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巨噬细胞清除可恢复背根神经节微环境并预防硼替佐米诱导的神经病变中的轴突退化。

Macrophage depletion restores the DRG microenvironment and prevents axon degeneration in bortezomib-induced neuropathy.

作者信息

Thomsen Michael B, Singh Abhishek, Thebeau Christina N, Gao Vivian D, Schulze Nicholas F, Avraham Oshri, Yang Sarah X, Koneru Shriya, Geier Sami S, Landon Shannon M, Pelea Aidan, Cavalli Valeria, Geisler Stefanie

机构信息

CS27 Bioinformatics; Springboro, USA.

Department of Neurology, Washington University School of Medicine in St. Louis; St. Louis, USA.

出版信息

bioRxiv. 2025 Jan 24:2025.01.22.634362. doi: 10.1101/2025.01.22.634362.

Abstract

Peripheral neuropathy is a common and debilitating side effect of the chemotherapeutic bortezomib (BTZ). To explore the mechanisms underlying BTZ-induced neuropathy (BIPN), we developed a mouse model that replicates the route of administration and approximates the prolonged BTZ exposure experienced by patients. We find that male mice treated with BTZ experience more severe sensorimotor dysfunction and axon loss compared to females and observed similar results when analyzing human data. Using single cell RNA-sequencing, we reveal that BTZ significantly alters the dorsal root ganglia (DRG) microenvironment in mice, producing pronounced sex-specific changes in satellite glial cells (SGCs) in males and females and dysregulation of the extracellular matrix (ECM), particularly in males. These changes are accompanied by expansion of macrophages, which is more pronounced in males. We identify four macrophage subtypes in the DRG, including a pro-fibrotic population that is exclusively associated with BIPN. Depletion of macrophages via anti-CSF1R treatment in male mice prevents BTZ-induced SGC activation and aberrant collagen deposition in DRGs, potently preserves peripheral axons, and improves functional outcomes. These findings highlight SGCs, neuroinflammation and dysregulation of the ECM as drivers of sex-specific differences in BIPN and suggest that targeting neuroinflammation is a promising therapeutic strategy to treat this disease.

摘要

周围神经病变是化疗药物硼替佐米(BTZ)常见且使人衰弱的副作用。为探究BTZ诱导的神经病变(BIPN)的潜在机制,我们建立了一种小鼠模型,该模型复制了给药途径并模拟了患者经历的BTZ长期暴露情况。我们发现,与雌性小鼠相比,接受BTZ治疗的雄性小鼠出现更严重的感觉运动功能障碍和轴突损失,并且在分析人类数据时也观察到了类似结果。通过单细胞RNA测序,我们揭示BTZ显著改变了小鼠背根神经节(DRG)的微环境,在雄性和雌性小鼠的卫星神经胶质细胞(SGC)中产生了明显的性别特异性变化,以及细胞外基质(ECM)失调,在雄性小鼠中尤为明显。这些变化伴随着巨噬细胞的扩增,在雄性小鼠中更为显著。我们在DRG中鉴定出四种巨噬细胞亚型,包括一种仅与BIPN相关的促纤维化群体。通过抗CSF1R治疗使雄性小鼠的巨噬细胞耗竭可防止BTZ诱导的SGC激活和DRG中异常胶原沉积,有效保留外周轴突并改善功能结果。这些发现突出了SGC、神经炎症和ECM失调是BIPN中性别特异性差异的驱动因素,并表明靶向神经炎症是治疗这种疾病的一种有前景的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d81/11785175/50027719390f/nihpp-2025.01.22.634362v1-f0001.jpg

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