Macrophage polarization and diabetic wound healing
- PMID: 34089902
- DOI: 10.1016/j.trsl.2021.05.006
Macrophage polarization and diabetic wound healing
Abstract
Diabetes mellitus is a costly disease and nearly one-third of these costs are attributed to management of diabetic foot disease including chronic, non-healing, diabetic foot ulcers. Therefore, much effort has been placed into understanding the pathogenesis of diabetic wounds and novel therapeutics. A relatively new area of interest has been macrophage polarization and its role in diabetic wound healing. Diabetic wounds show dysregulated and persistent M1 (pro-inflammatory) macrophage polarization whereas normal wounds will display a transition to M2 (pro-healing) macrophages around day three after wounding. We reviewed factors known to affect macrophage polarization, mostly focused on those that contribute to M2 macrophage polarization, and potential treatments that at least in part target macrophage polarization in the diabetic wound bed. Much of the work has been aimed at reducing hyperglycemia and encouraging pro-inflammatory cytokine neutralization or decreased expression given this has a significant role in producing M1 macrophages. Treatment of diabetic wounds will likely require a multi-modal approach including management of underlying diabetes and control of hyperglycemia, topical therapeutics, and prevention of secondary infection and inflammation.
Published by Elsevier Inc.
Similar articles
-
Role of microRNA-21 and Its Underlying Mechanisms in Inflammatory Responses in Diabetic Wounds.Int J Mol Sci. 2020 May 8;21(9):3328. doi: 10.3390/ijms21093328. Int J Mol Sci. 2020. PMID: 32397166 Free PMC article.
-
Uncovering Sex-Related Differences in Skin Macrophage Polarization During Wound Healing in Diabetic Mice.Front Biosci (Landmark Ed). 2025 Feb 17;30(2):27113. doi: 10.31083/FBL27113. Front Biosci (Landmark Ed). 2025. PMID: 40018936
-
Long Noncoding RNA GAS5 Regulates Macrophage Polarization and Diabetic Wound Healing.J Invest Dermatol. 2020 Aug;140(8):1629-1638. doi: 10.1016/j.jid.2019.12.030. Epub 2020 Jan 28. J Invest Dermatol. 2020. PMID: 32004569 Free PMC article.
-
The physiological phenomenon and regulation of macrophage polarization in diabetic wound.Mol Biol Rep. 2023 Nov;50(11):9469-9477. doi: 10.1007/s11033-023-08782-x. Epub 2023 Sep 9. Mol Biol Rep. 2023. PMID: 37688679 Review.
-
Skin Wound Healing: Normal Macrophage Function and Macrophage Dysfunction in Diabetic Wounds.Molecules. 2021 Aug 13;26(16):4917. doi: 10.3390/molecules26164917. Molecules. 2021. PMID: 34443506 Free PMC article. Review.
Cited by
-
Neddylation suppression by a macrophage membrane-coated nanoparticle promotes dual immunomodulatory repair of diabetic wounds.Bioact Mater. 2024 Jan 6;34:366-380. doi: 10.1016/j.bioactmat.2023.12.025. eCollection 2024 Apr. Bioact Mater. 2024. PMID: 38269308 Free PMC article.
-
N6-methyladenosine in myeloid cells: a novel regulatory factor for inflammation-related diseases.J Physiol Biochem. 2024 May;80(2):249-260. doi: 10.1007/s13105-023-01002-x. Epub 2023 Dec 30. J Physiol Biochem. 2024. PMID: 38158555 Review.
-
Turning sublimed sulfur and bFGF into a nanocomposite to accelerate wound healing via co-activate FGFR and Hippo signaling pathway.Mater Today Bio. 2024 May 27;26:101104. doi: 10.1016/j.mtbio.2024.101104. eCollection 2024 Jun. Mater Today Bio. 2024. PMID: 38952539 Free PMC article.
-
Progress and expectation of stem cell therapy for diabetic wound healing.World J Clin Cases. 2023 Jan 26;11(3):506-513. doi: 10.12998/wjcc.v11.i3.506. World J Clin Cases. 2023. PMID: 36793646 Free PMC article. Review.
-
Human Keratinocyte-Derived Exosomal MALAT1 Promotes Diabetic Wound Healing by Upregulating MFGE8 via microRNA-1914-3p.Int J Nanomedicine. 2023 Feb 21;18:949-970. doi: 10.2147/IJN.S399785. eCollection 2023. Int J Nanomedicine. 2023. PMID: 36852184 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical