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Immunohistochemical staining of the inflammatory factors <t>TNF‐α</t> and IL‐1β in diabetic wounds. (a) Immunohistochemical staining of TNF‐α in diabetic wounds under different treatments. (b) Immunohistochemical staining of IL‐1β of diabetic wounds under different treatments. (c) Statistical analysis of the percentage of TNF‐α‐ and IL‐1β‐positive area in wound tissue ( n = 4). The data are expressed as mean ± SD. * p < 0.05, ** p < 0.01, n.s., no significance (one‐way ANOVA). <t>IL,</t> <t>interleukin;</t> TNF, tumor necrosis factor.
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Immunohistochemical staining of the inflammatory factors <t>TNF‐α</t> and IL‐1β in diabetic wounds. (a) Immunohistochemical staining of TNF‐α in diabetic wounds under different treatments. (b) Immunohistochemical staining of IL‐1β of diabetic wounds under different treatments. (c) Statistical analysis of the percentage of TNF‐α‐ and IL‐1β‐positive area in wound tissue ( n = 4). The data are expressed as mean ± SD. * p < 0.05, ** p < 0.01, n.s., no significance (one‐way ANOVA). <t>IL,</t> <t>interleukin;</t> TNF, tumor necrosis factor.
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Immunohistochemical staining of the inflammatory factors TNF‐α and IL‐1β in diabetic wounds. (a) Immunohistochemical staining of TNF‐α in diabetic wounds under different treatments. (b) Immunohistochemical staining of IL‐1β of diabetic wounds under different treatments. (c) Statistical analysis of the percentage of TNF‐α‐ and IL‐1β‐positive area in wound tissue ( n = 4). The data are expressed as mean ± SD. * p < 0.05, ** p < 0.01, n.s., no significance (one‐way ANOVA). IL, interleukin; TNF, tumor necrosis factor.

Journal: Bioengineering & Translational Medicine

Article Title: Self‐assembly of PEG – PPS polymers and LL ‐37 peptide nanomicelles improves the oxidative microenvironment and promotes angiogenesis to facilitate chronic wound healing

doi: 10.1002/btm2.10619

Figure Lengend Snippet: Immunohistochemical staining of the inflammatory factors TNF‐α and IL‐1β in diabetic wounds. (a) Immunohistochemical staining of TNF‐α in diabetic wounds under different treatments. (b) Immunohistochemical staining of IL‐1β of diabetic wounds under different treatments. (c) Statistical analysis of the percentage of TNF‐α‐ and IL‐1β‐positive area in wound tissue ( n = 4). The data are expressed as mean ± SD. * p < 0.05, ** p < 0.01, n.s., no significance (one‐way ANOVA). IL, interleukin; TNF, tumor necrosis factor.

Article Snippet: After first incubating the tissue sections with primary antibodies (rabbit anti‐mouse CD31 [1:50, ABclonal, Cat# A0378], anti‐interleukin (IL)‐1 beta rabbit pAb [1:800, Servicebio, GB11113‐100], and tumor necrosis factor (TNF) Alpha [1:400, Proteintech, Cat No. 60291‐1‐lg]) at 4°C for 24 h, the sections were incubated with biotin‐labeled secondary antibody and horseradish enzyme‐labeled streptomyces at room temperature for 2 h. The color reaction was performed using diaminobenzidine (DAB) kit.

Techniques: Immunohistochemistry, Staining