Literature DB >> 3681189

Elastase and cathepsin G activities are present in immature bone marrow neutrophils and absent in late marrow and circulating neutrophils of beige (Chediak-Higashi) mice.

K H Takeuchi1, M P McGarry, R T Swank.   

Abstract

Elicited peritoneal neutrophils of beige (Chediak-Higashi) mice essentially lack activities of the neutral serine proteinases elastase and cathepsin G, which may explain the increased susceptibility to infection of beige mice and Chediak-Higashi patients. We have examined neutrophils of beige mice at earlier points in their development to determine if the proteinase genes are never expressed or whether they are expressed and then lost during neutrophil maturation. Surprisingly, bone marrow of beige mice had significant elastase and cathepsin G activity (approximately 60% of normal). The results of several experiments indicate that neutrophils were the sole source of elastase and cathepsin G in bone marrow. Neutral proteinase activity was readily demonstrable by histochemical procedures in beige marrow neutrophil precursors up to and including the metamyelocyte stage. However, mature neutrophils of beige marrow had greatly decreased activity. Also mature neutrophils (PMNs) of the peripheral circulation, like peritoneal neutrophils, had very low elastase and cathepsin C activities. Thus we conclude that beige neutrophil precursors express neutral proteinase activity, which is largely and irreversibly depleted by the time they fully mature in marrow.

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Year:  1987        PMID: 3681189      PMCID: PMC2189659          DOI: 10.1084/jem.166.5.1362

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  26 in total

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Journal:  Biochim Biophys Acta       Date:  1977-11-23

3.  Metallic copper-induced granulocyte exudation in the study of granulocytopoiesis.

Authors:  M P McGarry
Journal:  Cell Tissue Kinet       Date:  1975-07

4.  Elastases from human and canine granulocytes, II. Interaction with protease inhibitors of animal, plant, and microbial origin.

Authors:  H Schiessler; K Ohlsson; I Olsson; M Arnhold; Y Birk; H Fritz
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1977-01

5.  The effect of human granulocyte elastase on bacterial suspensions.

Authors:  A Janoff; J Blondin
Journal:  Lab Invest       Date:  1973-10       Impact factor: 5.662

6.  The Chediak-Higashi syndrome: cytoplasmic sequestration in circulating leukocytes.

Authors:  J G White
Journal:  Blood       Date:  1967-04       Impact factor: 22.113

7.  Serotonin deficiency and prolonged bleeding in beige mice.

Authors:  J M Holland
Journal:  Proc Soc Exp Biol Med       Date:  1976-01

8.  The Chediak-Higashi syndrome of cats.

Authors:  J W Kramer; W C Davis; D J Prieur
Journal:  Lab Invest       Date:  1977-05       Impact factor: 5.662

9.  Formation of anomalous lysosomes in monocytes, neutrophils, and eosinophils from bone marrow of mice with Chédiak-Higashi syndrome.

Authors:  C Oliver; E Essner
Journal:  Lab Invest       Date:  1975-01       Impact factor: 5.662

10.  Correction of leukocyte function in Chediak-Higashi syndrome by ascorbate.

Authors:  L A Boxer; A M Watanabe; M Rister; H R Besch; J Allen; R L Baehner
Journal:  N Engl J Med       Date:  1976-11-04       Impact factor: 91.245

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  5 in total

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Authors:  R Pettipher; J Edwards; S Cruwys; E Jessup; J Beesley; B Henderson
Journal:  Am J Pathol       Date:  1990-11       Impact factor: 4.307

3.  Neutrophil elastase and cathepsin G protein and messenger RNA expression in bone marrow from a patient with Chediak-Higashi syndrome.

Authors:  D Burnett; C J Ward; R A Stockley; R G Dalton; A J Cant; S Hoare; J Crocker
Journal:  Clin Mol Pathol       Date:  1995-02

4.  Neutrophil function in children following allogeneic hematopoietic stem cell transplant.

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Journal:  Pediatr Transplant       Date:  2016-04-25

5.  Inflammation and the reciprocal production of granulocytes and lymphocytes in bone marrow.

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  5 in total

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