Macrophages as a therapeutic target to promote diabetic wound healing

被引:275
作者
Sharifiaghdam, Maryam [1 ,2 ]
Shaabani, Elnaz [1 ,2 ]
Faridi-Majidi, Reza [2 ]
De Smedt, Stefaan C. [1 ]
Braeckmans, Kevin [1 ,3 ]
Fraire, Juan C. [1 ]
机构
[1] Univ Ghent, Fac Pharm, Lab Gen Biochem & Phys Pharm, B-9000 Ghent, Belgium
[2] Univ Tehran Med Sci, Sch Adv Technol Med, Dept Med Nanotechnol, Tehran, Iran
[3] Univ Ghent, Ctr Adv Light Microscopy, B-9000 Ghent, Belgium
关键词
NECROSIS-FACTOR-ALPHA; STIMULATING FACTOR-I; M2; MACROPHAGES; TISSUE-REPAIR; HUMAN MONOCYTES; GENE-THERAPY; TNF-ALPHA; CELLS; SIRNA; ACTIVATION;
D O I
10.1016/j.ymthe.2022.07.016
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
It is well established that macrophages are key regulators of wound healing, displaying impressive plasticity and an evolving phenotype, from an aggressive pro-inflammatory or "M1" phenotype to a pro-healing or "M2" phenotype, depending on the wound healing stage, to ensure proper healing. Because dysregulated macrophage responses have been linked to impaired healing of diabetic wounds, macrophages are being considered as a therapeutic target for improved wound healing. In this review, we first discuss the role of macrophages in a normal skin wound healing process and discuss the aberrations that occur in macrophages under diabetic conditions. Next we provide an overview of recent macrophage-based therapeutic approaches, including delivery of ex-vivo-activated macrophages and delivery of pharmacological strategies aimed at eliminating or re-educating local skin macrophages. In particular, we focus on strategies to silence key regulator genes to repolarize wound macrophages to the M2 phenotype, and we provide a discussion of their potential future clinical translation.
引用
收藏
页码:2891 / 2908
页数:18
相关论文
共 168 条
[1]   Activation of PPAR-γ induces macrophage polarization and reduces neutrophil migration mediated by heme oxygenase 1 [J].
Abdalla, Henrique Ballassini ;
Napimoga, Marcelo Henrique ;
Lopes, Alexandre Hashimoto ;
de Macedo Maganin, Alexandre Gomes ;
Cunha, Thiago Mattar ;
Van Dyke, Thomas E. ;
Clemente Napimoga, Juliana Trindade .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2020, 84
[2]   Skin Wound Healing: Normal Macrophage Function and Macrophage Dysfunction in Diabetic Wounds [J].
Aitcheson, Savannah M. ;
Frentiu, Francesca D. ;
Hurn, Sheree E. ;
Edwards, Katie ;
Murray, Rachael Z. .
MOLECULES, 2021, 26 (16)
[3]   Repetitive Intermittent Hyperglycemia Drives the M1 Polarization and Inflammatory Responses in THP-1 Macrophages Through the Mechanism Involving the TLR4-IRF5 Pathway [J].
Al-Rashed, Fatema ;
Sindhu, Sardar ;
Arefanian, Hossein ;
Al Madhoun, Ashraf ;
Kochumon, Shihab ;
Thomas, Reeby ;
Al-Kandari, Sarah ;
Alghaith, Abdulwahab ;
Jacob, Texy ;
Al-Mulla, Fahd ;
Ahmad, Rasheed .
CELLS, 2020, 9 (08)
[4]   Myelin damage and repair in pathologic CNS: challenges and prospects [J].
Alizadeh, Arsalan ;
Dyck, Scott M. ;
Karimi-Abdolrezaee, Soheila .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2015, 8
[5]   Advances and challenges in targeting IRF5, a key regulator of inflammation [J].
Almuttaqi, Hannah ;
Udalova, Irina A. .
FEBS JOURNAL, 2019, 286 (09) :1624-1637
[6]   Molecular Mechanisms Modulating the Phenotype of Macrophages and Microglia [J].
Amici, Stephanie A. ;
Dong, Joycelyn ;
Guerau-de-Arellano, Mireia .
FRONTIERS IN IMMUNOLOGY, 2017, 8
[7]   Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis [J].
Arnold, Ludovic ;
Henry, Adeline ;
Poron, Francoise ;
Baba-Amer, Yasmine ;
van Rooijen, Nico ;
Plonquet, Anne ;
Gherardi, Romain K. ;
Chazaud, Benedicte .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (05) :1057-1069
[8]   Tumor necrosis factor-alpha (TNF-a) is a therapeutic target for impaired cutaneous wound healing [J].
Ashcroft, Gillian S. ;
Jeong, Moon-Jin ;
Ashworth, Jason J. ;
Hardman, Matthew ;
Jin, Wenwen ;
Moutsopoulos, Niki ;
Wild, Teresa ;
McCartney-Francis, Nancy ;
Sim, Davis ;
McGrady, George ;
Song, Xiao-yu ;
Wahl, Sharon M. .
WOUND REPAIR AND REGENERATION, 2012, 20 (01) :38-49
[9]   Diabetes induces myeloid bias in bone marrow progenitors associated with enhanced wound macrophage accumulation and impaired healing [J].
Barman, Pijus K. ;
Urao, Norifumi ;
Koh, Timothy J. .
JOURNAL OF PATHOLOGY, 2019, 249 (04) :435-446
[10]   Skin Wounding-Induced Monocyte Expansion in Mice Is Not Abrogated by IL-1 Receptor 1 Deficiency [J].
Barman, Pijus K. ;
Pang, Jingbo ;
Urao, Norifumi ;
Koh, Timothy J. .
JOURNAL OF IMMUNOLOGY, 2019, 202 (09) :2720-2727