Concentrations of thrombopoietin in bone marrow in normal subjects and in patients with idiopathic thrombocytopenic purpura, aplastic anemia, and essential thrombocythemia correlate with its mRNA expression of bone marrow stromal cells

被引:84
作者
Hirayama, Y
Sakamaki, S
Matsunaga, T
Kuga, T
Kuroda, H
Kusakabe, T
Sasaki, K
Fujikawa, K
Kato, J
Kogawa, K
Koyama, R
Niitsu, Y
机构
[1] Sapporo Med Univ, Sch Med, Dept Internal Med 4, Chuo Ku, Sapporo, Hokkaido 0600061, Japan
[2] Hokkaido Prefectural Sapporo Kitano Hosp, Sapporo, Hokkaido, Japan
关键词
D O I
10.1182/blood.V92.1.46.413k44_46_52
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The function of bone marrow (BM) stromal thrombopoietin (TPO) in megakaryopoiesis remains unknown. In the present study we attempted to clarify the pathophysiological implications of stromal TPO in normal subjects (NS) and in patients with idiopathic thrombocytopenic purpura (ITP), aplastic anemia (AA), and essential thrombocythemia (ET) by measuring TPO concentrations in BM and peripheral blood (PB) and by estimating the levels of stromal TPO mRNA with TaqMan fluorescence-based post-reverse transcription-polymerase chain reaction product detection system. The results showed that TPO concentrations in PB were significantly elevated in patients with ITP (34.9 +/- 11.7 pg/mL) and AA (364.1 +/- 153.5 pg/mL) but within normal range in patients with ET (each 20.0 and 22.1; NS, 22.1 +/- 8.2 pg/mL). In all subjects, the TPO concentrations in BM correlated well with the PB levels, and the former were consistently higher than the latter. The concentrations of TPO in BM also correlated with the levels of TPO mRNA in stromal cells. Furthermore, expression levels of TPO mRNA clearly correlated with megakaryocyte counts in NS and patients with ITP, indicating that stromal TPO actually enhances megakaryopoiesis. Thus, our results in the present study indicate that TPO from BM stromal cells Is considered to play an essential role for megakaryopoiesis under various pathophysiological conditions. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:46 / 52
页数:7
相关论文
共 26 条
[1]   REGULATION OF PLATELET ACTIVATION IN-VITRO BY THE C-MPL LIGAND, THROMBOPOIETIN [J].
CHEN, JC ;
HERCEGHARJACEK, L ;
GROOPMAN, JE ;
GRABAREK, J .
BLOOD, 1995, 86 (11) :4054-4062
[2]  
DEBILI N, 1995, BLOOD, V86, P2516
[3]   STIMULATION OF MEGAKARYOCYTOPOIESIS AND THROMBOPOIESIS BY THE C-MPL LIGAND [J].
DESAUVAGE, FJ ;
HASS, PE ;
SPENCER, SD ;
MALLOY, BE ;
GURNEY, AL ;
SPENCER, SA ;
DARBONNE, WC ;
HENZEL, WJ ;
WONG, SC ;
KUANG, WJ ;
OLES, KJ ;
HULTGREN, B ;
SOLBERG, LA ;
GOEDDEL, DV ;
EATON, DL .
NATURE, 1994, 369 (6481) :533-538
[4]   CONDITIONS CONTROLLING PROLIFERATION OF HEMATOPOIETIC STEM-CELLS INVITRO [J].
DEXTER, TM ;
ALLEN, TD ;
LAJTHA, LG .
JOURNAL OF CELLULAR PHYSIOLOGY, 1977, 91 (03) :335-344
[5]  
Gelmini S, 1997, CLIN CHEM, V43, P752
[6]   A novel method for real time quantitative RT PCR [J].
Gibson, UEM ;
Heid, CA ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :995-1001
[7]   Thrombopoietin is synthesized by bone marrow stromal cells [J].
Guerriero, A ;
Worford, L ;
Holland, HK ;
Guo, GR ;
Sheehan, K ;
Waller, EK .
BLOOD, 1997, 90 (09) :3444-3455
[8]   CYTOKINE MESSENGER-RNA EXPRESSION OF BONE-MARROW STROMAL CELLS FROM PATIENTS WITH APLASTIC-ANEMIA AND MYELODYSPLASTIC SYNDROME [J].
HIRAYAMA, Y ;
KOHGO, Y ;
MATSUNAGA, T ;
OHI, S ;
SAKAMAKI, S ;
NIITSU, Y .
BRITISH JOURNAL OF HAEMATOLOGY, 1993, 85 (04) :676-683
[9]   PROMOTION OF MEGAKARYOCYTE PROGENITOR EXPANSION AND DIFFERENTIATION BY THE C-MPL LIGAND THROMBOPOIETIN [J].
KAUSHANSKY, K ;
LOK, S ;
HOLLY, RD ;
BROUDY, VC ;
LIN, N ;
BAILEY, MC ;
FORSTROM, JW ;
BUDDLE, MM ;
OORT, PJ ;
HAGEN, FS ;
ROTH, GJ ;
PAPAYANNOPOULOU, T ;
FOSTER, DC .
NATURE, 1994, 369 (6481) :568-571
[10]  
KOHGO Y, 1994, INT J HEMATOL, V59, P177