p jak  (Proteintech)

Journal: CytoJournal

Article Title: Mapping the function of EF-hand domain-containing protein 2 and determining its clinical relevance in non-small-cell lung cancer through single-cell transcriptomics

doi: 10.25259/Cytojournal_29_2025

Figure Lengend Snippet: EFHD2 influences lung cancer cell proliferation, apoptosis, migration, invasion, and various signaling pathways. (a) WB analysis depicting EFHD2 protein expression in normal bronchial epithelial cells (BEAS-2B) and different lung cancer cell lines (A549, NCI-H1299, and HCC827). (b) Relative mRNA levels of EFHD2 in BEAS-2B and lung cancer cell lines, quantified through qRT-PCR. The data are presented as mean ± SD. (c) WB illustrating EFHD2 protein expression levels. (d) qRT-PCR analysis of EFHD2 mRNA expression. (e) CCK-8 assay assessing the impact of EFHD2 OE and KD on cell proliferation; data were presented as OD450 values over 72 h. (f) Flow cytometry analysis evaluating apoptosis rates. (g) Transwell migration and invasion assays. (h) Colony formation assay. (i) WB analysis of JAK and STAT protein expression, using GAPDH as a loading control. Data are expressed as mean ± SD. ✶ P < 0.05, ✶ ✶ P < 0.01, ✶ ✶ ✶ P < 0.001 compared with the A549 group; # P < 0.05, ## P < 0.01, ### P < 0.001 compared with the NCI-H1299 group. The scale bar represents 100 µm. EFHD2: EF-hand domain-containing protein 2, WB: Western blot, JAK: Janus Kinase, STAT: Signal transducers and activators of transcription, GAPDH: Glyceraldehyde 3-phosphate dehydrogenase, qRT-PCR: Quantitative real-time polymerase chain reaction, CCK-8: Cell counting kit 8, OE: Overexpression, KD: Knockdown, mRNA: Messenger RNA, OD450: Optical density at 450 nm, SD: Standard deviation.

Article Snippet: The membranes were then exposed overnight at 4°C to primary antibodies targeting EFHD2 (1:1000, ab24368, Abcam, China), JAK1 (1:1000, HY- P80196 , MedChemExpress, China), phospho-JAK (p-JAK) (1:1000, ab138005, Abcam, China), signal transducers and activators of transcription 3 (STAT3) (1:1000, ab68153, Abcam, China), and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (1:1000, ab8245, Abcam, China) (loading control).

Techniques: Migration, Protein-Protein interactions, Expressing, Quantitative RT-PCR, CCK-8 Assay, Flow Cytometry, Colony Assay, Control, Western Blot, Real-time Polymerase Chain Reaction, Cell Counting, Over Expression, Knockdown, Standard Deviation

Journal: CytoJournal

Article Title: Mapping the function of EF-hand domain-containing protein 2 and determining its clinical relevance in non-small-cell lung cancer through single-cell transcriptomics

doi: 10.25259/Cytojournal_29_2025

Figure Lengend Snippet: EFHD2 regulates cell proliferation, migration, invasion, apoptosis, and JAK/STAT signaling. (a) Co-IP identified that FLAG-EFHD2 interacted with Myc-JAK1 in A549+EFHD2 OE and NCI-H1299+EFHD2 KD cells. (b) CCK-8 detected cell proliferation. Inhibition of JAK decreased the proliferation of A549+EFHD2 OE cells, while activation of JAK increased the proliferation of NCI-H1299+EFHD2 KD cells. (c) Flow cytometry to detect apoptosis. Inhibition of JAK increased the apoptosis of A549+EFHD2 OE cells, whereas JAK agonist enhanced the apoptosis of NCI-H1299+EFHD2 KD cells. (d) Transwell migration and invasion. Inhibition of JAK reduced the migration and invasion of A549+EFHD2 OE cells, whereas activation of JAK promoted the migration and invasion of NCI-H1299+EFHD2 KD cells. (e) Colony formation assay. Inhibition of JAK decreased the colony formation of A549+EFHD2 OE cells, whereas activation of JAK enhanced the colony formation of NCI-H1299+EFHD2 KD cells. (f) Western blotting. JAK inhibition decreased the levels of p-JAK1 and p-STAT3 in A549+EFHD2 OE cells, whereas JAK activation increased the levels of p-JAK1 and p-STAT3 in NCI-H1299+EFHD2 KD cells. Data are expressed as mean ± SD. ✶ P < 0.05, ✶ ✶ P < 0.01, ✶ ✶ ✶ P < 0.001 compared with the A549 group; # P < 0.05, ## P < 0.01, ### P < 0.001 compared with the NCI-H1299 group. The scale bar represents 100 µm. JAK: Janus Kinase, STAT: Signal transducers and activators of transcription, Co-IP: Co-immunoprecipitation, EFHD2: EF-hand domain-containing protein 2, OE: Overexpression, KD: Knockdown, CCK-8: Cell counting kit 8, p-JAK: Phospho Janus Kinase, p-STAT: Phospho signal transducers and activators of transcription, SD: Standard deviation.

