Emerging roles of extracellular vesicles in COVID-19, a double-edged sword?
Xiaohuan XiaPing YuanYihan LiuYi WangWeijun CaoJialin C ZhengPublished in: Immunology (2021)
The sudden outbreak of SARS-CoV-2-infected disease (COVID-19), initiated from Wuhan, China, has rapidly grown into a global pandemic. Emerging evidence has implicated extracellular vesicles (EVs), a key intercellular communicator, in the pathogenesis and treatment of COVID-19. In the pathogenesis of COVID-19, cells that express ACE2 and CD9 can transfer these viral receptors to other cells via EVs, making recipient cells more susceptible for SARS-CoV-2 infection. Once infected, cells release EVs packaged with viral particles that further facilitate viral spreading and immune evasion, aggravating COVID-19 and its complications. In contrast, EVs derived from stem cells, especially mesenchymal stromal/stem cells, alleviate severe inflammation (cytokine storm) and repair damaged lung cells in COVID-19 by delivery of anti-inflammatory molecules. These therapeutic beneficial EVs can also be engineered into drug delivery platforms or vaccines to fight against COVID-19. Therefore, EVs from diverse sources exhibit distinct effects in regulating viral infection, immune response, and tissue damage/repair, functioning as a double-edged sword in COVID-19. Here, we summarize the recent progress in understanding the pathological roles of EVs in COVID-19. A comprehensive discussion of the therapeutic effects/potentials of EVs is also provided.
Keyphrases
- sars cov
- coronavirus disease
- induced apoptosis
- respiratory syndrome coronavirus
- stem cells
- cell cycle arrest
- immune response
- drug delivery
- magnetic resonance
- endoplasmic reticulum stress
- anti inflammatory
- bone marrow
- magnetic resonance imaging
- risk factors
- angiotensin ii
- cell therapy
- signaling pathway
- inflammatory response
- cell death
- mesenchymal stem cells
- drinking water
- contrast enhanced
- computed tomography
- drug release