Literature DB >> 6753391

Cellular changes in bone marrow of malaria-infected mice. III. Chemotaxis of granulocytes.

S Frankenburg, M V Londner, C L Greenblatt.   

Abstract

The number of bone marrow cells and their chemotactic activity was studied during malaria infection. Two days after infection of Balb/c mice with Plasmodium berghei, an increase in granulocyte number was observed in the blood. A modified Boyden chamber chemotaxis assay was employed to investigate the mechanism of granulocyte accumulation in the blood. Bone marrow cells from normal mice, from mice during a primary lethal infection and from immune mice after challenge were compared. The complement factor C5a showed chemotactic activity for bone marrow cells; a significant decrease of chemotaxis was only observed after 6 days of primary infection. Extracts of spleen, liver and infected erythrocytes lacked chemotactic activity, or caused inhibition of cell migration. Serum from mice with a 2-day primary infection contained chemotactic activity. The active component was heat labile, protease sensitive and had an estimated molecular weight of 250,000.

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Year:  1982        PMID: 6753391     DOI: 10.1007/bf00926656

Source DB:  PubMed          Journal:  Z Parasitenkd        ISSN: 0044-3255


  15 in total

1.  Evaluation of marrow granulocytic reserves in normal and disease states.

Authors:  C G CRADDOCK; S PERRY; L E VENTZKE; J S LAWRENCE
Journal:  Blood       Date:  1960-06       Impact factor: 22.113

2.  Studies of the neutropenia of acute malaria.

Authors:  D C Dale; S M Wolff
Journal:  Blood       Date:  1973-02       Impact factor: 22.113

3.  Tumor-associated eosinophilotactic factor.

Authors:  S I Wasserman; E J Goetzl; L Ellman; K F Austen
Journal:  N Engl J Med       Date:  1974-02-21       Impact factor: 91.245

4.  Human mononuclear leukocyte chemotaxis: a quantitative assay for humoral and cellular chemotactic factors.

Authors:  R Snyderman; L C Altman; M S Hausman; S E Mergenhagen
Journal:  J Immunol       Date:  1972-03       Impact factor: 5.422

5.  Complement-derived leukotactic factors in pathological fluids.

Authors:  P A Ward
Journal:  J Exp Med       Date:  1971-09-01       Impact factor: 14.307

6.  Controlling the production of blood cells.

Authors:  M J Cline; D W Golde
Journal:  Blood       Date:  1979-01       Impact factor: 22.113

7.  Spleen-derived mononuclear cell chemotactic factor in malaria infections: a possible mechanism for splenic macrophage accumulation.

Authors:  D J Wyler; J I Gallin
Journal:  J Immunol       Date:  1977-02       Impact factor: 5.422

8.  Cellular changes in the bone marrow of plasmodium berghei-infected mice. II. Blast transformation and phagocytosis.

Authors:  S Frankenburg; M V Londner; C L Greenblatt
Journal:  Cell Immunol       Date:  1980-09-15       Impact factor: 4.868

9.  Soluble antigens released in vitro from erythrocytes infected with Plasmodium berghei.

Authors:  H Weissberger; J Golenser; D T Spira
Journal:  Bull World Health Organ       Date:  1979       Impact factor: 9.408

10.  Biological activity of complement in vivo. Role of C5 in the accumulation of polymorphonuclear leukocytes in inflammatory exudates.

Authors:  R Snyderman; J K Phillips; S E Mergenhagen
Journal:  J Exp Med       Date:  1971-11-01       Impact factor: 14.307

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