Journal: Biochemical and biophysical research communications
Article Title: Growth hormone resistance induced by amino acid deprivation in fao cells is independent of FGF21.
doi: 10.1016/j.bbrc.2024.149811
Figure Lengend Snippet: Fig. 3. Effect of FGH21 addition on GH signaling. A, B) Immunoblotting of JAK2, p-JAK2, STAT5b, and HSP90. Fao cells were cultured in the Full or Zero medium with 0–10 [5] pM of recombinant FGF21 for 24 h. Cells were then treated with 100 nM GH or vehicle for 10 min. C) Igf1 mRNA levels were quantified using real-time qPCR. Values were normalized against the Actb mRNA level. Fao cells were cultured in the full medium with or without 100 nM GH and 0–105 pM of FGF21 for 24 h. Total RNA was isolated. Bar: means ± SEM (n = 3), *p < 0.05. (D) The expression of α-klotho (Kl), β-klotho (Klb), and FGF Receptor (Fgfr) 1–4 in Fao cells, rat primary hepatocytes, and rat tissue samples were analyzed using reverse transcription-PCR. (E) Immnoblotting of Erk and p-Erk. Fao cells were cultured in the full medium for 24 h. The cells were then treated with 0–104 pM of FGF21 or vehicle for 10 min.
Article Snippet: Plasma FGF21 concentrations were measured using a mouse/rat FGF21 ELISA kit (Proteintech, IL, USA).
Techniques: Western Blot, Cell Culture, Recombinant, Isolation, Expressing, Reverse Transcription