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Jackson Laboratory female il 12β knockout
<t>Cardiac</t> <t>IL-12β</t> expression was significantly increased after TAC. (A) Western blots and quantified data of LV IL-12β expression in WT sham and WT TAC mice. (B) Representative LV IL-12β staining images and quantified data of IL-12β + area. (C) Representative images of IL-12β and CD45 co-immunostaining of WT mice LV tissue under sham and TAC conditions. The green stain in panel B is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5 per group.
Female Il 12β Knockout, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/female+il+12%CE%B2+knockout/12%CE%B2+female+il+knockout/pmc12927108-37-6-9
Average 86 stars, based on 1 article reviews
female il 12β knockout - by Bioz Stars, 2026-09
86/100 stars

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1) Product Images from "Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development"

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

Journal: Redox Biology

doi: 10.1016/j.redox.2026.104082

Cardiac IL-12β expression was significantly increased after TAC. (A) Western blots and quantified data of LV IL-12β expression in WT sham and WT TAC mice. (B) Representative LV IL-12β staining images and quantified data of IL-12β + area. (C) Representative images of IL-12β and CD45 co-immunostaining of WT mice LV tissue under sham and TAC conditions. The green stain in panel B is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5 per group.
Figure Legend Snippet: Cardiac IL-12β expression was significantly increased after TAC. (A) Western blots and quantified data of LV IL-12β expression in WT sham and WT TAC mice. (B) Representative LV IL-12β staining images and quantified data of IL-12β + area. (C) Representative images of IL-12β and CD45 co-immunostaining of WT mice LV tissue under sham and TAC conditions. The green stain in panel B is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5 per group.

Techniques Used: Expressing, Western Blot, Staining, Immunostaining

IL-12β KO significantly attenuated TAC-induced cardiac dysfunction, an increase in LV weight, LA weight, lung weight, and RV weight in male and female mice. (A) Representative M-mode echocardiographic images of WT and IL-12β KO male mice: pre-TAC, 2 weeks, 4 weeks, and 6 weeks after TAC, and Quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of both sexes. (B) Survival curves of WT TAC and IL-12β KO TAC mice of both sexes (log-rank test). (C–F) The ratio of LV weight, left atrial (LA) weight, lung weight, RV weight to tibial length (TL) of the indicated groups. (G) Representative LV WGA staining images and quantified data of cardiomyocyte cross-sectional areas. ∗p < 0.05; # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 7 to 22 per group for panels A-F and n = 4-5 per group for panel G; LVEF, LV ejection fraction; LVFS, LV fractional shortening; LVESD, LV end-systolic diameter; LVEDD, LV end-diastolic diameter.
Figure Legend Snippet: IL-12β KO significantly attenuated TAC-induced cardiac dysfunction, an increase in LV weight, LA weight, lung weight, and RV weight in male and female mice. (A) Representative M-mode echocardiographic images of WT and IL-12β KO male mice: pre-TAC, 2 weeks, 4 weeks, and 6 weeks after TAC, and Quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of both sexes. (B) Survival curves of WT TAC and IL-12β KO TAC mice of both sexes (log-rank test). (C–F) The ratio of LV weight, left atrial (LA) weight, lung weight, RV weight to tibial length (TL) of the indicated groups. (G) Representative LV WGA staining images and quantified data of cardiomyocyte cross-sectional areas. ∗p < 0.05; # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 7 to 22 per group for panels A-F and n = 4-5 per group for panel G; LVEF, LV ejection fraction; LVFS, LV fractional shortening; LVESD, LV end-systolic diameter; LVEDD, LV end-diastolic diameter.

Techniques Used: Staining

IL-12β KO attenuated TAC-induced alterations in the gene expression related to fibrosis and inflammation (A) Principal component analysis of WT and IL-12β KO mice, under sham or TAC conditions. (B) Venn diagram showing differentially expressed genes (DEGs) of WT and IL-12β KO mice under sham or TAC conditions, as well as the shared and uniquely changed genes. (C) DEGs cluster heatmap in WT mice compared to IL-12β KO mice, under sham or TAC conditions. (D) Volcano plots showing upregulated and downregulated genes among the groups. (E) Gene ontology (GO) biological processes enrichment bubble chart in WT TAC mice compared to IL-12β KO TAC. (F) GO cellular components enrichment histogram shows the enriched cellular components between KO and WT mice after TAC. n = 2 per group for sham and n = 3 per group for TAC.
Figure Legend Snippet: IL-12β KO attenuated TAC-induced alterations in the gene expression related to fibrosis and inflammation (A) Principal component analysis of WT and IL-12β KO mice, under sham or TAC conditions. (B) Venn diagram showing differentially expressed genes (DEGs) of WT and IL-12β KO mice under sham or TAC conditions, as well as the shared and uniquely changed genes. (C) DEGs cluster heatmap in WT mice compared to IL-12β KO mice, under sham or TAC conditions. (D) Volcano plots showing upregulated and downregulated genes among the groups. (E) Gene ontology (GO) biological processes enrichment bubble chart in WT TAC mice compared to IL-12β KO TAC. (F) GO cellular components enrichment histogram shows the enriched cellular components between KO and WT mice after TAC. n = 2 per group for sham and n = 3 per group for TAC.

Techniques Used: Gene Expression

IL-12β KO suppressed LV genetic pathways associated with extracellular matrix remodeling, inflammation, and LV fibrosis in mice after TAC. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC, identified by GSEA with ReactomeGSA. (B) Representative GSEA plots of collagen formation and extracellular matrix organization. (C, D) Representative images and quantified data of LV interstitial and perivascular fibrosis performed by Sirius Red/Fast Green staining in male and female mice. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 3 per group for panels A-B and n = 4-5 per group for panel D.
Figure Legend Snippet: IL-12β KO suppressed LV genetic pathways associated with extracellular matrix remodeling, inflammation, and LV fibrosis in mice after TAC. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC, identified by GSEA with ReactomeGSA. (B) Representative GSEA plots of collagen formation and extracellular matrix organization. (C, D) Representative images and quantified data of LV interstitial and perivascular fibrosis performed by Sirius Red/Fast Green staining in male and female mice. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 3 per group for panels A-B and n = 4-5 per group for panel D.

Techniques Used: Staining

IL-12β KO significantly attenuated TAC-induced LV inflammation in mice. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC were identified by GSEA with KEGG pathway analysis. (B) Heatmap shows the top LV immune and/or inflammation-related genes in KO and WT mice after TAC. (C, D) Representative LV CD45 + immuno-staining images and quantified data of LV CD45 + of the indicated groups. (E) Percentage distribution of major immune cell subsets within LV CD45 + cells of the indicated groups determined by flow cytometry. The green stain in panel C is due to cardiac autofluorescence recorded at FITC channel. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 2-3 per group for panels A-B and n = 4-5 per group for panels D-E.
Figure Legend Snippet: IL-12β KO significantly attenuated TAC-induced LV inflammation in mice. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC were identified by GSEA with KEGG pathway analysis. (B) Heatmap shows the top LV immune and/or inflammation-related genes in KO and WT mice after TAC. (C, D) Representative LV CD45 + immuno-staining images and quantified data of LV CD45 + of the indicated groups. (E) Percentage distribution of major immune cell subsets within LV CD45 + cells of the indicated groups determined by flow cytometry. The green stain in panel C is due to cardiac autofluorescence recorded at FITC channel. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 2-3 per group for panels A-B and n = 4-5 per group for panels D-E.

Techniques Used: Immunostaining, Flow Cytometry, Staining

IL-12β KO attenuated TAC-induced pulmonary inflammation, fibrosis, and vessel remodeling in male and female mice. (A, B) Representative images and quantified data of infiltrated CD45 + leukocytes in the lung performed by immuno-histological staining. (C, D) Representative images and quantified data of lung fibrosis performed by Sirius Red/Fast Green staining. (E, F) Representative images and quantified data of lung vessel remodeling performed by immuno-histological staining. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 4-5 per group.
Figure Legend Snippet: IL-12β KO attenuated TAC-induced pulmonary inflammation, fibrosis, and vessel remodeling in male and female mice. (A, B) Representative images and quantified data of infiltrated CD45 + leukocytes in the lung performed by immuno-histological staining. (C, D) Representative images and quantified data of lung fibrosis performed by Sirius Red/Fast Green staining. (E, F) Representative images and quantified data of lung vessel remodeling performed by immuno-histological staining. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 4-5 per group.

