Modulation of Immune Responses by Platelet-Derived ADAM10
Platelets have a crucial function in maintaining hemostasis. However, beyond their role in coagulation and thrombus formation, platelets have been implicated to affect various pathophysiological conditions such as infectious diseases, autoimmune disorders, and cancer. It is well-established that pla...
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Published in | Frontiers in immunology Vol. 11; p. 44 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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05.02.2020
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Abstract | Platelets have a crucial function in maintaining hemostasis. However, beyond their role in coagulation and thrombus formation, platelets have been implicated to affect various pathophysiological conditions such as infectious diseases, autoimmune disorders, and cancer. It is well-established that platelets aid local cancer growth by providing growth factors or contributing to cancer angiogenesis. In addition, they promote metastasis, among others by facilitation of tumor cell-extravasation and epithelial-to-mesenchymal-like transition as well as protecting metastasizing cancer cells from immunosurveillance. A variety of membrane-bound and soluble platelet-derived factors are involved in these processes, and many aspects of platelet biology in both health and disease are regulated by platelet-associated metalloproteinases and their inhibitors. Platelets synthesize (i) members of the matrix metalloproteinase (MMP) family and also inhibitors of MMPs such as members of the "tissue inhibitor of metalloproteinases" (TIMP) family as well as (ii) members of the "a disintegrin and metalloproteinase" (ADAM) family including ADAM10. Notably, platelet-associated metalloproteinase activity not only influences functions of platelets themselves: platelets can also induce expression and/or release of metalloproteinases e.g., in leukocytes or cancer cells, and ADAMs are emerging as important components by which platelets directly affect other cell types and function. This review outlines the function of metalloproteinases in platelet biology with a focus on ADAM10 and discusses the role of platelet-derived metalloproteinases in the interaction of platelets with components of the immune system and/or cancer cells. |
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AbstractList | Platelets have a crucial function in maintaining hemostasis. However, beyond their role in coagulation and thrombus formation, platelets have been implicated to affect various pathophysiological conditions such as infectious diseases, autoimmune disorders, and cancer. It is well-established that platelets aid local cancer growth by providing growth factors or contributing to cancer angiogenesis. In addition, they promote metastasis, among others by facilitation of tumor cell-extravasation and epithelial-to-mesenchymal-like transition as well as protecting metastasizing cancer cells from immunosurveillance. A variety of membrane-bound and soluble platelet-derived factors are involved in these processes, and many aspects of platelet biology in both health and disease are regulated by platelet-associated metalloproteinases and their inhibitors. Platelets synthesize (i) members of the matrix metalloproteinase (MMP) family and also inhibitors of MMPs such as members of the "tissue inhibitor of metalloproteinases" (TIMP) family as well as (ii) members of the "a disintegrin and metalloproteinase" (ADAM) family including ADAM10. Notably, platelet-associated metalloproteinase activity not only influences functions of platelets themselves: platelets can also induce expression and/or release of metalloproteinases e.g., in leukocytes or cancer cells, and ADAMs are emerging as important components by which platelets directly affect other cell types and function. This review outlines the function of metalloproteinases in platelet biology with a focus on ADAM10 and discusses the role of platelet-derived metalloproteinases in the interaction of platelets with components of the immune system and/or cancer cells. |
Author | Maurer, Stefanie Kropp, Korbinian N Kopp, Hans-Georg Salih, Helmut R |
AuthorAffiliation | 2 DFG Cluster of Excellence 2180 ‘Image-guided and Functional Instructed Tumor Therapy’ (IFIT), University of Tuebingen , Tubingen , Germany 4 Departments of Molecular Oncology and Thoracic Oncology, Robert-Bosch-Hospital Stuttgart , Stuttgart , Germany 1 Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tuebingen , Tuebingen , Germany 3 Department of Radiology, Memorial Sloan Kettering Cancer Center , New York, NY , United States 5 Department of Hematology, Medical Oncology and Pneumology, University Medical Center of Mainz , Mainz , Germany |
AuthorAffiliation_xml | – name: 5 Department of Hematology, Medical Oncology and Pneumology, University Medical Center of Mainz , Mainz , Germany – name: 1 Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tuebingen , Tuebingen , Germany – name: 2 DFG Cluster of Excellence 2180 ‘Image-guided and Functional Instructed Tumor Therapy’ (IFIT), University of Tuebingen , Tubingen , Germany – name: 4 Departments of Molecular Oncology and Thoracic Oncology, Robert-Bosch-Hospital Stuttgart , Stuttgart , Germany – name: 3 Department of Radiology, Memorial Sloan Kettering Cancer Center , New York, NY , United States |
Author_xml | – sequence: 1 givenname: Stefanie surname: Maurer fullname: Maurer, Stefanie organization: Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, United States – sequence: 2 givenname: Hans-Georg surname: Kopp fullname: Kopp, Hans-Georg organization: Departments of Molecular Oncology and Thoracic Oncology, Robert-Bosch-Hospital Stuttgart, Stuttgart, Germany – sequence: 3 givenname: Helmut R surname: Salih fullname: Salih, Helmut R organization: DFG Cluster of Excellence 2180 'Image-guided and Functional Instructed Tumor Therapy' (IFIT), University of Tuebingen, Tubingen, Germany – sequence: 4 givenname: Korbinian N surname: Kropp fullname: Kropp, Korbinian N organization: Department of Hematology, Medical Oncology and Pneumology, University Medical Center of Mainz, Mainz, Germany |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32117229$$D View this record in MEDLINE/PubMed |
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Keywords | ADAM10 ectodomain shedding immune evasion tumor platelets |
Language | English |
License | Copyright © 2020 Maurer, Kopp, Salih and Kropp. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Edited by: Armando Rossello, University of Pisa, Italy Reviewed by: Andreas Ludwig, RWTH Aachen University, Germany; William Parks, Cedars-Sinai Medical Center, United States This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology |
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SubjectTerms | ADAM10 ADAM10 Protein - metabolism Amyloid Precursor Protein Secretases - metabolism Animals Blood Platelets - immunology ectodomain shedding Humans immune evasion Immunity Immunology Matrix Metalloproteinases - metabolism Membrane Proteins - metabolism Mice Neoplasms - immunology Neoplasms - metabolism platelets Proteolysis tumor Tumor Escape |
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Title | Modulation of Immune Responses by Platelet-Derived ADAM10 |
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