (G), TNF-α (H), IL-17 (I), TGF-β (J), IL-10 (K), and TSLP (L) (n = 3 mice). Data are presented as mean + SEM.

(M) Bar graphs showing frequency of γδ T cells in presence of morpholino-mediated SENP7 knockdown in DSS and recovery groups in MLNs and spleen.

(N) Histogram overlay for γδ T frequency for the above groups. Statistical significance was calculated using a one-way ANOVA with Tukey’s posttest.

*p < 0.05; **p < 0.01; ***p < 0.001; ns, non-significant. See also Figures S3–S5.