Intracellular Trafficking, Localization, and Mobilization of Platelet-Borne Thiol Isomerases. Issue 6 (June 2016)

• Record Type: Journal Article
• Authors: Crescente, Marilena; Pluthero, Fred G.; Li, Ling; Lo, Richard W.; Walsh, Tony G.; Schenk, Michael P.; Holbrook, Lisa M.; Louriero, Silvia; Ali, Marfoua S.; Vaiyapuri, Sakthivel; Falet, Hervé; Jones, Ian M.; Poole, Alastair W.; Kahr, Walter H.A.; Gibbins, Jonathan M.
• Is Part Of: Arteriosclerosis, thrombosis, and vascular biology. Volume 36:Issue 6(2016)
• Publication Date: 2016-06
• Subjects: blood platelets -- megakaryocytes -- membrane fusion -- protein disulfide isomerases -- secretory vesicles; Arteriosclerosis -- Periodicals; Thrombosis -- Periodicals; Blood-vessels -- Pathophysiology -- Periodicals; Electronic journals; 616.13
• DOI: 10.1161/ATVBAHA.116.307461
• Languages: English
• ISSNs: 1079-5642

Abstract

Abstract : Objective—: Thiol isomerases facilitate protein folding in the endoplasmic reticulum, and several of these enzymes, including protein disulfide isomerase and ERp57, are mobilized to the surface of activated platelets, where they influence platelet aggregation, blood coagulation, and thrombus formation. In this study, we examined the synthesis and trafficking of thiol isomerases in megakaryocytes, determined their subcellular localization in platelets, and identified the cellular events responsible for their movement to the platelet surface on activation. Approach and Results—: Immunofluorescence microscopy imaging was used to localize protein disulfide isomerase and ERp57 in murine and human megakaryocytes at various developmental stages. Immunofluorescence microscopy and subcellular fractionation analysis were used to localize these proteins in platelets to a compartment distinct from known secretory vesicles that overlaps with an inner cell-surface membrane region defined by the endoplasmic/sarcoplasmic reticulum proteins calnexin and sarco/endoplasmic reticulum calcium ATPase 3. Immunofluorescence microscopy and flow cytometry were used to monitor thiol isomerase mobilization in activated platelets in the presence and absence of actin polymerization (inhibited by latrunculin) and in the presence or absence of membrane fusion mediated by Munc13-4 (absent in platelets from Unc13d Jinx mice). Conclusions—: Platelet-borne thiol isomerases are trafficked independently of secretory granule contents in megakaryocytes and become concentrated in a subcellular compartment near the inner surface of the platelet outer membrane corresponding to the sarco/endoplasmic reticulum of these cells. Thiol isomerases are mobilized to the surface of activated platelets via a process that requires actin polymerization but not soluble N-ethylmaleimide–sensitive fusion protein attachment receptor/Munc13-4–dependent vesicular–plasma membrane fusion. Abstract : Supplemental Digital Content is available in the text.