Absence of GPIbα is responsible for aberrant membrane development during megakaryocyte maturation:: Ultrastructural study using a transgenic model

被引:67
作者
Poujol, CR
Ware, J
Nieswandt, B
Nurden, AT
Nurden, P
机构
[1] Hop Cardiol, UMR 5533 CNRS, Hematol Lab, F-33604 Pessac, France
[2] Scripps Res Inst, Roon Res Ctr Arteriosclerosis & Thrombosis, Div Expt Hemostasis & Thrombosis, Dept Mol & Expt Med, La Jolla, CA USA
[3] Scripps Res Inst, Roon Res Ctr Arteriosclerosis & Thrombosis, Div Expt Hemostasis & Thrombosis, Dept Vasc Biol, La Jolla, CA USA
[4] Univ Witten Herdecke, Dept Mol Oncol, Wuppertal, Germany
关键词
D O I
10.1016/S0301-472X(02)00774-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The glycoprotein Ib/IX/V complex (GPIb-IX-V) mediates platelet attachment to von Willebrand factor in exposed subendothelium. Molecular defects in the genes for GPIbalpha GPIbbeta, and GPIX give rise to the Bernard-Soulier syndrome, in which thrombocytopenia and giant platelets suggest that this receptor also is involved in platelet production. To study how giant platelets are produced in vivo, we used a model of GPfbalpha-deficient mice (GPIbalpha(null)) and mice rescued with the human GPIbalpha transgene (GPIbalpha(null;Tg)). Materials and Methods. Using electron microscopy and immunogold labeling, we examined megakaryocytopoiesis in the bone marrow of these mice and developed a method to quantify the membranes of megakaryocytes (MK) and proplatelets by computer analysis. Results. Abnormal membrane development in the perinuclear zone was found in immature MK of GPIbalpha(null) mice. This led to a poorly developed demarcation membrane system and other ultrastructural changes. As a result, well-organized platelet territories were rarely seen within the cytoplasm of mature MK. Membrane quantification confirmed that MK of GPIbalpha(null) mice had a reduced internal membrane pool. Whereas these MK normally crossed the endothelial barrier, their migration was accompanied by the production of unusually large MK fragments or proplatelets in the vascular sinus with an approximately 50% decrease in internal membrane content compared to wild-type. In the rescued GPIbalpha(null;Tg) model, GPIbalpha was normally localized in MK, and there was a total correction of the ultrastructural defects. Conclusions. GPIba is essential for membrane development and distribution in maturing MK. Its absence leads to abnormal partitioning of the membrane systems and abnormal proplatelet production. (C) 2002 International Society for Experimental Hematology. Published by Elsevier Science Inc.
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页码:352 / 360
页数:9
相关论文
共 40 条
[1]   Binding of purified 14-3-3 ζ signaling protein to discrete amino acid sequences within the cytoplasmic domain of the platelet membrane glycoprotein Ib-IX-V complex [J].
Andrews, RK ;
Harris, SJ ;
McNally, T ;
Berndt, MC .
BIOCHEMISTRY, 1998, 37 (02) :638-647
[2]  
ANDREWS RK, 1992, J BIOL CHEM, V267, P18605
[3]   Structural and functional characterization of the mouse von Willebrand factor receptor GPIb-IX with novel monoclonal antibodies [J].
Bergmeier, W ;
Rackebrandt, K ;
Schröder, W ;
Zirngibl, H ;
Nieswandt, B .
BLOOD, 2000, 95 (03) :886-893
[4]   The cytoplasmic domain of the alpha-subunit of glycoprotein (GP) Ib mediates attachment of the entire GP Ib-IX complex to the cytoskeleton and regulates von Willebrand factor-induced changes in cell morphology [J].
Cunningham, JG ;
Meyer, SC ;
Fox, JEB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (19) :11581-11587
[5]  
DEBOTTON S, 2001, THROMB HAEMOST S
[6]   Identification of a finding sequence for the 14-3-3 protein within the cytoplasmic domain of the adhesion receptor, platelet glycoprotein Ib alpha [J].
Du, XP ;
Fox, JE ;
Pei, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (13) :7362-7367
[7]   Cytoplasmic domains of GpIbα and GpIbβ regulate 14-3-3ζ binding to GpIb/IX/V [J].
Feng, SJ ;
Christodoulides, N ;
Reséndiz, JC ;
Berndt, MC ;
Kroll, MH .
BLOOD, 2000, 95 (02) :551-557
[8]   Transendothelial migration of megakaryocytes in response to stromal cell-derived factor 1 (SDF-1) enhances platelet formation [J].
Hamada, T ;
Möhle, R ;
Hesselgesser, J ;
Hoxie, J ;
Nachman, RL ;
Moore, MAS ;
Rafii, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (03) :539-548
[9]   THE CYTOSKELETON OF THE RESTING HUMAN BLOOD-PLATELET - STRUCTURE OF THE MEMBRANE SKELETON AND ITS ATTACHMENT TO ACTIN-FILAMENTS [J].
HARTWIG, JH ;
DESISTO, M .
JOURNAL OF CELL BIOLOGY, 1991, 112 (03) :407-425
[10]   STUDIES ON THE MEGAKARYOCYTES OF A PATIENT WITH THE BERNARD-SOULIER SYNDROME [J].
HOURDILLE, P ;
PICO, M ;
JANDROTPERRUS, M ;
LACAZE, D ;
LOZANO, M ;
NURDEN, AT .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 76 (04) :521-530