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. Author manuscript; available in PMC: 2015 Apr 1.

Published in final edited form as: Atherosclerosis. 2014 Jan 21;233(2):419–428. doi: 10.1016/j.atherosclerosis.2014.01.011

(A) Representative histograms and flow cytometry result summary showing the homing of T_H1 cells into spleen, PGAT, and skeletal muscle of HFD-fed TCRb−/− mice after adoptive transfer (n=3–4 mice/group). (B) Inflammatory gene expression in PGAT and skeletal muscle of HFD-fed TCRb−/− mice injected with PBS or T_H1 cells (n=5 mice/group). (C) Fasting glucose and (D) insulin tolerance test in HFD-fed TCRb−/− mice after 12 weeks of adoptive T_H1 cell transfer (n=8 mice/group). Panels A and B are shown as mean±SEM; panels C and D are shown as mean±SD of 2 separate experiments. *P<0.05, **P<0.01, ***P<0.001.

(A) Representative histograms and flow cytometry result summary showing the homing of T_H1 cells into spleen, PGAT, and skeletal muscle of HFD-fed TCRb−/− mice after adoptive transfer (n=3–4 mice/group). (B) Inflammatory gene expression in PGAT and skeletal muscle of HFD-fed TCRb−/− mice injected with PBS or T_H1 cells (n=5 mice/group). (C) Fasting glucose and (D) insulin tolerance test in HFD-fed TCRb−/− mice after 12 weeks of adoptive T_H1 cell transfer (n=8 mice/group). Panels A and B are shown as mean±SEM; panels C and D are shown as mean±SD of 2 separate experiments. *P<0.05, **P<0.01, ***P<0.001.