,

Guofang Xia1, Simeng Zhu1, Yujia Liu2

  • 1Department of Cardiology, Shanghai Jiao Tong University School of Medicine Affiliated Sixth People's Hospital, Shanghai, China.

概括

衰老显著改变心脏寄居巨细胞 (CRMs),增加CCR2+和CCR2-子集中的炎症基因表达. 这项研究揭示了CRM功能随着年龄的增长而发生的关键变化,影响心脏健康.

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