Techniques Used: Staining

IL-12β KO significantly attenuated TAC-induced early-phase LV dysfunction, cardiomyocyte hypertrophy, and inflammation. (A) Representative M-mode echocardiographic images and quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of the indicated groups. (B) The ratios of cardiac and pulmonary tissues to tibial length (TL) of the indicated groups. (C, D) Representative images and quantified data of LV cardiomyocyte size and LV CD45 + cells of the indicated groups. (E) Percentage of major immune cell subsets within LV CD45 + cells determined by flow cytometry. (F) Representative flow cytometry plots and quantified data of CD44 + CD3 + , CD44 + CD4 + , and CD44 + CD8 + T cells within the corresponding T cells. The green stain in panel D is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5-10 per group.
Figure Legend Snippet: IL-12β KO significantly attenuated TAC-induced early-phase LV dysfunction, cardiomyocyte hypertrophy, and inflammation. (A) Representative M-mode echocardiographic images and quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of the indicated groups. (B) The ratios of cardiac and pulmonary tissues to tibial length (TL) of the indicated groups. (C, D) Representative images and quantified data of LV cardiomyocyte size and LV CD45 + cells of the indicated groups. (E) Percentage of major immune cell subsets within LV CD45 + cells determined by flow cytometry. (F) Representative flow cytometry plots and quantified data of CD44 + CD3 + , CD44 + CD4 + , and CD44 + CD8 + T cells within the corresponding T cells. The green stain in panel D is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5-10 per group.

Techniques Used: Flow Cytometry, Staining

IL-12β KO significantly attenuated
Figure Legend Snippet: IL-12β KO significantly attenuated "stem cell-like" central memory T cell activation and their IFNγ production in the drainage lymph nodes. (A, B) Percentages of major immune cell subsets within CD45 + cells in the drainage lymph nodes determined by flow cytometry. (C) Percentages of IFNγ + CD8 + and TNFα + CD8 + within CD8 + T cells. (D, E) Percentages of CXCR3 + CD4 + and CXCR3 + CD8 + T cells within CD4 + and CD8 + T cells, respectively. (F) Percentage of effective memory (CD44 + CD62L − ), naïve (CD44 − CD62L + ), and central memory (CD44 + CD62L + ) T cells of CD8 + T cells. ∗p < 0.05; T EM , Effective Memory T Cells; T naïve , Naïve T Cells; T CM , Central Memory T Cells; n = 4-5 per group.

Techniques Used: Activation Assay, Flow Cytometry

IL-12β KO and anti-IL-12β antibody treatment significantly attenuated TAC-induced LV oxidative stress. (A) Representative dihydroethidium (DHE) staining images and quantified data of DHE intensity of the indicated groups. (B) Representative western blots and quantification of LV 3-nitrotyrosine (3-NT) and 4-hydroxynonenal (4-HNE) of the indicated groups. (C-E) Representative DHE, 3-NT, and 4-HNE staining images, and quantified data of relative DHE, 3-NT, and 4-HNE intensity of the indicated groups. ∗p < 0.05; n = 5 to 6 per group.
Figure Legend Snippet: IL-12β KO and anti-IL-12β antibody treatment significantly attenuated TAC-induced LV oxidative stress. (A) Representative dihydroethidium (DHE) staining images and quantified data of DHE intensity of the indicated groups. (B) Representative western blots and quantification of LV 3-nitrotyrosine (3-NT) and 4-hydroxynonenal (4-HNE) of the indicated groups. (C-E) Representative DHE, 3-NT, and 4-HNE staining images, and quantified data of relative DHE, 3-NT, and 4-HNE intensity of the indicated groups. ∗p < 0.05; n = 5 to 6 per group.

Techniques Used: Staining, Western Blot

Related Articles

Mouse Assay:

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development
Article Snippet: .. Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis. ..

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development.
Article Snippet: .. Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis. ..

Knock-Out:

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development
Article Snippet: .. Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis. ..

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development.
Article Snippet: .. Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis. ..



