Mast Cells in Diabetes and Diabetic Wound Healing

被引:71
作者
Dong, Jie [1 ,2 ]
Chen, Lihong [1 ,2 ]
Zhang, Ying [1 ,2 ]
Jayaswal, Navin [1 ,2 ]
Mezghani, Ikram [1 ,2 ]
Zhang, Weijie [1 ,2 ,3 ]
Veves, Aristidis [1 ,2 ]
机构
[1] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Joslin Beth Israel Deaconess Foot Ctr, Boston, MA 02115 USA
[2] Care of Xu RX, Harvard Med Sch, Ctr Regenerat Therapeut, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[3] LanZhou Univ Technol, 287 Langongping Rd, Lanzhou, Gansu, Peoples R China
基金
美国国家卫生研究院;
关键词
Diabetes mellitus; Diabetic foot ulcer; Mast cells; Wound healing; MEDIATOR RELEASE; PROTECTS MICE; OBESITY; INFLAMMATION; PROLIFERATION; DEFICIENCY; DENSITY; CHYMASE; PATHOGENESIS; MACROPHAGES;
D O I
10.1007/s12325-020-01499-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mast cells (MCs) are granulated, immune cells of the myeloid lineage that are present in connective tissues. Apart from their classical role in allergies, MCs also mediate various inflammatory responses due to the nature of their secretory products. They are involved in important physiological and pathophysiological responses related to inflammation, chronic wounds, and autoimmune diseases. There are also indications that MCs are associated with diabetes and its complications. MCs and MC-derived mediators participate in all wound healing stages and are involved in the pathogenesis of non-healing, chronic diabetic foot ulcers (DFUs). More specifically, recent work has shown increased degranulation of skin MCs in human diabetes and diabetic mice, which is associated with impaired wound healing. Furthermore, MC stabilization, either systemic or local at the skin level, improves wound healing in diabetic mice. Understanding the precise role of MCs in wound progression and healing processes can be of critical importance as it can lead to the development of new targeted therapies for diabetic foot ulceration, one of the most devastating complications of diabetes.
引用
收藏
页码:4519 / 4537
页数:19
相关论文
共 99 条
[1]   Mast cell-orchestrated immunity to pathogens [J].
Abraham, Soman N. ;
St John, Ashley L. .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (06) :440-452
[2]   Leptin deficiency-induced obesity affects the density of mast cells in abdominal fat depots and lymph nodes in mice [J].
Altintas, Mehmet M. ;
Nayer, Behzad ;
Walford, Eric C. ;
Johnson, Kevin B. ;
Gaidosh, Gabriel ;
Reiser, Jochen ;
De La Cruz-Munoz, Nestor ;
Ortega, Luis M. ;
Nayer, Ali .
LIPIDS IN HEALTH AND DISEASE, 2012, 11
[3]   Mast Cells Are Dispensable for Normal and Activin-Promoted Wound Healing and Skin Carcinogenesis [J].
Antsiferova, Maria ;
Martin, Caroline ;
Huber, Marcel ;
Feyerabend, Thorsten B. ;
Foerster, Anja ;
Hartmann, Karin ;
Rodewald, Hans-Reimer ;
Hohl, Daniel ;
Werner, Sabine .
JOURNAL OF IMMUNOLOGY, 2013, 191 (12) :6147-6155
[4]   Effect of Omegaven on mast cell concentration in diabetic wound healing [J].
Babaei, Saeid ;
Ansarihadipour, Hadi ;
Nakhaei, Mahmoodreza ;
Darabi, Mohammadreza ;
Bayat, Parvindokht ;
Sakhaei, Mohammadhassan ;
Baazm, Maryam ;
Mohammadhoseiny, Atefe .
JOURNAL OF TISSUE VIABILITY, 2017, 26 (02) :125-130
[5]   The mast cell demystified: A novel target for anti-inflammatory strategies after circulatory arrest? [J].
Balsam, Leora B. ;
DeAnda, Abe, Jr. .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2017, 153 (01) :77-78
[6]   Our perception of the mast cell from Paul Ehrlich to now [J].
Beaven, Michael A. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2009, 39 (01) :11-25
[7]   Mast cells contribute to autoimmune diabetes by releasing interleukin-6 and failing to acquire a tolerogenic IL-10+ phenotype [J].
Betto, Elena ;
Usuelli, Vera ;
Mandelli, Alessandra ;
Badami, Ester ;
Sorini, Chiara ;
Capolla, Sara ;
Danelli, Luca ;
Frossi, Barbara ;
Guarnotta, Carla ;
Ingrao, Sabrina ;
Tripodo, Claudio ;
Pucillo, Carlo ;
Gri, Giorgia ;
Falcone, Marika .
CLINICAL IMMUNOLOGY, 2017, 178 :29-38
[8]   IL-4 enhances proliferation and mediator release in mature human mast cells [J].
Bischoff, SC ;
Sellge, G ;
Lorentz, A ;
Sebald, W ;
Raab, R ;
Manns, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (14) :8080-8085
[9]   Genetics, pathogenesis and clinical interventions in type 1 diabetes [J].
Bluestone, Jeffrey A. ;
Herold, Kevan ;
Eisenbarth, George .
NATURE, 2010, 464 (7293) :1293-1300
[10]  
Bot I, 2020, CELLS, V2020, P9