Pak4-mediated crosstalk between necroptotic macrophages and tendon stem/progenitor cells contributes to traumatic heterotopic ossification formation

The formation of traumatic heterotopic ossification (HO) is an abnormal repair process after soft tissue injury. Recent studies establish the involvement of immune cells and cellular metabolism in the tissue healing process; however, their role in HO remains unknown. Here, by using murine burn/tenotomy model in vivo and tendon stem/progenitor cells (TSPCs) osteogenic differentiation model in vitro, together with techniques including transgenic knockout, gene knockdown, transcriptome and proteome sequencings, mass spectrometry, co-immunoprecipitation, seahorse, etc., we reveal a novel p21-activated kinase 4 (Pak4) mediated crosstalk where the necroptotic macrophages arouse TSPCs with reduced fatty acid β-oxidation (FAO), to promote aberrant osteogenic differentiation during HO formation. Necroptosis blockade with Mlkl knockout (C57BL/6JGpt-Mlkl<sup>em1Cd1679</sup>/Gpt) significantly reduces HO than WT mice. Extracellular vesicle (EVs) secreted from necroptotic bone marrow-derived macrophages (BMDMs, NecroMφ-EVs) are determined to motivate FAO reduction in TSPCs and result in higher osteogenic activity. Pak4 conditional knockout (C57BL/6JGpt-Pak4<sup>em1Cflox</sup>/Gpt) in macrophage significantly increases FAO and reduces HO than Flox mice, as well as local injection of PAK4<sup>-/-</sup>-EVs (NecroMφ-EVs with Pak4 knockout) than NecroMφ-EVs, and the protective effects are reversed after transfection of Fabp3<sup>S122D</sup>, a phosphomimetic mutant of S122 on fatty acid binding protein 3 (Fabp3) phosphorylation site. Mechanically, after soft tissue injury, macrophages infiltrate, and necroptosis occurs, accompanied by paracrine EVs-derived Pak4, which binds directly to Fabp3 and phosphorylates it at the S122 site in TSPCs, results in reduced FAO, finally osteogenic behavior, and HO formation. This study adds perceptiveness into abnormal regeneration-based theory for traumatic HO and raises treatment strategy development.

Authors

Institutions

Publication Details

Journal
Bone Research
Published
2025-10-20
DOI
https://doi.org/10.1038/s41413-025-00463-8
Primary Topic
Heterotopic Ossification and Related Conditions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Pak4-mediated crosstalk between necroptotic macrophages and tendon stem/progenitor cells contributes to traumatic heterotopic ossification formation

Ziyang Sun, Cunyi Fan, Kuangyu He, Juehong Li et al.
Bone Research
Heterotopic Ossification and Related Conditions
article

Pak4-mediated crosstalk between necroptotic macrophages and tendon stem/progenitor cells contributes to traumatic heterotopic ossification formation

Ziyang Sun, Cunyi Fan, Kuangyu He, Juehong Li, Gang Luo, Hang Liu, Zhengqiang Yuan, Hongjiang Ruan, Yi Xu, Zhenyu Chen, Qian Chen
article en

Abstract

The formation of traumatic heterotopic ossification (HO) is an abnormal repair process after soft tissue injury. Recent studies establish the involvement of immune cells and cellular metabolism in the tissue healing process; however, their role in HO remains unknown. Here, by using murine burn/tenotomy model in vivo and tendon stem/progenitor cells (TSPCs) osteogenic differentiation model in vitro, together with techniques including transgenic knockout, gene knockdown, transcriptome and proteome sequencings, mass spectrometry, co-immunoprecipitation, seahorse, etc., we reveal a novel p21-activated kinase 4 (Pak4) mediated crosstalk where the necroptotic macrophages arouse TSPCs with reduced fatty acid β-oxidation (FAO), to promote aberrant osteogenic differentiation during HO formation. Necroptosis blockade with Mlkl knockout (C57BL/6JGpt-Mlkl<sup>em1Cd1679</sup>/Gpt) significantly reduces HO than WT mice. Extracellular vesicle (EVs) secreted from necroptotic bone marrow-derived macrophages (BMDMs, NecroMφ-EVs) are determined to motivate FAO reduction in TSPCs and result in higher osteogenic activity. Pak4 conditional knockout (C57BL/6JGpt-Pak4<sup>em1Cflox</sup>/Gpt) in macrophage significantly increases FAO and reduces HO than Flox mice, as well as local injection of PAK4<sup>-/-</sup>-EVs (NecroMφ-EVs with Pak4 knockout) than NecroMφ-EVs, and the protective effects are reversed after transfection of Fabp3<sup>S122D</sup>, a phosphomimetic mutant of S122 on fatty acid binding protein 3 (Fabp3) phosphorylation site. Mechanically, after soft tissue injury, macrophages infiltrate, and necroptosis occurs, accompanied by paracrine EVs-derived Pak4, which binds directly to Fabp3 and phosphorylates it at the S122 site in TSPCs, results in reduced FAO, finally osteogenic behavior, and HO formation. This study adds perceptiveness into abnormal regeneration-based theory for traumatic HO and raises treatment strategy development.

Bone ResearchVol. 13(1)
Shanghai Innovative Research Center of Traditional Chinese Medicine (CN), Shanghai Sixth People's Hospital (CN)
Openalex Percentile: Top 57%
Heterotopic Ossification and Related Conditions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.