Neutrophil-derived S100 calcium-binding proteins A8/A9 promote reticulated thrombocytosis and atherogenesis in diabetes

• Published in: The Journal of clinical investigation Vol. 127; no. 6; pp. 2133 - 2147
• Main Authors: Kraakman, Michael J., Lee, Man K.S., Al-Sharea, Annas, Dragoljevic, Dragana, Barrett, Tessa J., Montenont, Emilie, Basu, Debapriya, Heywood, Sarah, Kammoun, Helene L., Flynn, Michelle, Whillas, Alexandra, Hanssen, Nordin M.J., Febbraio, Mark A., Westein, Erik, Fisher, Edward A., Chin-Dusting, Jaye, Cooper, Mark E., Berger, Jeffrey S., Goldberg, Ira J., Nagareddy, Prabhakara R., Murphy, Andrew J.
• Format: Journal Article
• Language: English
• Published: United States American Society for Clinical Investigation 01.06.2017
• Subjects: Advanced glycosylation end products; Animals; Antiplatelet therapy; Atherogenesis; Atherosclerosis; Atherosclerosis - immunology; Atherosclerosis - metabolism; Biomedical research; Blood platelets; Blood Platelets - physiology; Bone marrow; Calcium; Calcium binding proteins; Calgranulin A - physiology; Calgranulin B - physiology; Cardiovascular disease; Cardiovascular diseases; Cell proliferation; Chemokines; Complications and side effects; Cytokines; Development and progression; Diabetes; Diabetes mellitus; Diabetes Mellitus, Experimental - complications; Diabetes Mellitus, Experimental - immunology; Diabetes Mellitus, Experimental - metabolism; Glucose; Glycosylation; Health aspects; Hemoglobin; Hepatocytes; Humans; Hyperglycemia; Inflammation; Interleukin 6; Ischemia; Kupffer cells; Leukocytes (neutrophilic); Lupus; Male; Megakaryocytes; Mice, Inbred C57BL; Mice, Knockout; Mice, Obese; Mortality; Myocardial ischemia; Na+/glucose cotransporter; Neutrophils; Neutrophils - metabolism; Osteoprogenitor cells; Platelets; Proteins; Rodents; Sodium; Stem cells; Thrombocytosis; Thrombocytosis - immunology; Thrombocytosis - metabolism; Thrombosis
• ISSN: 0021-9738; 1558-8238; 1558-8238
• DOI: 10.1172/JCI92450

Platelets play a critical role in atherogenesis and thrombosis-mediated myocardial ischemia, processes that are accelerated in diabetes. Whether hyperglycemia promotes platelet production and whether enhanced platelet production contributes to enhanced atherothrombosis remains unknown. Here we found that in response to hyperglycemia, neutrophil-derived S100 calcium-binding proteins A8/A9 (S100A8/A9) interact with the receptor for advanced glycation end products (RAGE) on hepatic Kupffer cells, resulting in increased production of IL-6, a pleiotropic cytokine that is implicated in inflammatory thrombocytosis. IL-6 acts on hepatocytes to enhance the production of thrombopoietin, which in turn interacts with its cognate receptor c-MPL on megakaryocytes and bone marrow progenitor cells to promote their expansion and proliferation, resulting in reticulated thrombocytosis. Lowering blood glucose using a sodium-glucose cotransporter 2 inhibitor (dapagliflozin), depleting neutrophils or Kupffer cells, or inhibiting S100A8/A9 binding to RAGE (using paquinimod), all reduced diabetes-induced thrombocytosis. Inhibiting S100A8/A9 also decreased atherogenesis in diabetic mice. Finally, we found that patients with type 2 diabetes have reticulated thrombocytosis that correlates with glycated hemoglobin as well as increased plasma S100A8/A9 levels. These studies provide insights into the mechanisms that regulate platelet production and may aid in the development of strategies to improve on current antiplatelet therapies and to reduce cardiovascular disease risk in diabetes.