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
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