Nitric oxide induces apoptosis in megakaryocytic cell lines

被引:56
作者
Battinelli, E
Loscalzo, J
机构
[1] Boston Univ, Sch Med, Evans Dept Med, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Whitaker Cardiovasc Inst, Boston, MA 02118 USA
关键词
D O I
10.1182/blood.V95.11.3451.011k34_3451_3459
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytokines that stimulate inducible nitric oxide (NO) synthase can suppress the growth and differentiation of normal human bone marrow cells, including megakaryocytes, Since NO promotes apoptosis in other cell systems, we chose to study the determinants of apoptosis in megakaryocytic cells. We show that both exogenous and endogenous sources of NO can induce apoptosis in megakaryocytoid cell lines. The megakaryocyte growth factor thrombopoietin suppresses NO-induced apoptosis, whereas treatment with peroxynitrite, a cytotoxic product formed when NO reacts with superoxide, promotes apoptosis, Superoxide inhibitors suppress NO-induced apoptosis, and pretreatment with megakaryocyte growth and maturation factors attenuates NO-induced apoptosis, These data show that NO modulates megakaryocyte apoptosis and suggest that this process may occur in the cytokine-rich marrow milieu to regulate megakaryocyte turnover. (C) 2000 by The American Society of Hematology.
引用
收藏
页码:3451 / 3459
页数:9
相关论文
共 48 条
[1]  
ABO J, 1993, BLOOD, V82, P2829
[2]   Modulation of the mitochondrial permeability transition by nitric oxide [J].
Balakirev, MY ;
Khramtsov, VV ;
Zimmer, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 246 (03) :710-718
[3]  
Beckman JS, 1996, AM J PHYSIOL-CELL PH, V271, pC1424
[4]   Ability of early acting cytokines to directly promote survival and suppress apoptosis of human primitive CD34(+)CD38(-) bone marrow cells with multilineage potential at the single-cell level: Key role of thrombopoietin [J].
Borge, OJ ;
Ramsfjell, V ;
Cui, L ;
Jacobsen, SEW .
BLOOD, 1997, 90 (06) :2282-2292
[5]   Thrombopoietin, but not erythropoietin promotes viability and inhibits apoptosis of multipotent murine hematopoietic progenitor cells in vitro [J].
Borge, OJ ;
Ramsfjell, V ;
Veiby, OP ;
Murphy, MJ ;
Lok, S ;
Jacobsen, SEW .
BLOOD, 1996, 88 (08) :2859-2870
[6]   U937 apoptotic cell death by nitric oxide:: Bcl-2 downregulation and caspase activation [J].
Brockhaus, F ;
Brüne, B .
EXPERIMENTAL CELL RESEARCH, 1998, 238 (01) :33-41
[7]   Nitric oxide inhibition of cytochrome oxidase and mitochondrial respiration: Implications for inflammatory, neurodegenerative and ischaemic pathologies [J].
Brown, GC .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1997, 174 (1-2) :189-192
[8]  
DIMMELER S, 1992, J BIOL CHEM, V267, P16771
[9]   Interplay between NO and [Fe-S] clusters: Relevance to biological systems [J].
Drapier, JC .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1997, 11 (03) :319-329
[10]  
Drénou B, 1999, J IMMUNOL, V163, P4115