Literature DB >> 32777963

Wharton's Jelly Mesenchymal Stem Cells Exosomes and Conditioned Media Increased Neutrophil Lifespan and Phagocytosis Capacity.

Mahsa Taghavi-Farahabadi1, Mohammad Mahmoudi2, Nima Rezaei1,3,4, Seyed Mahmoud Hashemi5,6,7.   

Abstract

Neutrophils are the first cells involved in inflammation and pathogen elimination, but they have a short lifespan. So, strategies for enhancing neutrophil lifespan and activities can be useful in many situations such as patients with immunodeficiencies. Previous researches demonstrated that mesenchymal stem cell (MSC) has anti-apoptotic effects on neutrophils. These multipotent cells have immunomodulatory properties and can be isolated from different tissues. MSCs isolated from Wharton's jelly (WJ-MSCs), a mucosal connective tissue of the umbilical cord, may be better candidates than MSCs obtained from bone marrow or adipose tissue, because WJ-MSCs are younger and protected from damages that are resulted from aging, environmental toxins, and diseases. In addition, they have high proliferative capacity, easier accessibility, and more abundance. It was shown that following in vitro expansion, they are more effective than other sources of MSCs. Cell to cell contact or secretion of soluble factors and exosomes are the main approaches of MSCs in applying their effects. Exosomes and conditioned media (CM) were prepared from WJ-MSCs. Then, neutrophils were isolated and cultured with medium, CM, or exosomes. Then, neutrophil respiratory burst, apoptosis, and phagocytosis capacity were assessed by NBT assay, Annexin V-PI method, and Giemsa staining, respectively. Both treatments improved neutrophil lifespan and phagocytosis. Only MSC-CM could enhance neutrophil respiratory burst. This research demonstrated that MSC-exosomes and CM have protective effects on neutrophil function and lifespan. It can be concluded that MSC mediators can be responsible factors for protective functions of MSCs on neutrophils.

Entities:  

Keywords:  Apoptosis; conditioned media; exosomes; mesenchymal stem cells; neutrophils

Mesh:

Substances:

Year:  2020        PMID: 32777963     DOI: 10.1080/08820139.2020.1801720

Source DB:  PubMed          Journal:  Immunol Invest        ISSN: 0882-0139            Impact factor:   3.657


  6 in total

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Authors:  Hongbing Lin; Huishan Chen; Xuetao Zhao; Tong Ding; Yawei Wang; Zhen Chen; Yue Tian; Peipei Zhang; Yuqin Shen
Journal:  J Transl Med       Date:  2022-06-21       Impact factor: 8.440

2.  News About the Extracellular Vesicles from Mesenchymal Stem Cells: Functions, Therapy and Protection from COVID-19.

Authors:  Jacopo Meldolesi
Journal:  J Exp Pathol (Wilmington)       Date:  2021

Review 3.  Clinical Translational Potentials of Stem Cell-Derived Extracellular Vesicles in Type 1 Diabetes.

Authors:  Wei Hu; Xiang Song; Haibo Yu; Jingyu Sun; Hongjun Wang; Yong Zhao
Journal:  Front Endocrinol (Lausanne)       Date:  2022-01-12       Impact factor: 5.555

4.  Procollagen C-Endopeptidase Enhancer 2 Secreted by Tonsil-Derived Mesenchymal Stem Cells Increases the Oxidative Burst of Promyelocytic HL-60 Cells.

Authors:  Hee-Soo Yoon; Hee-Yeon Kim; Kyung-Ah Cho; Yu-Hee Kim; So-Youn Woo; Han-Su Kim; Jihee-Lee Kang; Kyung-Ha Ryu; Joo-Won Park
Journal:  Biology (Basel)       Date:  2022-02-07

Review 5.  TA-MSCs, TA-MSCs-EVs, MIF: their crosstalk in immunosuppressive tumor microenvironment.

Authors:  Zhenghou Zhang; Xiangyu Zhou; Jinshuai Guo; Fusheng Zhang; Yiping Qian; Guang Wang; Meiqi Duan; Yutian Wang; Haiying Zhao; Zhi Yang; Zunpeng Liu; Xiaofeng Jiang
Journal:  J Transl Med       Date:  2022-07-16       Impact factor: 8.440

6.  MicroRNA-Enriched Exosomes from Different Sources of Mesenchymal Stem Cells Can Differentially Modulate Functions of Immune Cells and Neurogenesis.

Authors:  Naina Soni; Suchi Gupta; Surender Rawat; Vishnu Krishnakumar; Sujata Mohanty; Arup Banerjee
Journal:  Biomedicines       Date:  2021-12-30
  6 in total

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