Expression of the secondary granule proteins major basic protein 1 (MBP-1) and eosinophil peroxidase (EPX) is required for eosinophilopoiesis in mice

被引:61
作者
Doyle, Alfred D. [1 ]
Jacobsen, Elizabeth A. [1 ]
Ochkur, Sergei I. [1 ]
McGarry, Michael P. [1 ]
Shim, Kevin G. [1 ]
Nguyen, David T. C. [2 ]
Protheroe, Cheryl [1 ]
Colbert, Dana [2 ]
Kloeber, Jake [1 ]
Neely, Joseph [2 ]
Shim, Kelly P. [1 ]
Dyer, Kimberly D. [3 ]
Rosenberg, Helene F. [3 ]
Lee, James J. [1 ]
Lee, Nancy A. [2 ]
机构
[1] Mayo Clin Arizona, Dept Biochem & Mol Biol, Div Pulm Med, Scottsdale, AZ 85259 USA
[2] Mayo Clin Arizona, Dept Biochem & Mol Biol, Div Hematol Oncol, Scottsdale, AZ 85259 USA
[3] NIAID, Inflammat Immunobiol Sect, Lab Allerg Dis, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
SEVERE CONGENITAL NEUTROPENIA; MOLECULAR-CLONING; RIBONUCLEASE GENES; MOUSE EOSINOPHILS; CATIONIC PROTEIN; IDENTIFICATION; LEADS; DEGRANULATION; INFLAMMATION; SUBGROUP;
D O I
10.1182/blood-2013-01-473405
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Eosinophil activities are often linked with allergic diseases such as asthma and the pathologies accompanying helminth infection. These activities have been hypothesized to be mediated, in part, by the release of cationic proteins stored in the secondary granules of these granulocytes. The majority of the proteins stored in these secondary granules (by mass) are major basic protein 1 (MBP-1) and eosinophil peroxidase (EPX). Unpredictably, a knockout approach targeting the genes encoding these proteins demonstrated that, unlike in mice containing a single deficiency of only MBP-1 or EPX, the absence of both granule proteins resulted in the near complete loss of peripheral blood eosinophils with no apparent impact on any other hematopoietic lineage. Moreover, the absence of MBP-1 and EPX promoted a concomitant loss of eosinophil lineage-committed progenitors in the marrow, identifying a specific blockade in eosinophilopoiesis as the causative event. Significantly, this blockade of eosinophilopoiesis is also observed in ex vivo cultures of marrow progenitors and is not rescued in vivo by adoptive bone marrow engraftment, suggesting a cell-autonomous defect in marrow progenitors. These observations implicate a role for granule protein gene expression as a regulator of eosinophilopoiesis and provide another strain of mice congenitally deficient of eosinophils.
引用
收藏
页码:781 / 790
页数:10
相关论文
共 47 条
[1]  
ACKERMAN SJ, 1983, J IMMUNOL, V131, P2977
[2]   ACIDIC POLYAMINO ACIDS INHIBIT HUMAN EOSINOPHIL GRANULE MAJOR BASIC-PROTEIN TOXICITY - EVIDENCE OF A FUNCTIONAL-ROLE FOR PROMBP [J].
BARKER, RL ;
GUNDEL, RH ;
GLEICH, GJ ;
CHECKEL, JL ;
LOEGERING, DA ;
PEASE, LR ;
HAMANN, KJ .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (03) :798-805
[3]  
BUTTERFIELD JH, 1984, EXP HEMATOL, V12, P163
[4]   Mouse eosinophil-associated ribonucleases: a unique subfamily expressed during hematopoiesis [J].
Cormier, SA ;
Larson, KA ;
Yuan, SB ;
Mitchell, TL ;
Lindenberger, K ;
Carrigan, P ;
Lee, NA ;
Lee, JJ .
MAMMALIAN GENOME, 2001, 12 (05) :352-361
[5]   TH2-mediated pulmonary inflammation leads to the differential expression of ribonuclease genes by alveolar macrophages [J].
Cormier, SA ;
Yuan, SB ;
Crosby, JR ;
Protheroe, CA ;
Dimina, DM ;
Hines, EM ;
Lee, NA ;
Lee, JJ .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 27 (06) :678-687
[6]   Eosinophil differentiation in the bone marrow is inhibited by T cell-derived IFN-γ [J].
de Bruin, Alexander M. ;
Buitenhuis, Miranda ;
van der Sluijs, Koenraad F. ;
van Gisbergen, Klaas P. J. M. ;
Boon, Louis ;
Nolte, Martijn A. .
BLOOD, 2010, 116 (14) :2559-2569
[7]   Eosinophil major basic protein-1 does not contribute to allergen-induced airway pathologies in mouse models of asthma [J].
Denzler, KL ;
Farmer, SC ;
Crosby, JR ;
Borchers, M ;
Cieslewicz, G ;
Larson, KA ;
Cormier-Regard, S ;
Lee, NA ;
Lee, JJ .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5509-5517
[8]   Extensive eosinophil degranulation and peroxidase-mediated oxidation of airway proteins do not occur in a mouse ovalbumin-challenge model of pulmonary inflammation [J].
Denzler, KL ;
Borchers, MT ;
Crosby, JR ;
Cieslewicz, G ;
Hines, EM ;
Justice, JP ;
Cormier, SA ;
Lindenberger, KA ;
Song, W ;
Wu, WJ ;
Hazen, SL ;
Gleich, GJ ;
Lee, JJ ;
Lee, NA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1672-1682
[9]   Congenital neutropenia: diagnosis, molecular bases and patient management [J].
Donadieu, Jean ;
Fenneteau, Odile ;
Beaupain, Blandine ;
Mahlaoui, Nizar ;
Chantelot, Christine Bellanne .
ORPHANET JOURNAL OF RARE DISEASES, 2011, 6
[10]   Homologous recombination into the eosinophil peroxidase locus generates a strain of mice expressing Cre recombinase exclusively in eosinophils [J].
Doyle, Alfred D. ;
Jacobsen, Elizabeth A. ;
Ochkur, Sergei I. ;
Willetts, Lian ;
Shim, Kelly ;
Neely, Joseph ;
Kloeber, Jake ;
LeSuer, Will E. ;
Pero, Ralph S. ;
Lacy, Paige ;
Moqbel, Redwan ;
Lee, Nancy A. ;
Lee, James J. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2013, 94 (01) :17-24