TY - JOUR
T1 - Immunocytochemical localization of the chemokines RANTES and MIP-1α within human platelets and their release during storage
AU - Klinger, M. H.F.
AU - Wilhelm, D.
AU - Bubel, S.
AU - Sticherling, M.
AU - Schröder, J. M.
AU - Kühnel, W.
N1 - Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 1995
Y1 - 1995
N2 - The cytokines RANTES and MIP-1α are 8-kD peptides which belong to the C-C subfamily of chemokines. They are both potent chemotactic factors for basophils and eosinophils. Apart from lymphocytes, the RANTES peptides was recently shown to be released from human platelets stimulated with thrombin [Kameyoshi et al: J Exp Med 1992:176:587-592]. Employing postembedding immunocytochemistry, we could detect RANTES and for the first time also MIP-���� within the ����-granules of human platelets. To date, MIP-1α was not reported to occur in platelets. In slightly activated platelets, as found in stored platelet concentrates (PC), label for RANTES and MIP-1α could also be observed within cisterns of the open canalicular system and on the plasma membrane, indicating a release of both peptides. These findings were confirmed by in vitro studies in PC, by investigation of RANTES and MIP-lα release into the suspending medium. Over a period of 8 days, RANTES was steadily released in relatively high amounts, whereas MIP-1α was measured in rather small amounts in the suspending medium. As RANTES and MIP-1α, besides their chemotactic activity on eosinophils and basophils, are able to mediate the release of histamine, it is tempting to speculate about a participation of platelets in inflammatory reactions in which eosinophils and basophils are involved.
AB - The cytokines RANTES and MIP-1α are 8-kD peptides which belong to the C-C subfamily of chemokines. They are both potent chemotactic factors for basophils and eosinophils. Apart from lymphocytes, the RANTES peptides was recently shown to be released from human platelets stimulated with thrombin [Kameyoshi et al: J Exp Med 1992:176:587-592]. Employing postembedding immunocytochemistry, we could detect RANTES and for the first time also MIP-���� within the ����-granules of human platelets. To date, MIP-1α was not reported to occur in platelets. In slightly activated platelets, as found in stored platelet concentrates (PC), label for RANTES and MIP-1α could also be observed within cisterns of the open canalicular system and on the plasma membrane, indicating a release of both peptides. These findings were confirmed by in vitro studies in PC, by investigation of RANTES and MIP-lα release into the suspending medium. Over a period of 8 days, RANTES was steadily released in relatively high amounts, whereas MIP-1α was measured in rather small amounts in the suspending medium. As RANTES and MIP-1α, besides their chemotactic activity on eosinophils and basophils, are able to mediate the release of histamine, it is tempting to speculate about a participation of platelets in inflammatory reactions in which eosinophils and basophils are involved.
UR - http://www.scopus.com/inward/record.url?scp=0029036311&partnerID=8YFLogxK
U2 - 10.1159/000237097
DO - 10.1159/000237097
M3 - Journal articles
C2 - 7542516
AN - SCOPUS:0029036311
SN - 1018-2438
VL - 107
SP - 541
EP - 546
JO - International Archives of Allergy and Immunology
JF - International Archives of Allergy and Immunology
IS - 4
ER -