Elevated levels of basic fibroblast growth factor in megakaryocytes and platelets from patients with idiopathic myelofibrosis

被引:113
作者
Martyre, MC
LeBousseKerdiles, MC
Romquin, N
Chevillard, S
Praloran, V
Demory, JL
Dupriez, B
机构
[1] HOP PAUL BROUSSE,INSERM,U268,VILLEJUIF,FRANCE
[2] CHRU,SERV HEMATOL,LIMOGES,FRANCE
[3] CHRU,SERV MALAD SANG,LILLE,FRANCE
[4] CTR HOSP ST VINCENT,LILLE,FRANCE
[5] CTR HOSP,HEMATOL CLIN,LENS,FRANCE
[6] INST CURIE,SECT RECH,INSERM,U365,F-75248 PARIS 05,FRANCE
[7] INST CURIE,LAB TRANSFERT,F-75248 PARIS,FRANCE
关键词
bFGF; megakaryocytes; platelets; idiopathic myelofibrosis;
D O I
10.1046/j.1365-2141.1997.292671.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Idiopathic myelofibrosis, or agnogenic myeloid metaplasia, is a chronic myeloproliferative disorder characterized by clonal expansion and marrow fibrosis. Although marrow fibrosis appears to be a reactive process, it substantially contributes to impaired haemopoiesis. During the last few years the implication of megakaryocyte-derived growth factors in its pathogenesis has been documented. We previously reported increased expression of TGF-beta in patients with idiopathic myelofibrosis. In the present study we show that circulating megakaryocytic cells from such patients expressed high levels of basic fibroblast growth factor (bFGF). An increased expression of bFGF was also detected in patients' platelets. Under culture conditions, bFGF present in megakaryocytic cells was not exported into the medium, consistent with the fact that bFGF is devoid of a secretion peptide signal. Interestingly, this lack of bFGF secretion was observed in all patients but one, who was in an accelerated phase of the disease and presented an important percentage of circulating megakaryoblasts.
引用
收藏
页码:441 / 448
页数:8
相关论文
共 33 条
  • [21] TGF-beta and megakaryocytes in the pathogenesis of myelofibrosis in myeloproliferative disorders
    Martyre, MC
    [J]. LEUKEMIA & LYMPHOMA, 1995, 20 (1-2) : 39 - &
  • [22] Elevated intracellular level of basic fibroblast growth factor correlates with stage of chronic lymphocytic leukemia and is associated with resistance to fludarabine
    Menzel, T
    Rahman, Z
    Calleja, E
    White, K
    Wilson, EL
    Wieder, R
    Gabrilove, J
    [J]. BLOOD, 1996, 87 (03) : 1056 - 1063
  • [23] RELEASE OF BASIC FIBROBLAST GROWTH-FACTOR, AN ANGIOGENIC FACTOR DEVOID OF SECRETORY SIGNAL SEQUENCE - A TRIVIAL PHENOMENON OR A NOVEL SECRETION MECHANISM
    MIGNATTI, P
    RIFKIN, DB
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1991, 47 (03) : 201 - 207
  • [24] METABOLISM OF RECEPTOR-BOUND AND MATRIX-BOUND BASIC FIBROBLAST GROWTH-FACTOR BY BOVINE CAPILLARY ENDOTHELIAL-CELLS
    MOSCATELLI, D
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 107 (02) : 753 - 759
  • [25] Long-Term Culture of Human Bone Marrow Stromal Cells in the Presence of Basic Fibroblast Growth Factor
    Oliver, Lisa J.
    Rifkin, Daniel B.
    Gabrilove, Janice
    Hannocks, Melanie-Jane
    Wilson, E. Lynette
    [J]. GROWTH FACTORS, 1990, 3 (03) : 231 - 236
  • [26] CHARACTERIZATION OF AN ACUTE MICROMEGAKARYOCYTIC LEUKEMIA - EVIDENCE FOR THE PATHOGENESIS OF MYELOFIBROSIS
    REILLY, JT
    BARNETT, D
    DOLAN, G
    FORREST, P
    EASTHAM, J
    SMITH, A
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1993, 83 (01) : 58 - 62
  • [27] CIRCULATING HUMAN-BLOOD PLATELETS RETAIN APPRECIABLE AMOUNTS OF POLY(A)+ RNA
    ROTH, GJ
    HICKEY, MJ
    CHUNG, DW
    HICKSTEIN, DD
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 160 (02) : 705 - 710
  • [28] A NOVEL SECRETORY PATHWAY FOR INTERLEUKIN-1-BETA, A PROTEIN LACKING A SIGNAL SEQUENCE
    RUBARTELLI, A
    COZZOLINO, F
    TALIO, M
    SITIA, R
    [J]. EMBO JOURNAL, 1990, 9 (05) : 1503 - 1510
  • [29] THIELE J, 1991, J SUBMICR CYTOL PATH, V23, P93
  • [30] GROWTH INHIBITOR FROM BSC-1 CELLS CLOSELY RELATED TO PLATELET TYPE-BETA TRANSFORMING GROWTH-FACTOR
    TUCKER, RF
    SHIPLEY, GD
    MOSES, HL
    HOLLEY, RW
    [J]. SCIENCE, 1984, 226 (4675) : 705 - 707