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Jackson Laboratory female il 12β knockout
<t>Cardiac</t> <t>IL-12β</t> expression was significantly increased after TAC. (A) Western blots and quantified data of LV IL-12β expression in WT sham and WT TAC mice. (B) Representative LV IL-12β staining images and quantified data of IL-12β + area. (C) Representative images of IL-12β and CD45 co-immunostaining of WT mice LV tissue under sham and TAC conditions. The green stain in panel B is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5 per group.
Female Il 12β Knockout, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/female+il+12%CE%B2+knockout/12%CE%B2+female+il+knockout/pmc12927108-37-6-9
Average 86 stars, based on 1 article reviews
female il 12β knockout - by Bioz Stars, 2026-09
86/100 stars
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Cardiac IL-12β expression was significantly increased after TAC. (A) Western blots and quantified data of LV IL-12β expression in WT sham and WT TAC mice. (B) Representative LV IL-12β staining images and quantified data of IL-12β + area. (C) Representative images of IL-12β and CD45 co-immunostaining of WT mice LV tissue under sham and TAC conditions. The green stain in panel B is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5 per group.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: Cardiac IL-12β expression was significantly increased after TAC. (A) Western blots and quantified data of LV IL-12β expression in WT sham and WT TAC mice. (B) Representative LV IL-12β staining images and quantified data of IL-12β + area. (C) Representative images of IL-12β and CD45 co-immunostaining of WT mice LV tissue under sham and TAC conditions. The green stain in panel B is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5 per group.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Expressing, Western Blot, Staining, Immunostaining

IL-12β KO significantly attenuated TAC-induced cardiac dysfunction, an increase in LV weight, LA weight, lung weight, and RV weight in male and female mice. (A) Representative M-mode echocardiographic images of WT and IL-12β KO male mice: pre-TAC, 2 weeks, 4 weeks, and 6 weeks after TAC, and Quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of both sexes. (B) Survival curves of WT TAC and IL-12β KO TAC mice of both sexes (log-rank test). (C–F) The ratio of LV weight, left atrial (LA) weight, lung weight, RV weight to tibial length (TL) of the indicated groups. (G) Representative LV WGA staining images and quantified data of cardiomyocyte cross-sectional areas. ∗p < 0.05; # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 7 to 22 per group for panels A-F and n = 4-5 per group for panel G; LVEF, LV ejection fraction; LVFS, LV fractional shortening; LVESD, LV end-systolic diameter; LVEDD, LV end-diastolic diameter.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO significantly attenuated TAC-induced cardiac dysfunction, an increase in LV weight, LA weight, lung weight, and RV weight in male and female mice. (A) Representative M-mode echocardiographic images of WT and IL-12β KO male mice: pre-TAC, 2 weeks, 4 weeks, and 6 weeks after TAC, and Quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of both sexes. (B) Survival curves of WT TAC and IL-12β KO TAC mice of both sexes (log-rank test). (C–F) The ratio of LV weight, left atrial (LA) weight, lung weight, RV weight to tibial length (TL) of the indicated groups. (G) Representative LV WGA staining images and quantified data of cardiomyocyte cross-sectional areas. ∗p < 0.05; # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 7 to 22 per group for panels A-F and n = 4-5 per group for panel G; LVEF, LV ejection fraction; LVFS, LV fractional shortening; LVESD, LV end-systolic diameter; LVEDD, LV end-diastolic diameter.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Staining

IL-12β KO attenuated TAC-induced alterations in the gene expression related to fibrosis and inflammation (A) Principal component analysis of WT and IL-12β KO mice, under sham or TAC conditions. (B) Venn diagram showing differentially expressed genes (DEGs) of WT and IL-12β KO mice under sham or TAC conditions, as well as the shared and uniquely changed genes. (C) DEGs cluster heatmap in WT mice compared to IL-12β KO mice, under sham or TAC conditions. (D) Volcano plots showing upregulated and downregulated genes among the groups. (E) Gene ontology (GO) biological processes enrichment bubble chart in WT TAC mice compared to IL-12β KO TAC. (F) GO cellular components enrichment histogram shows the enriched cellular components between KO and WT mice after TAC. n = 2 per group for sham and n = 3 per group for TAC.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO attenuated TAC-induced alterations in the gene expression related to fibrosis and inflammation (A) Principal component analysis of WT and IL-12β KO mice, under sham or TAC conditions. (B) Venn diagram showing differentially expressed genes (DEGs) of WT and IL-12β KO mice under sham or TAC conditions, as well as the shared and uniquely changed genes. (C) DEGs cluster heatmap in WT mice compared to IL-12β KO mice, under sham or TAC conditions. (D) Volcano plots showing upregulated and downregulated genes among the groups. (E) Gene ontology (GO) biological processes enrichment bubble chart in WT TAC mice compared to IL-12β KO TAC. (F) GO cellular components enrichment histogram shows the enriched cellular components between KO and WT mice after TAC. n = 2 per group for sham and n = 3 per group for TAC.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Gene Expression

