Evidence map›Paper›PMID 42835090›Full record

ArticleFrontiers in physiology2026

Pannexin 3-mediated adenosine triphosphate release from pre-osteoblasts promotes osteoblast differentiation through P2X4 receptor activation.

Hiroaki Kito, Ayano Niwa, Takusei Ryu, Yohei Yamaguchi, Junko Kajikuri, Susumu Ohya

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Article in Frontiers in physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hiroaki KitoDepartment of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
Ayano NiwaDepartment of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
Takusei RyuDepartment of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
Yohei YamaguchiDepartment of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
Junko KajikuriDepartment of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
Susumu OhyaDepartment of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased pre-osteoblast cell density within bone resorption areas is a key factor in promoting osteoblast differentiation; however, the molecular mechanisms underlying this process remain poorly understood. In this study, we investigated the role of ATP release and purinergic receptor P2X4 signaling in osteoblast differentiation using the murine pre-osteoblastic cell line MC3T3-E1. Under high cell density conditions, which were essential for the induction of osteoblast differentiation, we observed a significant accumulation of extracellular ATP released via the hemichannel Pannexin 3 (Panx3). This ATP accumulation subsequently activated the P2X4. Pharmacological inhibition and siRNA-mediated knockdown Panx3 markedly reduced extracellular ATP levels and decreased expression and activity of alkaline phosphatase (ALP), an osteoblast differentiation marker. Similarly, pharmacological inhibition and siRNA-mediated knockdown of P2X4 suppressed ALP expression and activity. Functional analyses using calcium imaging and whole-cell patch-clamp recording revealed that P2X4 activity was enhanced during osteoblast differentiation. Notably, this functional upregulation correlated with enhanced localization of P2X4 to the plasma membrane. Moreover, pharmacological inhibition of Panx3 or P2X4 impaired the endochondral ossification of isolated mouse metatarsal bone. These findings suggest that Panx3-mediated ATP release and the subsequent activation of P2X4 signaling constitute a crucial pathway linking cell density to osteoblast differentiation. Our study provides new insights into the purinergic signaling mechanisms underlying bone formation and identifies potential molecular targets for promoting osteogenesis.

Indexed as

ATPdifferentiationosteoblastP2X4Pannexin 3

Identifiers

PMID42835090
PMCPMC13634857

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