Granulocyte Chemotaxis in the Chediak-Higashi Syndrome of Mink

Author:

Clark Robert A.12,Kimball Harry A.13,Padgett George A.14

Affiliation:

1. Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md., and Department of Veterinary Pathology, College of Veterinary Medicine, Washington State University, Pullman, Wash.

2. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.

3. Inflammatory Diseases Section, Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.

4. Washington State University, Pullman, Wash.

Abstract

Abstract Studies of granulocyte chemotaxis were performed in mink with the Chediak-Higashi syndrome. In vivo migration of leukocytes to an inflammatory site was reduced in the affected animals. In vitro studies documented a consistent early impairment in the chemotactic response of Chediak-Higashi mink granulocytes. Serum from Chediak-Higashi mink generated normal amounts of chemotactic factors. The cellular defect in leukocyte chemotaxis in mink is comparable to that observed in humans with the Chediak-Higashi syndrome and may contribute to the increased susceptibility to infection in this disease.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Carnivores;Comparative Hemostasis in Vertebrates;1996

2. Defective in vitro motility of polymorphonuclear leukocytes of homozygote and heterozygote Chediak-Higashi cats;Veterinary Immunology and Immunopathology;1992-03

3. Das Chédiak-Higashi-Syndrom;Ergebnisse der Inneren Medizin und Kinderheilkunde/Advances in Internal Medicine and Pediatrics;1992

4. Normal-Sized Primary Lysosomes Are Present in Chediak-Higashi Syndrome Neutrophils;Pediatric Research;1987-08

5. Millipore diffusion chambers allow dissociation of myelin phagocytosis by non-resident cells and of allogenic nerve graft rejection;Journal of the Neurological Sciences;1985-07

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