Crucial Role of Extracellular Vesicles in Bronchial Asthma
Extracellular vesicles (EVs) are circulating vesicles secreted by various cell types. EVs are classified into three groups according to size, structural components, and generation process of vesicles: exosomes, microvesicles, and apoptotic bodies. Recently, EVs have been considered to be crucial for...
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| Published in | International journal of molecular sciences Vol. 20; no. 10; p. 2589 |
|---|---|
| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Switzerland
MDPI AG
27.05.2019
MDPI |
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| Online Access | Get full text |
| ISSN | 1422-0067 1661-6596 1422-0067 |
| DOI | 10.3390/ijms20102589 |
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| Abstract | Extracellular vesicles (EVs) are circulating vesicles secreted by various cell types. EVs are classified into three groups according to size, structural components, and generation process of vesicles: exosomes, microvesicles, and apoptotic bodies. Recently, EVs have been considered to be crucial for cell-to-cell communications and homeostasis because they contain intracellular proteins and nucleic acids. Epithelial cells from mice suffering from bronchial asthma (BA) secrete more EVs and suppress inflammation-induced EV production. Moreover, microarray analyses of bronchoalveolar lavage fluid have revealed that several microRNAs are useful novel biomarkers of BA. Mesenchymal stromal cell-derived EVs are possible candidates of novel BA therapy. In this review, we highlight the biologic roles of EVs in BA and review novel EV-targeted therapy to help understanding by clinicians and biologists. |
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| AbstractList | Extracellular vesicles (EVs) are circulating vesicles secreted by various cell types. EVs are classified into three groups according to size, structural components, and generation process of vesicles: exosomes, microvesicles, and apoptotic bodies. Recently, EVs have been considered to be crucial for cell-to-cell communications and homeostasis because they contain intracellular proteins and nucleic acids. Epithelial cells from mice suffering from bronchial asthma (BA) secrete more EVs and suppress inflammation-induced EV production. Moreover, microarray analyses of bronchoalveolar lavage fluid have revealed that several microRNAs are useful novel biomarkers of BA. Mesenchymal stromal cell-derived EVs are possible candidates of novel BA therapy. In this review, we highlight the biologic roles of EVs in BA and review novel EV-targeted therapy to help understanding by clinicians and biologists. [...]EVs have received considerable attention as novel biomarkers and therapeutic targets. [...]by using microarray analyses of BALF, 16 miRNAs containing let-7 and miRNA-200 seem to be useful as novel biomarkers of BA [31]. Alveolar macrophages infected with mycobacteria secrete EVs which contain pathogen-derived proinflammatory molecules and secrete heat-shock proteins (HSP)70, which activates the nuclear factor-κB (NF-κB) pathway by stimulating toll-like receptors (TLRs) [44], leading to the secretion of proinflammatory cytokines [45,46]. [...]alveolar macrophages secrete EVs that contain suppressors of cytokine signaling (SOCS)-1 and SOCS-3, resulting in inhibition of Janus kinase and signal transducers and activators of transcription signaling [47]. [...]these events cause vasodilation, increased vascular permeability, bronchoconstriction, and mucus secretion from airways [56]. Extracellular vesicles (EVs) are circulating vesicles secreted by various cell types. EVs are classified into three groups according to size, structural components, and generation process of vesicles: exosomes, microvesicles, and apoptotic bodies. Recently, EVs have been considered to be crucial for cell-to-cell communications and homeostasis because they contain intracellular proteins and nucleic acids. Epithelial cells from mice suffering from bronchial asthma (BA) secrete more EVs and suppress inflammation-induced EV production. Moreover, microarray analyses of bronchoalveolar lavage fluid have revealed that several microRNAs are useful novel biomarkers of BA. Mesenchymal stromal cell-derived EVs are possible candidates of novel BA therapy. In this review, we highlight the biologic roles of EVs in BA and review novel EV-targeted therapy to help understanding by clinicians and biologists.Extracellular vesicles (EVs) are circulating vesicles secreted by various cell types. EVs are classified into three groups according to size, structural components, and generation process of vesicles: exosomes, microvesicles, and apoptotic bodies. Recently, EVs have been considered to be crucial for cell-to-cell communications and homeostasis because they contain intracellular proteins and nucleic acids. Epithelial cells from mice suffering from bronchial asthma (BA) secrete more EVs and suppress inflammation-induced EV production. Moreover, microarray analyses of bronchoalveolar lavage fluid have revealed that several microRNAs are useful novel biomarkers of BA. Mesenchymal stromal cell-derived EVs are possible candidates of novel BA therapy. In this review, we highlight the biologic roles of EVs in BA and review novel EV-targeted therapy to help understanding by clinicians and biologists. |
| Author | Nishimura, Yoshihiro Umezawa, Kanoko Nagano, Tatsuya Katsurada, Masahiro Hazama, Daisuke Dokuni, Ryota Kiriu, Tatsunori Kobayashi, Kazuyuki |
| AuthorAffiliation | Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan; mskatsu@med.kobe-u.ac.jp (M.K.); rdokuni@med.kobe-u.ac.jp (R.D.); dhazama@med.kobe-u.ac.jp (D.H.); tkiriu@med.kobe-u.ac.jp (T.K.); kanoko03@med.kobe-u.ac.jp (K.U.); kkoba@med.kobe-u.ac.jp (K.K.); nishiy@med.kobe-u.ac.jp (Y.N.) |
| AuthorAffiliation_xml | – name: Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan; mskatsu@med.kobe-u.ac.jp (M.K.); rdokuni@med.kobe-u.ac.jp (R.D.); dhazama@med.kobe-u.ac.jp (D.H.); tkiriu@med.kobe-u.ac.jp (T.K.); kanoko03@med.kobe-u.ac.jp (K.U.); kkoba@med.kobe-u.ac.jp (K.K.); nishiy@med.kobe-u.ac.jp (Y.N.) |
| Author_xml | – sequence: 1 givenname: Tatsuya orcidid: 0000-0003-0790-5139 surname: Nagano fullname: Nagano, Tatsuya – sequence: 2 givenname: Masahiro orcidid: 0000-0003-4655-3367 surname: Katsurada fullname: Katsurada, Masahiro – sequence: 3 givenname: Ryota surname: Dokuni fullname: Dokuni, Ryota – sequence: 4 givenname: Daisuke surname: Hazama fullname: Hazama, Daisuke – sequence: 5 givenname: Tatsunori orcidid: 0000-0001-6877-2005 surname: Kiriu fullname: Kiriu, Tatsunori – sequence: 6 givenname: Kanoko surname: Umezawa fullname: Umezawa, Kanoko – sequence: 7 givenname: Kazuyuki surname: Kobayashi fullname: Kobayashi, Kazuyuki – sequence: 8 givenname: Yoshihiro surname: Nishimura fullname: Nishimura, Yoshihiro |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31137771$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Allergies Angiogenesis Asthma Biomarkers Cell adhesion & migration Chemokines Cytokines Extracellular vesicles Fibroblasts Homeostasis Inflammation Inflammatory diseases Kinases Lymphocytes MicroRNAs Neutrophils Pathogenesis Peptides Proteins Respiratory system Review Roles Transcription factors |
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| Title | Crucial Role of Extracellular Vesicles in Bronchial Asthma |
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