Article Snippet: The membranes were then exposed overnight at 4°C to primary antibodies targeting EFHD2 (1:1000, ab24368, Abcam, China), JAK1 (1:1000, HY- P80196 , MedChemExpress, China), phospho-JAK (p-JAK) (1:1000, ab138005, Abcam, China), signal transducers and activators of transcription 3 (STAT3) (1:1000, ab68153, Abcam, China), and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (1:1000, ab8245, Abcam, China) (loading control).

Techniques: Migration, Co-Immunoprecipitation Assay, CCK-8 Assay, Inhibition, Activation Assay, Flow Cytometry, Colony Assay, Western Blot, Immunoprecipitation, Over Expression, Knockdown, Cell Counting, Standard Deviation

Journal: Advanced Science

Article Title: 12‐HETE is an Endogenous Modulator of BLT2 Triggering Vascular Degeneration, Dissection, and Rupture

doi: 10.1002/advs.202515897

Figure Lengend Snippet: IL‐6 induced VSMC phenotypic switch through JAK/STAT signal pathway. A) UMAP plot of single‐cell clustering, showing the spatial distribution of different cell types (B cells, endothelial cells, fibroblasts, macrophages, smooth muscle cells, neutrophils, natural killer cells, and proliferating cells). B,C) UMAP plots of subpopulations of macrophages (MAC) and smooth muscle cells (SMC), with macrophages divided into MAC1 to MAC8 subpopulations and smooth muscle cells divided into SMC1 to SMC6 subpopulations. D) Proportional changes in macrophage and smooth muscle cell subpopulations across different groups, illustrating the relative differences in subpopulation proportions between the Control group and the TAD group. E) Differences in cell–cell communication between MAC1, MAC3 clusters and SMC1, SMC3, SMC4 clusters in the Control and TAD groups. Green and red arrows represent communication interactions between different cell clusters, with arrow thickness indicating communication strength. F) Differential expression of IL‐6 in macrophage and smooth muscle cell subpopulations, showing IL‐6 expression levels and statistical significance across different subpopulations in the Control and TAD groups. G) Representative confocal images of αSMA (green) in vascular smooth muscle cells and primary smooth muscle cells. (scale bar, 20 µm). H,I) Quantification of αSMA levels from confocal images ( n = 6 per group). J) Representative Western blot images of p‐JAK, JAK, p‐STAT, STAT, αSMA, and SM22α in primary VSMCs. K) Graphical abstract. IL‐6 induced VSMC phenotypic switch though JAK/STAT. L–O) Western blot analysis and quantification of p‐JAK/JAK, p‐STAT/STAT, SM22α, and α‐SMA expressed in VSMCs ( n = 3 per group). * p < 0.05, ** p < 0.01 and *** p < 0.001. Data were presented as the mean ± SD and analyzed by using one‐way ANOVA, Tukey's multiple comparisons test.

Article Snippet: The membranes were blocked with 5% non‐fat milk in TBST for 1 h at room‐temperature and then incubated overnight at 4 °C with the following primary antibodies: NOX1 (Proteintech, 17772‐1‐AP, 1:1000), p‐IκBα (Santa Cruz, sc‐8404, 1:1000), IκBα (Santa Cruz, sc‐1643, 1:1000), IL‐6 (Santa Cruz, sc‐35596, 1:1000), p‐JAK (Abclonal, AP0531, 1:1000), JAK (Santa Cruz, sc‐390539, 1:1000), p‐STAT (CST, 9145S, 1:1000), STAT (CST, 9139S, 1:1000), Collagen I (Abclonal, A16891, 1:1000), α‐SMA (CST, 48938S, 1:1000), SM22α (Santa Cruz, sc‐53932, 1:1000), α‐Tubulin (CST, 2144S, 1:1000), and GAPDH (CST, 2118S, 1:1000).

Techniques: Control, Quantitative Proteomics, Expressing, Western Blot