Host derived exosomes-pathogens interactions: Potential functions of exosomes in pathogen infection

被引:66
作者
Wang, Jianjun [1 ]
Yao, Yongliang [1 ]
Chen, Xiaomei [2 ]
Wu, Jianhong [1 ]
Gu, Tao [1 ]
Tang, Xin [1 ]
机构
[1] Jiangsu Univ, Kunshan Peoples Hosp 1, Dept Clin Lab, Kunshan 215300, Peoples R China
[2] Jiangyin Peoples Hosp, Dept Clin Lab, Jiangyin 214400, Peoples R China
关键词
Exosomes; Pathogen; Bacteria; Immune regulation; Inflammatory response; HEPATITIS-C VIRUS; EPSTEIN-BARR-VIRUS; EXTRACELLULAR VESICLES; MYCOBACTERIUM-TUBERCULOSIS; MEMBRANE-VESICLES; ENDOTHELIAL-CELLS; MESSENGER-RNAS; T-CELLS; TRANSMISSION; RELEASE;
D O I
10.1016/j.biopha.2018.09.174
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
As bilayer vesicular corpuscles secreted by different living cells, exosomes can be found in diverse body fluids and are rich in lipids, proteins, nucleic acids and other complicated components. Exosomes offer a potent mechanism for participation in intercellular transportation, such as targeted transmission of inclusions to nearby or distant cells or tissues, and assistance in intercellular information communication to change physiological functions and properties. Exosomes take part in antigen presentation for activation of immune cells and stimulate the release of inflammatory factors and the expression of immune molecules, thus modulating the immune responses of host cells. In the microbial infection of host cells, exosomes can strengthen innate and specific immune responses and thereby the immune resistance against the invading microbes through natural killer cells, macrophages and activated T cells by the presentation of pathogens including viral factors and bacteria, but exosomes are also capable of immunosuppression during pathogens infection. Exosomes are considerably valuable in research and clinical defense of microbial infection, given their biological activities in intercellular transportation, information communication and cell-mediated immunity modulation after microbial infection.
引用
收藏
页码:1451 / 1459
页数:9
相关论文
共 98 条
[1]   Human Galectin-9 Is a Potent Mediator of HIV Transcription and Reactivation [J].
Abdel-Mohsen, Mohamed ;
Chavez, Leonard ;
Tandon, Ravi ;
Chew, Glen M. ;
Deng, Xutao ;
Danesh, Ali ;
Keating, Sheila ;
Lanteri, Marion ;
Samuels, Michael L. ;
Hoh, Rebecca ;
Sacha, Jonah B. ;
Norris, Philip J. ;
Niki, Toshiro ;
Shikuma, Cecilia M. ;
Hirashima, Mitsuomi ;
Deeks, Steven G. ;
Ndhlovu, Lishomwa C. ;
Pillai, Satish K. .
PLOS PATHOGENS, 2016, 12 (06)
[2]   Development of Small Molecules with a Noncanonical Binding Mode to HIV-1 Trans Activation Response (TAR) RNA [J].
Abulwerdi, Fardokht A. ;
Shortridge, Matthew D. ;
Sztuba-Solinska, Joanna ;
Wilson, Robert ;
Le Grice, Stuart F. J. ;
Varani, Gabriele ;
Schneekloth, John S., Jr. .
JOURNAL OF MEDICINAL CHEMISTRY, 2016, 59 (24) :11148-11160
[3]   Exosome Biogenesis, Regulation, and Function in Viral Infection [J].
Alenquer, Marta ;
Amorim, Maria Joao .
VIRUSES-BASEL, 2015, 7 (09) :5066-5083
[4]  
Anderson L, 2016, METHODS MOL BIOL, V1442, P195, DOI 10.1007/978-1-4939-3687-8_14
[5]   Exosomes in Viral Disease [J].
Anderson, Monique R. ;
Kashanchi, Fatah ;
Jacobson, Steven .
NEUROTHERAPEUTICS, 2016, 13 (03) :535-546
[6]   Exosomes: an overview of biogenesis, composition and role in ovarian cancer [J].
Beach, Allison ;
Zhang, Huang-Ge ;
Ratajczak, Mariusz Z. ;
Kakar, Sham S. .
JOURNAL OF OVARIAN RESEARCH, 2014, 7
[7]   Exosomes released from macrophages infected with intracellular pathogens stimulate a proinflammatory response in vitro and in vivo [J].
Bhatnagar, Sanchita ;
Shinagawa, Kazuhiko ;
Castellino, Francis J. ;
Schorey, Jeff Rey S. .
BLOOD, 2007, 110 (09) :3234-3244
[8]   Exosomes from Hepatitis C Infected Patients Transmit HCV Infection and Contain Replication Competent Viral RNA in Complex with Ago2-miR122-HSP90 [J].
Bukong, Terence N. ;
Momen-Heravi, Fatemeh ;
Kodys, Karen ;
Bala, Shashi ;
Szabo, Gyongyi .
PLOS PATHOGENS, 2014, 10 (10)
[9]   Quantitation of Plasmacytoid Dendritic Cells in Chronic Hepatitis B Patients with HBeAg Positivity During PEG-IFN and Entecavir Therapy [J].
Cao, Wei-Hua ;
Li, Ming-Hui ;
Pan, Calvin Q. ;
Lu, Yao ;
Zhang, Lu ;
Ran, Chong-Ping ;
Wu, Shu-Ling ;
Hua, Wen-Hao ;
Liu, Shun-Ai ;
Shen, Ge ;
Chang, Min ;
Liu, Ru-Yu ;
Hao, Hong-Xiao ;
Hu, Lei-Ping ;
Xie, Yao .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2018, 38 (05) :197-205
[10]   Exosomes: From Functions in Host-Pathogen Interactions and Immunity to Diagnostic and Therapeutic Opportunities [J].
Carriere, Jessica ;
Barnich, Nicolas ;
Hang Thi Thu Nguyen .
REVIEWS OF PHYSIOLOGY, BIOCHEMISTRY AND PHARMACOLOGY, VOL 172, 2016, 172 :39-75