Serine protease inhibitors serpina1 and serpina3 are down-regulated in bone marrow during hematopoietic progenitor mobilization

被引:88
作者
Winkler, IG
Hendy, J
Coughlin, P
Horvath, A
Lévesque, JP
机构
[1] Mater Med Res Inst, Haematopoiet Stem Cell Lab, Brisbane, Qld 4101, Australia
[2] Peter MacCallum Canc Ctr, Melbourne, Vic 3002, Australia
[3] Monash Univ, Box Hill Hosp, Dept Med, Box Hill, Vic 3128, Australia
基金
英国惠康基金;
关键词
D O I
10.1084/jem.20042299
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mobilization of hematopoietic progenitor cells into the blood involves a massive release of neutrophil serine proteases in the bone marrow. We hypothesize that the activity of these neutrophil serine proteases is regulated by the expression of naturally occurring inhibitors (serpina1 and serpina3) produced locally within the bone marrow. We found that serpina1 and serpina3 were transcribed in the bone marrow by many different hematopoietic cell populations and that a strong reduction in expression occurred both at the protein and mRNA levels during mobilization induced by granulocyte colony-stimulating factor or chemotherapy. This decreased expression was restricted to the bone marrow as serpina1 expression was maintained in the liver, leading to no change in plasma concentrations during mobilization. The down-regulation of serpina1 and serpina3 during mobilization may contribute to a shift in the balance between serine proteases and their inhibitors, and an accumulation of active neutrophil serine proteases in bone marrow extravascular fluids that cleave and inactivate molecules essential to the retention of hematopoietic progenitor cells within the bone marrow. These data suggest an unexpected role for serpina1 and serpina3 in regulating the bone marrow hematopoietic microenvironment as well as influencing the migratory behavior of hematopoietic precursors.
引用
收藏
页码:1077 / 1088
页数:12
相关论文
共 48 条
[1]   SEQUENTIAL CHANGES OF PLASMA-PROTEINS AFTER SURGICAL TRAUMA [J].
ARONSEN, KF ;
KINDMARK, CO ;
LAURELL, CB ;
EKELUND, G .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1972, 29 :127-&
[2]   Functional diversification during evolution of the murine α1-proteinase inhibitor family:: Role of the hypervariable reactive center loop [J].
Barbour, KW ;
Goodwin, RL ;
Guillonneau, F ;
Wang, YP ;
Baumann, H ;
Berger, FG .
MOLECULAR BIOLOGY AND EVOLUTION, 2002, 19 (05) :718-727
[3]   MOUSE ALPHA-1-PROTEASE INHIBITOR IS NOT AN ACUTE PHASE REACTANT [J].
BAUMANN, H ;
LATIMER, JJ ;
GLIBETIC, MD .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 246 (01) :488-493
[4]  
BEATTY K, 1980, J BIOL CHEM, V255, P3931
[5]   Development of neutrophil granule diversity [J].
Borregaard, N .
PHAGOCYTES: BIOLOGY, PHYSIOLOGY, PATHOLOGY, AND PHARMACOTHERAPEUTICS, 1997, 832 :62-68
[6]   Granules of the human neutrophilic polymorphonuclear leukocyte [J].
Borregaard, N ;
Cowland, JB .
BLOOD, 1997, 89 (10) :3503-3521
[7]   MULTIPLE MURINE ALPHA-1-PROTEASE INHIBITOR GENES SHOW UNUSUAL EVOLUTIONARY DIVERGENCE [J].
BORRIELLO, F ;
KRAUTER, KS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9417-9421
[8]   The individual regulation of granule protein mRNA levels during neutrophil maturation explains the heterogeneity of neutrophil granules [J].
Cowland, JB ;
Borregaard, N .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (06) :989-995
[9]   Efficient mobilization of haematopoietic progenitors after a single injection of pegylated recombinant human granulocyte colony-stimulating factor in mouse strains with distinct marrow-cell pool sizes [J].
de Haan, G ;
Ausema, A ;
Wilkens, M ;
Molineux, G ;
Dontje, B .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 110 (03) :638-646
[10]   GRANULOCYTE-COLONY-STIMULATING FACTOR ADMINISTRATION TO HEALTHY-VOLUNTEERS - ANALYSIS OF THE IMMEDIATE ACTIVATING EFFECTS ON CIRCULATING NEUTROPHILS [J].
DEHAAS, M ;
KERST, JM ;
VANDERSCHOOT, CE ;
CALAFAT, J ;
HACK, CE ;
NUIJENS, JH ;
ROOS, D ;
VANOERS, RHJ ;
VONDEMBORNE, AEGK .
BLOOD, 1994, 84 (11) :3885-3894