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. Author manuscript; available in PMC: 2016 Jan 28.
Published in final edited form as: Calcif Tissue Int. 2015 Feb 25;96(5):465–475. doi: 10.1007/s00223-015-9967-7

Fig. 3.

Fig. 3

Reduction of LNX2 expression in macrophages inhibits M-CSF and RANKL signaling pathways. Lentivirus-transduced BMMs were serum-starved overnight and were then stimulated with 50ng/ml M-CSF (A) and 100ng/ml RANKL (B) for the indicated times. The activation of downstream signaling pathways was detected by western blots using specific antibodies. Total ERK and AKT in (A) and Actin and total JNK in (B) served as loading controls. The representative data from three experiments were presented.