Lactate induces osteoblast differentiation by stabilization of HIF1α

- Lactate induces osteoblast differentiation in in vitro cellular model.
- MCT1 and LDHB are pivotal for osteoblast differentiation that induced by lactate.
- Lactate stabilizes HIF1α by inhibiting its ubiquitin dependent protein degradation.
- Inhibited HIF1α activity impairs osteoblast differentiation that induced by lactate.

Aerobic glycolysis is involved in osteoblast differentiation induced by Wnt signaling or PTH treatment. However, it is still unclear whether lactate, the end product of aerobic glycolysis, plays any role in osteoblast differentiation. Herein we report that in cultures of osteoblast-lineage cells, lactate promoted alkaline phosphatase-positive cell formation, increased the activity of alkaline phosphatase, and induced the expression of osteocalcin. This osteoblast differentiation-inducing effect of lactate can be inhibited by blocking its entry into cells with MCT1 siRNA or inhibitors, and by interfering with its metabolism by using specific siRNAs for LDHB and PDH. Moreover, lactate stabilized HIF1α expression and inhibited HIF1α activity, with BAY87-2243 lowering the osteoblast differentiation-inducing effect of lactate. Thus, these findings reveal an unrecognized role for aerobic glycolysis in osteoblast differentiation via its end product, lactate.

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