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A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and <t>K14;</t> proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.
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A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and <t>K14;</t> proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.
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A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and <t>K14;</t> proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.
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A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and <t>K14;</t> proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.
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A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and <t>K14;</t> proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.
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A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and K14; proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.

Journal: Cell Death Discovery

Article Title: 4-aminopyridine attenuates inflammation and apoptosis and increases angiogenesis to promote skin regeneration following a burn injury in mice

doi: 10.1038/s41420-024-02199-6

Figure Lengend Snippet: A, B Representative images and quantitative results of IF staining of keratinocyte markers (K10; terminal differentiation and K14; proliferative) in saline and 4-AP treated skin burn tissues on days 3 and 7. Scale bar = 100 µm. n = 4 skin tissues per group. C , D Western blotting and ( E ) qRT-PCR quantitative results show that 4-AP treatment significantly increased keratin markers protein and gene (K10 and K14) expressions compared to the saline group on days 3 and 7. n = 3 skin tissues per group. Data are represented as mean ± SEM. The statistical significance is indicated by asterisks (* P < 0.05, ** P < 0.0021, and *** P < 0.0002 vs. saline group) and compared using two-tailed, unpaired t-tests.

Article Snippet: Next, primary antibody staining was performed with CD31 (1:100, # 553370, BD Pharmingen), IL1β (1:250, # GTX74034, GeneTex), CD206 (1:400, # 141703, BioLegend), F4/80 (1:500, # SAB4501656, Sigma Aldrich), K10 (1:100, # SAB4501656, Sigma Aldrich), K14 (1:100, # NBP2-34270, Novus Biologicals), Vimentin (1:200, # 10366-1-AP, Thermo Fisher Scientific), and α-SMA (1:500, # 14-9760-82, Thermo Fisher Scientific) at 4 °C overnight incubation.

Techniques: Staining, Saline, Western Blot, Quantitative RT-PCR, Two Tailed Test