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Page 26                                              Extracell Vesicles Circ Nucleic Acids 2020;1:20-56  I  http://dx.doi.org/10.20517/evcna.2020.10

               Abstracts: Since the severe acute respiratory syndrome corona virus 2 (SARS-CoV-2) was declared a
               pandemic in mid-March of 2020 by the World Health Origination (WHO), laboratories around the
                                                                          [1]
               world started research into diagnostics, therapeutics, and treatments . In recent years, the importance of
               extracellular vesicles (EVs) in the pathogenesis of viral infections have been found in the cases of many viral
               pathogens including few DNA and RNA viruses including human T-cell leukemia virus-1 (HTLV-1) and
                                                    [2,3]
               human immunodeficiency virus-1 (HIV-1) . EVs from HIV-1 infected cells on uninfected macrophages
                                                                 [3]
               induces an increase in the proinflammatory cytokines . While EVs from HTLV-1 infected cells on
               uninfected recipient cells promoted the localization and cellular contact by cells, this directly influences
                                                                                              [2]
               the pathogenesis of HTLV-1 as the virus mainly infects other cells by cell to cell contact . Similar to
               retroviruses, coronaviruses are also positive strand RNA viruses, except they replicate in the cytoplasm and
               may regulate chromosomal DNA depending on the strain of virus. We have recently began working on
               beta- coronaviruses, including OC43 (BSL2 strain) and SARS-CoV-2 (BSL3 strain). Our initial experiments
               focus on isolation of EVs away from virions using either an iodixanol gradients or Izon sizing columns.
               We have successfully separated the two from one another mainly due to their density and potentially size
               differences. We found that EVs from multiple coronaviruses are not infectious and viral particles treated
               with UV irradiation are also not infectious. We also have found that coronavirus EVs caused T-cell death,
               which may corelate with lymphopenia observed in COVID patients. Along these lines coronavirus EVs can
               activate other viral genes (i.e., HIV-1 or HTLV-1) when these genes are integrated into the genome, further
               implying that these EVS regulate chromosomal gene expression. Finally, the mechanism(s) of how these
               EVs may cause such diverse effects on T-cells and other viral gene expression will be discussed.


               REFERENCES
               1.   Cucinotta D, Vanelli M. WHO Declares COVID-19 a Pandemic. Acta Biomed 2020;91:157-60.
               2.   Pinto DO, DeMarino C, Pleet ML, et al. HTLV-1 extracellular vesicles promote cell-to-cell contact. Front Microbiol 2019;10:2147.
               3.   Sampey GC, Saifuddin M, Schwab A, et al. Exosomes from HIV-1-infected cells stimulate production of pro-inflammatory cytokines
                   through trans-activating response (TAR) RNA. J Biol Chem 2016;291:1251-66.


               7. Use of stem cell extracellular vesicles as a holistic approach towards CNS repair


                                                        3
                                        1,2
                                                                                                  4
                                                                                   4
                                                                     3
               Authors: Heather Branscome , Siddhartha Paul , Dezhong Yin , Weidong Zhou , Lance A. Liotta ,
                             1,
               Fatah Kashanchi *
               E-mail: hbranscome@atcc.org
               Affiliations:
               1 Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA,
               USA.
               2 American Type Culture Collection (ATCC), Manassas, VA, USA.
               3 ATCC Cell Systems, Gaithersburg, MD, USA.
               4 Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
               Abstracts: Neurological diseases and disorders are leading causes of death and disability worldwide. Many
               of these pathologies are associated with high levels of neuroinflammation and irreparable tissue damage.
               We have previously shown that extracellular vesicles (EVs) from infected cells contain viral by products
                                                                                                       [1-3]
               (non-coding RNAs and proteins) and that these EVs can exert deleterious effects on recipient cells .
               Therefore, in the context of neurotrophic viruses EVs may contribute to or perpetuate processes relating
               to neuroinflammation and neurodegeneration. Due to their multipotent properties, stem cells have broad
               applications for tissue repair; additionally, stem cells have been shown to possess both immunomodulatory
               and neuroprotective properties. In recent years it has been well-established that stem cell EVs play a critical
               role in the functionality associated with stem cells. The diverse biological cargo contained within these
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