Systemic immune changes have been implicated in amyotrophic lateral sclerosis (ALS), but precise mechanisms and cellular targets remain unknown. Neuromuscular junction (NMJ) denervation is another major pathophysiological event in ALS, but it remains unclear whether immune system dysregulation contributes to this process. Here, we report leukocyte and macrophage infiltration in ALS patient-derived skeletal muscle biopsies. Immune cell infiltration was replicated across the hTDP-43, TDP-43(A315T) (male only) and TDP-43(M337V) mouse models, occurring from pre-symptomatic stages and targeted to NMJ-enriched muscle regions. Proteomic analysis implicated the CCL2-CCR2 axis as a driving factor. CCL2(+) cells were enriched around NMJs in hTDP-43 mice, and in ALS patient skeletal muscle. Local treatment with CCL2-neutralising antibodies or normal IgG antibodies in hTDP-43 mice reduced leukocyte infiltration and ameliorated NMJ denervation. These results demonstrate that the CCL2-CCR2 axis drives immune cell infiltration targeting NMJs in ALS, identifying a potential avenue for therapeutic intervention to prevent NMJ denervation.
The CCL2-CCR2 axis drives neuromuscular denervation in amyotrophic lateral sclerosis.
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作者:Nógrádi Bernát, Molnár Kinga, Kristóf Rebeka, Horváth Orsolya, Huang Yu-Ting, Ridgway Zara, Elicegui Amaia, Fuertes-Alvarez Sandra, Alonso-Martin Sonia, Szebeni Gábor J, Gémes Nikolett, Ramadan Abdullah, Smith Hannah L, Krizbai István A, Patai Roland, Siklós László, Klivényi Péter, Chaytow Helena, Gillingwater Thomas H
期刊: | Nature Communications | 影响因子: | 15.700 |
时间: | 2025 | 起止号: | 2025 Aug 1; 16(1):7053 |
doi: | 10.1038/s41467-025-62351-3 |
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