Title | Autophagy in Platelets. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Banerjee M, Huang Y, Ouseph MM, Joshi S, Pokrovskaya I, Storrie B, Zhang J, Whiteheart SW, Wang QJun |
Journal | Methods Mol Biol |
Volume | 1880 |
Pagination | 511-528 |
Date Published | 2019 |
ISSN | 1940-6029 |
Keywords | Animals, Autophagosomes, Autophagy, Blood Platelets, Green Fluorescent Proteins, Healthy Volunteers, Hemostasis, Humans, Intravital Microscopy, Megakaryocytes, Mice, Mice, Transgenic, Microscopy, Confocal, Microscopy, Electron, Transmission, Microtubule-Associated Proteins |
Abstract | Anucleate platelets are produced by fragmentation of megakaryocytes. Platelets circulate in the bloodstream for a finite period: upon vessel injury, they are activated to participate in hemostasis; upon senescence, unused platelets are cleared. Platelet hypofunction leads to bleeding. Conversely, pathogenic platelet activation leads to occlusive events that precipitate strokes and heart attacks. Recently, we and others have shown that autophagy occurs in platelets and is important for platelet production and normal functions including hemostasis and thrombosis. Due to the unique properties of platelets, such as their lack of nuclei and their propensity for activation, methods for studying platelet autophagy must be specifically tailored. Here, we describe useful methods for examining autophagy in both human and mouse platelets. |
DOI | 10.1007/978-1-4939-8873-0_32 |
Alternate Journal | Methods Mol Biol |
PubMed ID | 30610718 |
PubMed Central ID | PMC7039316 |
Grant List | R01 HL119393 / HL / NHLBI NIH HHS / United States R01 HL138179 / HL / NHLBI NIH HHS / United States R01 HL056652 / HL / NHLBI NIH HHS / United States I01 BX003877 / BX / BLRD VA / United States 15PRE25550020 / AHA / American Heart Association-American Stroke Association / United States R56 HL119393 / HL / NHLBI NIH HHS / United States |
Related Faculty:
Madhu Ouseph, M.D., Ph.D.