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HMOX1 knockdown reversed the inhibiting effect of KF on TNF-α-induced activation of CCD-18Co cells. (A–C) The transfection <t>efficiency</t> of sh-HMOX1/HMOX1 overexpression plasmids was detected by qRT-PCR/western blot. GAPDH was the internal parameter. (D) The viability of CCD-18Co cells was examined by CCK-8. (E–H) Western blot was used to quantify the levels of activation marker proteins in CCD-18Co cells, including MMP2/9 and α-SMA. GAPDH was the internal parameter. (I–K) The level of FN1, Col1a1 and Col3a1 was detected by qRT-PCR. Each experiment was repeated 3 times. ΔΔΔ P < 0.001 vs. overexpression negative control (OE-NC); θθθ P < 0.001 vs. short hairpin RNA negative control (sh-NC); + P < 0.05, +++ P < 0.001 vs. TNF-α; ψ P < 0.05, ψψ P < 0.01, ψψψ P < 0.001 vs. TNF-ɑ+KF + OE-NC + sh-NC; Ω P < 0.05, ΩΩ P < 0.01, ΩΩΩ P < 0.001 vs.TNF-ɑ+KF; ε P < 0.05, εε P < 0.01, εεε P < 0.001 vs. TNF-ɑ+overexpression (OE)-HMOX1.
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HMOX1 knockdown reversed the inhibiting effect of KF on TNF-α-induced activation of CCD-18Co cells. (A–C) The transfection <t>efficiency</t> of sh-HMOX1/HMOX1 overexpression plasmids was detected by qRT-PCR/western blot. GAPDH was the internal parameter. (D) The viability of CCD-18Co cells was examined by CCK-8. (E–H) Western blot was used to quantify the levels of activation marker proteins in CCD-18Co cells, including MMP2/9 and α-SMA. GAPDH was the internal parameter. (I–K) The level of FN1, Col1a1 and Col3a1 was detected by qRT-PCR. Each experiment was repeated 3 times. ΔΔΔ P < 0.001 vs. overexpression negative control (OE-NC); θθθ P < 0.001 vs. short hairpin RNA negative control (sh-NC); + P < 0.05, +++ P < 0.001 vs. TNF-α; ψ P < 0.05, ψψ P < 0.01, ψψψ P < 0.001 vs. TNF-ɑ+KF + OE-NC + sh-NC; Ω P < 0.05, ΩΩ P < 0.01, ΩΩΩ P < 0.001 vs.TNF-ɑ+KF; ε P < 0.05, εε P < 0.01, εεε P < 0.001 vs. TNF-ɑ+overexpression (OE)-HMOX1.
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HMOX1 knockdown reversed the inhibiting effect of KF on TNF-α-induced activation of CCD-18Co cells. (A–C) The transfection efficiency of sh-HMOX1/HMOX1 overexpression plasmids was detected by qRT-PCR/western blot. GAPDH was the internal parameter. (D) The viability of CCD-18Co cells was examined by CCK-8. (E–H) Western blot was used to quantify the levels of activation marker proteins in CCD-18Co cells, including MMP2/9 and α-SMA. GAPDH was the internal parameter. (I–K) The level of FN1, Col1a1 and Col3a1 was detected by qRT-PCR. Each experiment was repeated 3 times. ΔΔΔ P < 0.001 vs. overexpression negative control (OE-NC); θθθ P < 0.001 vs. short hairpin RNA negative control (sh-NC); + P < 0.05, +++ P < 0.001 vs. TNF-α; ψ P < 0.05, ψψ P < 0.01, ψψψ P < 0.001 vs. TNF-ɑ+KF + OE-NC + sh-NC; Ω P < 0.05, ΩΩ P < 0.01, ΩΩΩ P < 0.001 vs.TNF-ɑ+KF; ε P < 0.05, εε P < 0.01, εεε P < 0.001 vs. TNF-ɑ+overexpression (OE)-HMOX1.

Journal: Frontiers in Pharmacology

Article Title: Kaempferol in inflammatory bowel disease: regulating intestinal epithelial-fibroblast crosstalk

doi: 10.3389/fphar.2026.1799034

Figure Lengend Snippet: HMOX1 knockdown reversed the inhibiting effect of KF on TNF-α-induced activation of CCD-18Co cells. (A–C) The transfection efficiency of sh-HMOX1/HMOX1 overexpression plasmids was detected by qRT-PCR/western blot. GAPDH was the internal parameter. (D) The viability of CCD-18Co cells was examined by CCK-8. (E–H) Western blot was used to quantify the levels of activation marker proteins in CCD-18Co cells, including MMP2/9 and α-SMA. GAPDH was the internal parameter. (I–K) The level of FN1, Col1a1 and Col3a1 was detected by qRT-PCR. Each experiment was repeated 3 times. ΔΔΔ P < 0.001 vs. overexpression negative control (OE-NC); θθθ P < 0.001 vs. short hairpin RNA negative control (sh-NC); + P < 0.05, +++ P < 0.001 vs. TNF-α; ψ P < 0.05, ψψ P < 0.01, ψψψ P < 0.001 vs. TNF-ɑ+KF + OE-NC + sh-NC; Ω P < 0.05, ΩΩ P < 0.01, ΩΩΩ P < 0.001 vs.TNF-ɑ+KF; ε P < 0.05, εε P < 0.01, εεε P < 0.001 vs. TNF-ɑ+overexpression (OE)-HMOX1.

Article Snippet: For the mice in the KF treatment groups, oral gavage of KF (HY-14590, MCE, United States) was initiated on the first day of DSS treatment, with daily doses of 25 mg/kg (low), 50 mg/kg (medium), or 100 mg/kg (high) ( ).

Techniques: Knockdown, Activation Assay, Transfection, Over Expression, Quantitative RT-PCR, Western Blot, CCK-8 Assay, Marker, Negative Control, shRNA