Earlier onset of chemotherapy-induced neuropathic pain in females by ICAM-1–mediated accumulation of perivascular macrophages

IF 11.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Li Chen, Xin Zou, Cui-Cui Liu, Pu Yan, Jie Deng, Chen Wang, Mu-Yang Chen, Xiao-Qing Tang, Jing-Ming Shi, Wen-Jun Xin, Xiang-Zhong Zhang, Xia Feng, Ting Xu, Jing-Dun Xie
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Abstract

Sex differences in the pathogenesis of a variety of diseases have drawn increasing attention. However, it remains unclear whether such differences exist in chemotherapy-induced neuropathic pain. Here, we conducted a retrospective analysis of clinical case data and found that peripheral sensory disorders occurred earlier in females than in males following bortezomib (BTZ) treatment in patients with multiple myeloma. BTZ treatment led to an early elevation of intercellular adhesion molecule–1, which triggered the infiltration of peripheral monocytes into the perivascular region of the spinal cord in female mice. The CC-chemokine ligand 1 released by infiltrating macrophages directly activated neurons or indirectly activated neurons by enhancing the astrocyte activity, ultimately leading to the earlier onset of BTZ-induced neuropathic pain in females. Together, clarifying the mechanism underlying the earlier onset of BTZ-induced neuropathic pain will contribute to the precise treatment of multiple myeloma in females.

Abstract Image

由icam -1介导的血管周围巨噬细胞积累引起的化疗诱导的女性神经性疼痛的早期发病
性别差异在多种疾病发病机制中的作用日益引起人们的重视。然而,尚不清楚这种差异是否存在于化疗引起的神经性疼痛中。在这里,我们对临床病例数据进行了回顾性分析,发现在多发性骨髓瘤患者接受硼替佐米(BTZ)治疗后,女性比男性更早出现外周感觉障碍。BTZ处理导致雌性小鼠细胞间粘附分子- 1的早期升高,从而引发外周单核细胞向脊髓血管周围区浸润。浸润巨噬细胞释放的cc趋化因子配体1通过增强星形胶质细胞活性直接激活神经元或间接激活神经元,最终导致btz诱导的雌性神经性疼痛发病提前。总之,阐明btz诱发的神经性疼痛早期发病的机制将有助于女性多发性骨髓瘤的精确治疗。
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来源期刊
Science Advances
Science Advances 综合性期刊-综合性期刊
CiteScore
21.40
自引率
1.50%
发文量
1937
审稿时长
29 weeks
期刊介绍: Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.
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