Literature DB >> 686156

The Chédiak-Higashi syndrome. Evidence that defective leukotaxis is primarily due to an impediment by giant granules.

C C Clawson, J G White, J E Repine.   

Abstract

The primary defect of the Chédiak-Higashi syndrome (CHS) which links the several known neutrophil abnormalities in this disorder remains enigmatic. In an attempt to clarify the mechanism of one of the abnormalities of CHS neutrophils, ie, chemotactic migration, the effect of filter pore size was examined in the standard Boyden chamber assay. The response of normal neutrophils to a gradient of zymosan-activated serum was not influenced by increasing the filter pore size from 5 to 8 microgram. However, while CHS neutrophils showed a significant reduction in migratory response from the controls with 5-mu filters, the difference was eliminated when 8-mu filters were employed. Again, when an arachidonic acid gradient was used as the stimulus, migration of CHS neutrophils through 8-mu filters equalled that of controls. These findings indicate the intact nature of the surface receptor and motility systems of the CHS neutrophils and further suggest that the previously defined chemotactic defect in these cells can be explained in terms of the mechanical impediment provided by the CHS giant cytoplasmic granules.

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Year:  1978        PMID: 686156      PMCID: PMC2018262     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  17 in total

1.  Granulocyte function in the Chediak-Higashi syndrome of mice.

Authors:  J I Gallin; J S Bujak; E Patten; S M Wolff
Journal:  Blood       Date:  1974-02       Impact factor: 22.113

2.  The Chediak-Higashi syndrome: studies of host defenses.

Authors:  S M Wolff
Journal:  Ann Intern Med       Date:  1972-02       Impact factor: 25.391

3.  Granulocyte chemotaxis in the Chediak-Higashi syndrome of mink.

Authors:  R A Clark; H R Kimball; G A Padgett
Journal:  Blood       Date:  1972-05       Impact factor: 22.113

4.  Defective mononuclear leukocyte chemotaxis in the Chediak-Higashi syndrome of humans, mink, and cattle.

Authors:  J I Gallin; J A Klimerman; G A Padgett; S M Wolff
Journal:  Blood       Date:  1975-06       Impact factor: 22.113

5.  Giant organelles containing tubules in Chediak-Higashi lymphocytes.

Authors:  J G White
Journal:  Am J Pathol       Date:  1972-11       Impact factor: 4.307

6.  Abnormal bactericidal, metabolic, and lysosomal functions of Chediak-Higashi Syndrome leukocytes.

Authors:  R K Root; A S Rosenthal; D J Balestra
Journal:  J Clin Invest       Date:  1972-03       Impact factor: 14.808

7.  Enhancement of random migration and chemotactic response of human leukocytes by ascorbic acid.

Authors:  E J Goetzl; S I Wasserman; I Gigli; K F Austen
Journal:  J Clin Invest       Date:  1974-03       Impact factor: 14.808

Review 8.  Impaired microtubule function correctable by cyclic GMP and cholinergic agonists in the Chediak-Higashi syndrome.

Authors:  J M Oliver
Journal:  Am J Pathol       Date:  1976-11       Impact factor: 4.307

9.  Improvement of Chediak-Higashi leukocyte function by cyclic guanosine monophosphate.

Authors:  L A Boxer; M Rister; J M Allen; R L Baehner
Journal:  Blood       Date:  1977-01       Impact factor: 22.113

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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  11 in total

1.  Immunological studies of NK cell-deficient beige mice. II. Analysis of T-lymphocyte functions in beige mice.

Authors:  M E Baca; A M Mowat; D M Parrott
Journal:  Immunology       Date:  1989-01       Impact factor: 7.397

2.  Chédiak-Higashi syndrome neutrophils are characterized by the absence of both normal azurophilic granules.

Authors:  B C West
Journal:  Am J Pathol       Date:  1986-01       Impact factor: 4.307

3.  Enlarged dysmorphic lysosomes in an established beige (C57BL/6J;bgJ(/bgJ)) mouse mutant fibroblast line: a reversible characteristic.

Authors:  J B Gow; T A Lyerla; S Lainwala
Journal:  In Vitro Cell Dev Biol Anim       Date:  1996-09       Impact factor: 2.416

4.  Cellular expression of the beige mouse mutation and its correction in hybrids with control human fibroblasts.

Authors:  J B Gow; S Lainwala; T A Lyerla
Journal:  In Vitro Cell Dev Biol Anim       Date:  1993-11       Impact factor: 2.416

5.  Immunological studies of NK cell-deficient beige mice. I. Defective ability of beige lymphocytes to mediate local and systemic graft-versus-host reactions.

Authors:  M E Baca; A M Mowat
Journal:  Immunology       Date:  1989-01       Impact factor: 7.397

Review 6.  Genetic defects in Chediak-Higashi syndrome and the beige mouse.

Authors:  R A Spritz
Journal:  J Clin Immunol       Date:  1998-03       Impact factor: 8.317

Review 7.  Neutrophil homeostasis and periodontal health in children and adults.

Authors:  E Hajishengallis; G Hajishengallis
Journal:  J Dent Res       Date:  2013-10-04       Impact factor: 6.116

8.  The Chédiak-Higashi syndrome; the nature of the giant neutrophil granules and their interactions with cytoplasm and foreign particulates. I. Progressive enlargement of the massive inclusions in mature neutrophils. II. Manifestations of cytoplasmic injury and sequestration. III. Interactions between giant organelles and foreign particulates.

Authors:  J G White; C C Clawson
Journal:  Am J Pathol       Date:  1980-01       Impact factor: 4.307

9.  Mast cell degranulation in beige mice with the Chédiak-Higashi defect.

Authors:  K C Poon; P I Liu; S S Spicer
Journal:  Am J Pathol       Date:  1981-08       Impact factor: 4.307

10.  The Chédiak-Higashi syndrome: ring-shaped lysomomes in circulating monocytes.

Authors:  J G White; C C Clawson
Journal:  Am J Pathol       Date:  1979-09       Impact factor: 4.307

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