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 inFrontiers in immunology Vol. 11; p. 44
Main Authors Maurer, Stefanie, Kopp, Hans-Georg, Salih, Helmut R, Kropp, Korbinian N
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 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.
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.
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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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Snippet Platelets have a crucial function in maintaining hemostasis. However, beyond their role in coagulation and thrombus formation, platelets have been implicated...
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StartPage 44
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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