Exosomes derived from mesenchymal stem cells: A promising cell-free therapeutic tool for cutaneous wound healing

被引:17
作者
Zakeri, Armin [1 ]
Khaseb, Sanaz [1 ]
Rahnama, Mahshid Akhavan [1 ]
Hajaliaskari, Akram [1 ]
Zomorrod, Mina Soufi [1 ,2 ]
机构
[1] Tarbiat Modares Univ TMU, Fac Med Sci, Dept Hematol & Cell Therapy, Tehran, Iran
[2] Tarbiat Modares Univ TMU, Fac Med Sci, Dept Hematol & Cell, PO 14115 111, Tehran, Iran
关键词
Exosomes; Mesenchymal stem cells; Wound healing; ENDOTHELIAL GROWTH-FACTOR; ACTIVATED PROTEIN-C; EXTRACELLULAR VESICLES; ENHANCE ANGIOGENESIS; FACTOR-BETA; FIBROBLAST; INFLAMMATION; MYOFIBROBLAST; MIGRATION; TISSUE;
D O I
10.1016/j.biochi.2023.01.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Skin wound healing is a multifaceted process involving a cascade of molecular and cellular procedures that occur in four different phases: (a) hemostasis, (b) inflammation, (c) proliferation, and (d) tissue remodeling. Prolonged wound healing in skin is still a major challenge in treatment of wounds. Mesenchymal stem cells (MSCs) accelerate cutaneous wound healing through their paracrine activity. Exosomes are one of the key secretory products of MSCs, mimicking the effects of parental MSCs in skin wound healing process. Exosomes are small membrane vesicles (30-150 nm in diameter) that originate from endosomal pathways and transport numerous biomolecules, including DNAs, messenger RNAs, microRNAs, lipids, and proteins. They can be taken up by target cells and release their contents to modulate the activity of recipient cells. Exosomes derived from mesenchymal stem cells (MSC-Exo) reduce inflammation, promote proliferation, inhibit apoptosis, and enhance angiogenesis in skin wound healing process. Therefore, exosomes are emerging as novel cell-cell communication mediators and have opened a novel viewpoint for developing cell-free therapies. This review aims to demonstrate the roles of exosomes in each step of skin wound healing through a comprehensive literature search. (c) 2023 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
引用
收藏
页码:73 / 84
页数:12
相关论文
共 119 条
  • [71] Identification and proteomic profiling of exosomes in human urine
    Pisitkun, T
    Shen, RF
    Knepper, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (36) : 13368 - 13373
  • [72] Exosomes in Human Breast Milk Promote EMT
    Qin, Wenyi
    Tsukasaki, Yoshikazu
    Dasgupta, Santanu
    Mukhopadhyay, Nitai
    Ikebe, Mitsuo
    Sauter, Edward R.
    [J]. CLINICAL CANCER RESEARCH, 2016, 22 (17) : 4517 - 4524
  • [73] Raja, 2007, Front Biosci, V12, P2849
  • [74] The Exosome - A Naturally Secreted Nanoparticle and its Application to Wound Healing
    Rani, Sweta
    Ritter, Thomas
    [J]. ADVANCED MATERIALS, 2016, 28 (27) : 5542 - 5552
  • [75] B lymphocytes secrete antigen-presenting vesicles
    Raposo, G
    Nijman, HW
    Stoorvogel, W
    Leijendekker, R
    Harding, CV
    Melief, CJM
    Geuze, HJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) : 1161 - 1172
  • [76] Wound healing and inflammation: embryos reveal the way to perfect repair
    Redd, MJ
    Cooper, L
    Wood, W
    Stramer, B
    Martin, P
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2004, 359 (1445) : 777 - 784
  • [77] Scars: A review of emerging and currently available therapies
    Reish, Richard G.
    Eriksson, Elof
    [J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 2008, 122 (04) : 1068 - 1078
  • [78] Mechanisms of angiogenesis
    Risau, W
    [J]. NATURE, 1997, 386 (6626) : 671 - 674
  • [79] Robson M C, 2001, Curr Probl Surg, V38, P72, DOI 10.1067/msg.2001.111167
  • [80] miRNA in Wound Inflammation and Angiogenesis
    Roy, Sashwati
    Sen, Chandan K.
    [J]. MICROCIRCULATION, 2012, 19 (03) : 224 - 232