IL-12β KO suppressed LV genetic pathways associated with extracellular matrix remodeling, inflammation, and LV fibrosis in mice after TAC. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC, identified by GSEA with ReactomeGSA. (B) Representative GSEA plots of collagen formation and extracellular matrix organization. (C, D) Representative images and quantified data of LV interstitial and perivascular fibrosis performed by Sirius Red/Fast Green staining in male and female mice. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 3 per group for panels A-B and n = 4-5 per group for panel D.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO suppressed LV genetic pathways associated with extracellular matrix remodeling, inflammation, and LV fibrosis in mice after TAC. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC, identified by GSEA with ReactomeGSA. (B) Representative GSEA plots of collagen formation and extracellular matrix organization. (C, D) Representative images and quantified data of LV interstitial and perivascular fibrosis performed by Sirius Red/Fast Green staining in male and female mice. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 3 per group for panels A-B and n = 4-5 per group for panel D.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Staining

IL-12β KO significantly attenuated TAC-induced LV inflammation in mice. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC were identified by GSEA with KEGG pathway analysis. (B) Heatmap shows the top LV immune and/or inflammation-related genes in KO and WT mice after TAC. (C, D) Representative LV CD45 + immuno-staining images and quantified data of LV CD45 + of the indicated groups. (E) Percentage distribution of major immune cell subsets within LV CD45 + cells of the indicated groups determined by flow cytometry. The green stain in panel C is due to cardiac autofluorescence recorded at FITC channel. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 2-3 per group for panels A-B and n = 4-5 per group for panels D-E.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO significantly attenuated TAC-induced LV inflammation in mice. (A) The top 20 upregulated and downregulated pathways between KO and WT mice after TAC were identified by GSEA with KEGG pathway analysis. (B) Heatmap shows the top LV immune and/or inflammation-related genes in KO and WT mice after TAC. (C, D) Representative LV CD45 + immuno-staining images and quantified data of LV CD45 + of the indicated groups. (E) Percentage distribution of major immune cell subsets within LV CD45 + cells of the indicated groups determined by flow cytometry. The green stain in panel C is due to cardiac autofluorescence recorded at FITC channel. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 2-3 per group for panels A-B and n = 4-5 per group for panels D-E.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Immunostaining, Flow Cytometry, Staining

IL-12β KO attenuated TAC-induced pulmonary inflammation, fibrosis, and vessel remodeling in male and female mice. (A, B) Representative images and quantified data of infiltrated CD45 + leukocytes in the lung performed by immuno-histological staining. (C, D) Representative images and quantified data of lung fibrosis performed by Sirius Red/Fast Green staining. (E, F) Representative images and quantified data of lung vessel remodeling performed by immuno-histological staining. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 4-5 per group.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO attenuated TAC-induced pulmonary inflammation, fibrosis, and vessel remodeling in male and female mice. (A, B) Representative images and quantified data of infiltrated CD45 + leukocytes in the lung performed by immuno-histological staining. (C, D) Representative images and quantified data of lung fibrosis performed by Sirius Red/Fast Green staining. (E, F) Representative images and quantified data of lung vessel remodeling performed by immuno-histological staining. # p < 0.05 compared to WT sham; † p < 0.05 compared to WT TAC; $ p < 0.05 compared to IL-12β KO sham; n = 4-5 per group.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Staining

