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Journal: Journal of orthopaedic surgery and research
Article Title: Oncostatin M promotes osteogenic differentiation of tendon-derived stem cells through the JAK2/STAT3 signalling pathway.
doi: 10.1186/s13018-024-04915-5
Figure Lengend Snippet: Fig. 3 Effect of OSM on JAK2/STAT3 signalling pathway during early and middle osteogenic differentiation of tendon stem cells. (A) After OSM-induced osteogenic differentiation of tendon stem cells for 7 days, expression of OSMR, GP130, p-JAK2, and p-STAT3 proteins was detected by western blotting (n = 3). Two-tailed Student’s t-test. (B)Fourteen days after OSM-induced osteogenic differentiation of tendon stem cells, expression of OSMR, GP130, p-JAK2, and p-STAT3 proteins was detected by western blotting (n = 3). Two-tailed Student’s t-test.Data are presented as means ± standard deviation. *p < 0.05; **p < 0.01; ***p < 0.001
Article Snippet: To further analyse the effect of JAK2/STAT3 signalling on osteogenic differentiation of TDSCs,
Techniques: Expressing, Western Blot, Two Tailed Test, Standard Deviation
Journal: Journal of orthopaedic surgery and research
Article Title: Oncostatin M promotes osteogenic differentiation of tendon-derived stem cells through the JAK2/STAT3 signalling pathway.
doi: 10.1186/s13018-024-04915-5
Figure Lengend Snippet: Fig. 4 OSM promotes early and mid-stage osteogenic differentiation of tendon stem cells through the JAK2/STAT3 signalling pathway. (A, B,E)After 7 days of OSM-induced osteogenic differentiation in the presence of AZD1480 and stattic, alkaline phosphatase staining was performed. Scale bar represents 200 μm. Expression of p-JAK2 and p-STAT3 proteins as well as osteogenic marker genes was analysed by western blotting and qPCR(n = 3). One-way ANOVA. (C, D,F) After 14 days of OSM-induced osteogenic differentiation in the presence of AZD1480 and stattic, alizarin red staining was performed. Scale bar represents 200 μm. Expression of p-JAK2 and p-STAT3 proteins and osteogenic marker genes were analysed by western blotting and qPCR, respectively (n = 3). One-way ANOVA. Data are presented as means ± standard deviation. *p < 0.05; **p < 0.01; ***p < 0.001
Article Snippet: To further analyse the effect of JAK2/STAT3 signalling on osteogenic differentiation of TDSCs,
Techniques: Staining, Expressing, Marker, Western Blot, Standard Deviation
Journal: Journal of orthopaedic surgery and research
Article Title: Oncostatin M promotes osteogenic differentiation of tendon-derived stem cells through the JAK2/STAT3 signalling pathway.
doi: 10.1186/s13018-024-04915-5
Figure Lengend Snippet: Fig. 5 OSM promotes osteogenic differentiation of tendon stem cells through the JAK2/STAT3 signalling pathway. OSM binds to the tendon stem cell receptor OSMR/GP130, activating and phosphorylating JAK2. Phosphorylated JAK2 activates STAT3 downstream, and phosphorylated STAT3 forms a dimer that translocates to the nucleus and binds to DNA to regulate gene transcription. AZD1480 and stattic inhibit activation and phosphorylation of JAK2 and STAT3, respectively
Article Snippet: To further analyse the effect of JAK2/STAT3 signalling on osteogenic differentiation of TDSCs,
Techniques: Activation Assay, Phospho-proteomics
Journal: Nutrition & metabolism
Article Title: Spexin ameliorated obesity-related metabolic disorders through promoting white adipose browning mediated by JAK2-STAT3 pathway.
doi: 10.1186/s12986-024-00790-3
Figure Lengend Snippet: Fig. 9 JAK2-STAT3 signaling pathway inhibitors eliminate the adipose browning induced by SPX. The adipocytes were treated with an inhibitor of JAK2 (AZD1480) or an inhibitor of STAT3 (stattic). (A ~ D) The protein expression of UCP1, TBX1 and CIDEA treated with AZD1480 and stattic. (E) The expression levels of mitochondrial biogenesis proteins CYT-B. (F) The mRNA expression of UCP1, TBX1 and CIDEA. All values are represented as means with error bars representing S.D. In the bar graph, *, P < 0.05; **, P < 0.01. n = 6 for each group
Article Snippet: Antibodies UCP1 (ab10983), TBX1 (ab109313) and CIDEA (ab8402) were purchased from Abcam (Cambridge, UK), Actin (AP0063), JAK2 (3230), STAT3 (12,640), p-JAK2 (3771) and p-STAT3 (9145) were from Cell Signaling Technology (Boston, MA, USA), and
Techniques: Expressing