Role of MRP4 (ABCC4) in Platelet Adenine Nucleotide-Storage Evidence from Patients with Delta-Storage Pool Deficiencies

被引:38
作者
Jedlitschky, Gabriele [1 ]
Cattaneo, Marco [3 ,4 ,5 ]
Lubenow, Lena E. [2 ]
Rosskopf, Dieter
Lecchi, Anna [3 ]
Artoni, Andrea [3 ]
Motta, Giovanna [3 ]
Niessen, Juliane
Kroemer, Heyo K.
Greinacher, Andreas [2 ]
机构
[1] Ernst Moritz Arndt Univ Greifswald, Inst Pharmakol, Dept Pharmacol, Res Ctr Pharmacol & Expt Therapeut, D-17487 Greifswald, Germany
[2] Ernst Moritz Arndt Univ Greifswald, Dept Immunol & Transfus Med, D-17487 Greifswald, Germany
[3] Univ Milan, Dipartimento Med & Specialita Med, Milan, Italy
[4] Univ Milan, IRCCS, Fdn Osped Maggiore Mangiagalli & Regina Elena, Milan, Italy
[5] Univ Milan, Unita Ematol & Trombosi, Osped San Paolo, Milan, Italy
关键词
HERMANSKY-PUDLAK-SYNDROME; DENSE GRANULES; EXPRESSION; CLONING; ADP;
D O I
10.2353/ajpath.2010.090425
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We previously showed that die MRP4 (ABCC4) transporter is expressed in human platelet delta-granules, and may he involved in ADP transport. We now demonstrate by immunoblotting and immunofluorescence microscopy that platelet MRP4 is absent in two patients with a platelet delta-storage pool deficiency (delta-SPD)-like phenotype with reduced platelet adenine nucleotide (AN) but normal serotonin levels, whereas their other membrane marker proteins of platelet granules were normally expressed and localized. in these patients, MRP4 was present in lymphocytes, and the coding region of their MRP4/ABCC4 gene did not show any mutation that explained the lack of expression. In platelets with "classic" delta-SPD (low AN and serotonin levels), MRP4 was quantitatively (immunoblot) normal, but, like other delta-granules membrane marker proteins (eg, LAMP2), was mostly displaced from delta-granules to patches at the plasma membrane, suggesting that platelets with classic delta-SPD have an abnormality that impairs the assembly of normal delta-granules. Thus, defective expression of platelet MRP4 is associated with selective defect in AN storage. The genetic basis of the new delta-SPD phenotype remains to be elucidated. (Am J Pathol 2010, 176:1097-1103: DOI: 10.2353/ajpath.2010.090425)
引用
收藏
页码:1097 / 1103
页数:7
相关论文
共 23 条
[1]   ERM-merlin and EBP50 protein families in plasma membrane organization and function [J].
Bretscher, A ;
Chambers, D ;
Nguyen, R ;
Reczek, D .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 :113-+
[2]  
CALLAN MB, 1995, THROMB HAEMOSTASIS, V74, P949
[3]   SUSTAINED CORRECTION OF THE BLEEDING-TIME IN AN AFIBRINOGENEMIC PATIENT AFTER INFUSION OF FRESH-FROZEN PLASMA [J].
CATTANEO, M ;
BETTEGA, D ;
LOMBARDI, R ;
LECCHI, A ;
MANNUCCI, PM .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 82 (02) :388-390
[4]   Inherited platelet-based bleeding disorders [J].
Cattaneo, M .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (07) :1628-1636
[5]   Platelets from a patient heterozygous for the defect of P2CYC receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores -: Further evidence that some cases of platelet 'primary secretion defect' are heterozygous for a defect of P2CYC receptors [J].
Cattaneo, M ;
Lecchi, A ;
Lombardi, R ;
Gachet, C ;
Zighetti, ML .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (11) :E101-E106
[6]   Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the β3A subunit of the AP-3 adaptor [J].
Dell'Angelica, EC ;
Shotelersuk, V ;
Aguilar, RC ;
Gahl, WA ;
Bonifacino, JS .
MOLECULAR CELL, 1999, 3 (01) :11-21
[7]   EXPRESSION CLONING OF A RESERPINE-SENSITIVE VESICULAR MONOAMINE TRANSPORTER [J].
ERICKSON, JD ;
EIDEN, LE ;
HOFFMAN, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) :10993-10997
[8]   Review article: serotonin receptors and transporters - roles in normal and abnormal gastrointestinal motility [J].
Gershon, MD .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 20 :3-14
[9]   Molecular defects that affect platelet dense granules [J].
Gunay-Aygun, M ;
Huizing, M ;
Gahl, WA .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2004, 30 (05) :537-547
[10]   ALBINISM ASSOCIATED WITH HEMORRHAGIC DIATHESIS AND UNUSUAL PIGMENTED RETICULAR CELLS IN THE BONE MARROW - REPORT OF 2 CASES WITH HISTOCHEMICAL STUDIES [J].
HERMANSKY, F ;
PUDLAK, P .
BLOOD, 1959, 14 (02) :162-169