Toll-like receptor 4 signaling in osteoblasts is required for load-induced bone formation in mice.

Autor:	Rajpar I; Department of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA., Kumar G; Department of Cancer Biology, Thomas Jefferson University, Philadelphia, PA, USA., Fortina P; Department of Cancer Biology, Thomas Jefferson University, Philadelphia, PA, USA., Tomlinson RE; Department of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Jazyk:	angličtina
Zdroj:	IScience [iScience] 2023 Feb 28; Vol. 26 (4), pp. 106304. Date of Electronic Publication: 2023 Feb 28 (Print Publication: 2023).
DOI:	10.1016/j.isci.2023.106304
Abstrakt:	In mature bone, NGF is produced by osteoblasts following mechanical loading and signals through resident sensory nerves expressing its high affinity receptor, neurotrophic tyrosine kinase receptor type 1 (TrkA), to support bone formation. Here, we investigated whether osteoblastic expression of Toll-like receptor 4 (TLR4), a key receptor in the NF-κB signaling pathway, is required to initiate NGF-TrkA signaling required for load-induced bone formation. Although Tlr4 conditional knockout mice have normal skeletal mass and strength in adulthood, the loss of TLR4 signaling significantly reduced lamellar bone formation following loading. Inhibition of TLR4 signaling reduced Ngf expression in primary osteoblasts and RNA sequencing of bones from Tlr4 conditional knockout mice and wild-type littermates revealed dysregulated inflammatory signaling three days after osteogenic mechanical loading. In total, our study reveals an important role for osteoblastic TLR4 in the skeletal adaptation of bone to mechanical forces. Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. (© 2023 The Author(s).)
Databáze:	MEDLINE
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