Regulation of megakaryocytopoiesis and platelet production by tyrosine kinases and tyrosine phosphatases

被引:16
作者
Avraham, H [1 ]
Price, DJ [1 ]
机构
[1] Harvard Univ, Inst Med, Beth Israel Deaconess Med Ctr, Div Expt Med, Boston, MA 02115 USA
来源
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY | 1999年 / 17卷 / 03期
关键词
D O I
10.1006/meth.1998.0735
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Megakaryocytopoiesis is the process by which bone marrow progenitor cells develop into mature megakaryocytes, which in turn produce platelets required for normal hemostasis. The development of this hematopoietic lineage depends on a variety of growth factors and cytokines, Growth factor-dependent tyrosine kinase receptors important in megakaryocytopoiesis include c-Kit, fibroblast growth factor receptor, the RON receptor, and the macrophage colony-stimulating factor receptor, Binding of growth factors to their respective receptors results in receptor dimerization and subsequent autophosphorylation on tyrosine residues. Tyrosine autophosphorylations become sites of association for cytoplasmic signaling molecules via their SH2 domains. Some of these molecules are themselves cytoplasmic tyrosine kinases such as the Src kinases, TEC, and CHK. Others are molecules such as phospholipase C-gamma, phosphoinositol 3-kinase, Shc, GTPase-activating protein, and the SH2-containing tyrosine phosphatases SHP-1 and SHP-2, These molecules generate second messengers, regulate the phosphorylation of other downstream molecules, and also regulate the phosphorylation of the receptor itself, The different cytoplasmic components activate pathways involved in either changes in cell growth or changes in the cytoskeleton that affect maturation of the cell. Cytokine receptors also generate signals involved in growth and differentiation. Some of these second messengers overlap with those of the receptor tyrosine kinases, Others, such as the JAKs/STATs, are involved in transcriptional control and are unique to the signaling mediated by cytokine receptors, We describe the contribution of these different signals to the growth/differentiation processes of megakaryocytes. We also describe the contribution of receptor and nonreceptor tyrosine phosphatases to these processes. Lastly, we have compiled selected methods related to the study of protein phosphorylation in megakaryocytes. (C) 1999 Academic Press.
引用
收藏
页码:250 / 264
页数:15
相关论文
共 126 条
  • [21] CHOW LML, 1994, ONCOGENE, V9, P3437
  • [22] NTK - A CSK-RELATED PROTEIN-TYROSINE KINASE EXPRESSED IN BRAIN AND T-LYMPHOCYTES
    CHOW, LML
    JARVIS, C
    HU, QL
    NYE, SH
    GERVAIS, FG
    VEILLETTE, A
    MATIS, LA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) : 4975 - 4979
  • [23] ACTIVATION OF SRC FAMILY KINASES BY COLONY STIMULATING FACTOR-I, AND THEIR ASSOCIATION WITH ITS RECEPTOR
    COURTNEIDGE, SA
    DHAND, R
    PILAT, D
    TWAMLEY, GM
    WATERFIELD, MD
    ROUSSEL, MF
    [J]. EMBO JOURNAL, 1993, 12 (03) : 943 - 950
  • [24] Chk, a Csk family tyrosine protein kinase, exhibits Csk-like activity in fibroblasts, but not in an antigen-specific T-cell line
    Davidson, D
    Chow, LML
    Veillette, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (02) : 1355 - 1362
  • [25] CLONING AND EXPRESSION OF 2 DISTINCT HIGH-AFFINITY RECEPTORS CROSS-REACTING WITH ACIDIC AND BASIC FIBROBLAST GROWTH-FACTORS
    DIONNE, CA
    CRUMLEY, G
    BELLOT, F
    KAPLOW, JM
    SEARFOSS, G
    RUTA, M
    BURGESS, WH
    JAYE, M
    SCHLESSINGER, J
    [J]. EMBO JOURNAL, 1990, 9 (09) : 2685 - 2692
  • [26] Cloning and characterization of fetal liver phosphatase 1, a nuclear protein tyrosine phosphatase isolated from hematopoietic stem cells
    Dosil, M
    Leibman, N
    Lemischka, IR
    [J]. BLOOD, 1996, 88 (12) : 4510 - 4525
  • [27] THE W-SH AND PH MUTATIONS AFFECT THE C-KIT EXPRESSION PROFILE - C-KIT MISEXPRESSION IN EMBRYOGENESIS IMPAIRS MELANOGENESIS IN W-SH AND PH MUTANT MICE
    DUTTLINGER, R
    MANOVA, K
    BERROZPE, G
    CHU, TY
    DELEON, V
    TIMOKHINA, I
    CHAGANTI, RSK
    ZELENETZ, AD
    BACHVAROVA, RF
    BESMER, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) : 3754 - 3758
  • [28] PURE HUMAN HEMATOPOIETIC PROGENITORS - PERMISSIVE ACTION OF BASIC FIBROBLAST GROWTH-FACTOR
    GABBIANELLI, M
    SARGIACOMO, M
    PELOSI, E
    TESTA, U
    ISACCHI, G
    PESCHLE, C
    [J]. SCIENCE, 1990, 249 (4976) : 1561 - 1564
  • [29] BASIC FIBROBLAST GROWTH-FACTOR (B-FGF) INDUCES EARLY-STAGE (CFU-S) AND LATE-STAGE HEMATOPOIETIC PROGENITOR-CELL COLONY FORMATION (CFU-GM, CFU-MEG, AND BFU-E) BY SYNERGIZING WITH GM-CSF, MEG-CSF, AND ERYTHROPOIETIN, AND IS A RADIOPROTECTIVE AGENT INVITRO
    GALLICCHIO, VS
    HUGHES, NK
    HULETTE, BC
    DELLAPUCA, R
    NOBLITT, L
    [J]. INTERNATIONAL JOURNAL OF CELL CLONING, 1991, 9 (03): : 220 - 232
  • [30] GRABAREK J, 1994, J BIOL CHEM, V269, P21718