{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T13:56:29Z","timestamp":1791294989520,"version":"4.1.0"},"reference-count":69,"publisher":"Rockefeller University Press","issue":"4","content-domain":{"domain":["rupress.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[1998,11,16]]},"abstract":"<jats:p>P-selectin is an adhesion receptor for leukocytes expressed on activated platelets and endothelial cells. The cytoplasmic domain of P-selectin was shown in vitro to contain signals required for both the sorting of this protein into storage granules and its internalization from the plasma membrane. To evaluate in vivo the role of the regulated secretion of P-selectin, we have generated a mouse that expresses P-selectin lacking the cytoplasmic domain (\u0394CT mice). The deletion did not affect the sorting of P-selectin into \u03b1-granules of platelets but severely compromised the storage of P-selectin in endothelial cells. Unstored P-selectin was proteolytically shed from the plasma membrane, resulting in increased levels of soluble P-selectin in the plasma. The \u0394CT\u2013P-selectin appeared capable of mediating cell adhesion as it supported leukocyte rolling in the mutant mice. However, a secretagogue failed to upregulate leukocyte rolling in the \u0394CT mice, indicating an absence of a releasable storage pool of P-selectin in the endothelium. Furthermore, the neutrophil influx into the inflamed peritoneum was only 30% of the wild-type level 2 h after stimulation. Our results suggest that different sorting mechanisms for P-selectin are used in platelets and endothelial cells and that the storage pool of P-selectin in endothelial cells is functionally important during early stages of inflammation.<\/jats:p>","DOI":"10.1083\/jcb.143.4.1129","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T16:47:50Z","timestamp":1027702070000},"page":"1129-1141","update-policy":"https:\/\/doi.org\/10.1083\/jcb.crossmarkpolicy","source":"Crossref","is-referenced-by-count":94,"title":["Role of P-Selectin Cytoplasmic Domain in Granular Targeting In Vivo and in Early Inflammatory Responses"],"prefix":"10.1083","volume":"143","author":[{"given":"Daqing W.","family":"Hartwell","sequence":"first","affiliation":[{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical 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\u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paul S.","family":"Frenette","sequence":"additional","affiliation":[{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical Institute and \u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"},{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical Institute and \u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Helen","family":"Rayburn","sequence":"additional","affiliation":[{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical Institute and \u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard O.","family":"Hynes","sequence":"additional","affiliation":[{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical Institute and \u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"},{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical Institute and \u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Denisa D.","family":"Wagner","sequence":"additional","affiliation":[{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical Institute and \u00b6Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139"},{"name":"*Center for Blood Research, \u00a7Brigham and Women's Hospital, and \u2021Department of Pathology and \u2016Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115; and **Howard Hughes Medical 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