IL-12β KO significantly attenuated TAC-induced early-phase LV dysfunction, cardiomyocyte hypertrophy, and inflammation. (A) Representative M-mode echocardiographic images and quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of the indicated groups. (B) The ratios of cardiac and pulmonary tissues to tibial length (TL) of the indicated groups. (C, D) Representative images and quantified data of LV cardiomyocyte size and LV CD45 + cells of the indicated groups. (E) Percentage of major immune cell subsets within LV CD45 + cells determined by flow cytometry. (F) Representative flow cytometry plots and quantified data of CD44 + CD3 + , CD44 + CD4 + , and CD44 + CD8 + T cells within the corresponding T cells. The green stain in panel D is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5-10 per group.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO significantly attenuated TAC-induced early-phase LV dysfunction, cardiomyocyte hypertrophy, and inflammation. (A) Representative M-mode echocardiographic images and quantified data of echocardiographic measurements of LVEF, LVFS, LVESD, and LVEDD of the indicated groups. (B) The ratios of cardiac and pulmonary tissues to tibial length (TL) of the indicated groups. (C, D) Representative images and quantified data of LV cardiomyocyte size and LV CD45 + cells of the indicated groups. (E) Percentage of major immune cell subsets within LV CD45 + cells determined by flow cytometry. (F) Representative flow cytometry plots and quantified data of CD44 + CD3 + , CD44 + CD4 + , and CD44 + CD8 + T cells within the corresponding T cells. The green stain in panel D is due to cardiac autofluorescence recorded at FITC channel. ∗p < 0.05; n = 5-10 per group.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Flow Cytometry, Staining

IL-12β KO significantly attenuated

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO significantly attenuated "stem cell-like" central memory T cell activation and their IFNγ production in the drainage lymph nodes. (A, B) Percentages of major immune cell subsets within CD45 + cells in the drainage lymph nodes determined by flow cytometry. (C) Percentages of IFNγ + CD8 + and TNFα + CD8 + within CD8 + T cells. (D, E) Percentages of CXCR3 + CD4 + and CXCR3 + CD8 + T cells within CD4 + and CD8 + T cells, respectively. (F) Percentage of effective memory (CD44 + CD62L − ), naïve (CD44 − CD62L + ), and central memory (CD44 + CD62L + ) T cells of CD8 + T cells. ∗p < 0.05; T EM , Effective Memory T Cells; T naïve , Naïve T Cells; T CM , Central Memory T Cells; n = 4-5 per group.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Activation Assay, Flow Cytometry

IL-12β KO and anti-IL-12β antibody treatment significantly attenuated TAC-induced LV oxidative stress. (A) Representative dihydroethidium (DHE) staining images and quantified data of DHE intensity of the indicated groups. (B) Representative western blots and quantification of LV 3-nitrotyrosine (3-NT) and 4-hydroxynonenal (4-HNE) of the indicated groups. (C-E) Representative DHE, 3-NT, and 4-HNE staining images, and quantified data of relative DHE, 3-NT, and 4-HNE intensity of the indicated groups. ∗p < 0.05; n = 5 to 6 per group.

Journal: Redox Biology

Article Title: Genetic inhibition of IL-12β suppresses systolic overload-induced cardiac oxidative stress, inflammation, and heart failure development

doi: 10.1016/j.redox.2026.104082

Figure Lengend Snippet: IL-12β KO and anti-IL-12β antibody treatment significantly attenuated TAC-induced LV oxidative stress. (A) Representative dihydroethidium (DHE) staining images and quantified data of DHE intensity of the indicated groups. (B) Representative western blots and quantification of LV 3-nitrotyrosine (3-NT) and 4-hydroxynonenal (4-HNE) of the indicated groups. (C-E) Representative DHE, 3-NT, and 4-HNE staining images, and quantified data of relative DHE, 3-NT, and 4-HNE intensity of the indicated groups. ∗p < 0.05; n = 5 to 6 per group.

Article Snippet: Mice and Experimental Protocols: Male and female IL-12β knockout (Jackson Laboratory, Strain #002693) and wild-type (WT) C57BL/6J (Jackson Laboratory, Strain #000664) mice were subjected to sham or transverse aortic constriction (TAC) surgery, a procedure used to replicate clinical conditions such as hypertension and aortic stenosis.

Techniques: Staining, Western Blot