4.6 Article

Enhanced Proliferation of Ly6C+ Monocytes/Macrophages Contributes to Chronic Inflammation in Skin Wounds of Diabetic Mice

Journal

JOURNAL OF IMMUNOLOGY
Volume 206, Issue 3, Pages 621-+

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.2000935

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Funding

  1. National Institute of General Medical Sciences [R01GM092850, R35GM136228]
  2. National Center for Advancing Translational Sciences [UL1TR002003]

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Diabetic wounds exhibit higher proliferation rates of Ly6C(+)F4/8(lo/-) Mo/M Phi, contributing to their greater accumulation in the wounds compared to nondiabetic mice. CCL2/CCR2 signaling pathway promotes skin Mo/M Phi proliferation in diabetic mice, which leads to impaired healing.
Diabetic wounds are characterized by persistent accumulation of proinflammatory monocytes (Mo)/macrophages (M Phi) and impaired healing. However, the mechanisms underlying the persistent accumulation of Mo/Me remain poorly understood. In this study, we report that Ly6C(+)F4/8(lo/-) Mo/M Phi proliferate at higher rates in wounds of diabetic mice compared with nondiabetic mice, leading to greater accumulation of these cells. Unbiased single cell RNA sequencing analysis of combined nondiabetic and diabetic wound Mo/M Phi revealed a cluster, populated primarily by cells from diabetic wounds, for which genes associated with the cell cycle were enriched. In a screen of potential regulators, CCL2 levels were increased in wounds of diabetic mice, and subsequent experiments showed that local CCL2 treatment increased Ly6C(+)F4/80(lo/-) Mo/Me proliferation. Importantly, adoptive transfer of mixtures of CCR2(-/- )and CCR2(+/+ )Ly6C(hi) Mo indicated that CCL2/CCR2 signaling is required for their proliferation in the wound environment. Together, these data demonstrate a novel role for the CCL2/CCR2 signaling pathway in promoting skin Mo/M Phi proliferation, contributing to persistent accumulation of Mo/Me and impaired healing in diabetic mice.

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