Abstract
The number of bone marrow cells and their chemotactic activity was studied during malaria infection. Two days after infection of Balb/c mice withPlasmodium 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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References
Athens JW (1970) Neutrophilic granulocyte kinetics and granulocytopoiesis. In: Gordon AS (ed) Regulation of Hematopoiesis. Appleton Century-Crofts, New York, 2:1143–1166
Cline MJ, Golde DW (1979) Controlling the production of red cells. Blood 53:157–165
Craddock CG Jr, Perry S, Veutzke LE, Lawrence JS (1960) Evaluation of marrow granulocyte reserves in normal and disease states. Blood 15:840–855
Dale DC, Wolff SM (1973) Studies of the neutropenia of acute malaria. Blood 41:197–206
De Chatelet LR (1979) Phagocytosis by human neutrophils. In: Gadebusch HH (ed) Phagocytes and cellular immunity. CRC Press, Inc, pp 1–56
Frankenburg S, Greenblatt CL (1978) Cellular changes in the bone marrow ofPlasmodium berghei-infected mice. Isr J Med Sci 14:582–589
Frankenburg S, Londner MV, Greenblatt CL (1980) Cellular changes in the bone marrow ofPlasmodium berghei-infected mice. II. Blast transformation and phagocytosis. Cell Immunol 55:185–190
Kretschmar W, Jerusalem Ch (1963) Milz and malaria. Der Infektionsverlauf (Plasmodium berghei) in splenektomierten NMR-Mäusen und seine Deutung anhand der histopathologischen veränderungen der Milz nichtsplenektomierter Mäuse. Z Tropenmed Parasitol 14:279–310
Playfair JHL, De Souza JB, Dockrell HM, Agomo PU, Taverne J (1979) Cell-mediated immunity in the liver of mice vaccinated against malaria. Nature 282:731–734
Rencricca NJ, Coleman RM (1979) Altered erythropoiesis during the course of virulent murine malaria. Proc Soc Exp Biol Med 162:424–428
Schiffman E, Gallin JI (1979) Biochemistry of phagocyte chemotaxis. In: Horecker BL, Stadtman ER (eds) Current topics in cellular regulation. Academic Press 15:203–261
Snyderman R, Altman LC, Hausman MS, Mergenhagen SE (1972) Human mononuclear leukocyte chemotaxis: A quantitative assay for humoral and cellular chemotactic factors. J Immunol 108:857–861
Snyderman R, Phillips JK, Mergenhagen SE (1971) Biological activity of complement in vivo. Role of C5 in the accumulation of polymorphonuclear leukocytes in inflammatory exudates. J Exp Med 134:1131–1143
Srichaikul T, Panikbutr N, Jeumtrakul P (1965) Bone-marrow changes in human malaria. Ann Trop Med Parasitol 61:40–51
Ward PA (1971) Complement-derived leukotactic factors in pathological fluids. J Exp Med 134:109s-113s
Wasserman SI, Goetzl EJ, Ellman L, Austen KF (1974) Tumor-associated eosinophilotactic factor. N Engl J Med 290:420–424
Weissberger H, Golenser J, Spira DT (1979) Soluble antigens released in vitro from erythrocytes infected withPlasmodium berghei. Bull WHO 57:Suppl 1, 483
Wyler DJ, Gallin JI (1977) Spleen derived mononuclear cell chemotactic factor in malaria infections: A possible mechanism for splenic macrophage accumulation. J Immunol 118:478–484
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Frankenburg, S., Londner, M.V. & Greenblatt, C.L. Cellular changes in bone marrow of malaria-infected mice. Z. Parasitenkd. 68, 39–45 (1982). https://doi.org/10.1007/BF00926656
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DOI: https://doi.org/10.1007/BF00926656