Abstract
Bone marrow cultures were established from mice undergoing parasitic eosinophilia after infection with Trichinella spiralis. In the presence of eosinophil-differentiation factor (EDF/IL-5) eosinophil precursor cells differentiated and could be identified and counted after a 7-day in vitro culture period. The EDF-bone marrow assay system was used to determine differences in bone marrow eosinophil precursor capacity between a number of inbred strains of mice. Bone marrow cultures from high peripheral eosinophil-response phenotype strains of mice (NIH, SWR & SJL) contained significantly greater numbers of eosinophil precursor cells than the low response strain C57BL/10. All congenic strains of mice with the B10 background, i.e. C57BL/10, B10.S, B10.BR and B10.G were found to have low eosinophil precursor capacity. Bone marrow cultures obtained from F1 hybrids (NIH x C57/BL10, SJL x C57/BL10 and SWR x C57BL/10) demonstrated high precursor numbers, indicating that low responsiveness is inherited as a recessive characteristic. When spleen cells from T. spiralis-infected, high and low responder strains of mice were stimulated in vitro with concanavalin A (Con A) or with parasite antigen, it was found that low responder phenotype strains produced quantities of two eosinophilopoietic lymphokines EDF and IL3, which were similar to, if not greater than high responder strains. This suggests that bone marrow precursor capacity and not T cell lymphokine release is an important limiting factor in determining strain-dependent eosinophilia.
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Selected References
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- Adelman N., Cohen S., Yoshida T. Strain variations in murine MIF production. J Immunol. 1978 Jul;121(1):209–212. [PubMed] [Google Scholar]
- Alizadeh H., Wakelin D. Genetic factors controlling the intestinal mast cell response in mice infected with Trichinella spiralis. Clin Exp Immunol. 1982 Aug;49(2):331–337. [PMC free article] [PubMed] [Google Scholar]
- Basten A., Beeson P. B. Mechanism of eosinophilia. II. Role of the lymphocyte. J Exp Med. 1970 Jun 1;131(6):1288–1305. doi: 10.1084/jem.131.6.1288. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Begley C. G., Lopez A. F., Nicola N. A., Warren D. J., Vadas M. A., Sanderson C. J., Metcalf D. Purified colony-stimulating factors enhance the survival of human neutrophils and eosinophils in vitro: a rapid and sensitive microassay for colony-stimulating factors. Blood. 1986 Jul;68(1):162–166. [PubMed] [Google Scholar]
- Grencis R. K., Riedlinger J., Wakelin D. L3T4-positive T lymphoblasts are responsible for transfer of immunity to Trichinella spiralis in mice. Immunology. 1985 Oct;56(2):213–218. [PMC free article] [PubMed] [Google Scholar]
- Grencis R. K., Riedlinger J., Wakelin D. Lymphokine production by T cells generated during infection with Trichinella spiralis. Int Arch Allergy Appl Immunol. 1987;83(1):92–95. doi: 10.1159/000234337. [DOI] [PubMed] [Google Scholar]
- Guy-Grand D., Dy M., Luffau G., Vassalli P. Gut mucosal mast cells. Origin, traffic, and differentiation. J Exp Med. 1984 Jul 1;160(1):12–28. doi: 10.1084/jem.160.1.12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoffenbach A., Lagrange P. H., Bach M. A. Strain variation of lymphokine production and specific antibody secretion in mice infected with Mycobacterium lepraemurium. Cell Immunol. 1985 Mar;91(1):1–11. doi: 10.1016/0008-8749(85)90026-7. [DOI] [PubMed] [Google Scholar]
- Ihle J. N., Keller J., Greenberger J. S., Henderson L., Yetter R. A., Morse H. C., 3rd Phenotypic characteristics of cell lines requiring interleukin 3 for growth. J Immunol. 1982 Oct;129(4):1377–1383. [PubMed] [Google Scholar]
- Lammas D. A., Mitchell L. A., Wakelin D. Adoptive transfer of enhanced eosinophilia and resistance to infection in mice by an in vitro generated T-cell line specific for Mesocestoides corti larval antigen. Parasite Immunol. 1987 Sep;9(5):591–601. doi: 10.1111/j.1365-3024.1987.tb00532.x. [DOI] [PubMed] [Google Scholar]
- Lammas D. A., Mitchell L. A., Wakelin D. Genetic control of eosinophilia in parasitic infections: responses of mouse strains to treatment with cyclophosphamide and parasite antigen. Int J Parasitol. 1988 Dec;18(8):1077–1085. doi: 10.1016/0020-7519(88)90078-1. [DOI] [PubMed] [Google Scholar]
- Lee T. D., Grencis R. K., Wakelin D. Specific cross-immunity between Trichinella spiralis and Trichuris muris: immunization with heterologous infections and antigens and transfer of immunity with heterologous immune mesenteric lymph node cells. Parasitology. 1982 Apr;84(Pt 2):381–389. doi: 10.1017/s0031182000044929. [DOI] [PubMed] [Google Scholar]
- McGarry M. P., Speirs R. S., Jenkins V. K., Trentin J. J. Lymphoid cell dependence of eosinophil response to antigen. J Exp Med. 1971 Sep 1;134(3 Pt 1):801–814. doi: 10.1084/jem.134.3.801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reed N. D., Wakelin D., Lammas D. A., Grencis R. K. Genetic control of mast cell development in bone marrow cultures. Strain-dependent variation in cultures from inbred mice. Clin Exp Immunol. 1988 Sep;73(3):510–515. [PMC free article] [PubMed] [Google Scholar]
- Sanderson C. J., Warren D. J., Strath M. Identification of a lymphokine that stimulates eosinophil differentiation in vitro. Its relationship to interleukin 3, and functional properties of eosinophils produced in cultures. J Exp Med. 1985 Jul 1;162(1):60–74. doi: 10.1084/jem.162.1.60. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sewell W. A., Vadas M. A. Evidence for the control of eosinophilia by the major histocompatibility complex in mice. Immunogenetics. 1983;17(2):167–177. doi: 10.1007/BF00364756. [DOI] [PubMed] [Google Scholar]
- Strath M., Sanderson C. J. Detection of eosinophil differentiation factor and its relationship to eosinophilia in Mesocestoides corti-infected mice. Exp Hematol. 1986 Jan;14(1):16–20. [PubMed] [Google Scholar]
- Strath M., Warren D. J., Sanderson C. J. Detection of eosinophils using an eosinophil peroxidase assay. Its use as an assay for eosinophil differentiation factors. J Immunol Methods. 1985 Nov 7;83(2):209–215. doi: 10.1016/0022-1759(85)90242-x. [DOI] [PubMed] [Google Scholar]
- Vadas M. A. Cyclophosphamide pretreatment induces eosinophilia to nonparasite antigens. J Immunol. 1981 Nov;127(5):2083–2086. [PubMed] [Google Scholar]
- Vadas M. A. Genetic control of eosinophilia in mice: gene(s) expressed in bone marrow-derived cells control high responsiveness. J Immunol. 1982 Feb;128(2):691–695. [PubMed] [Google Scholar]
- Vadas M. A. Newer aspects of regulation of human granulocyte function. Aust N Z J Med. 1984 Feb;14(1):71–74. doi: 10.1111/j.1445-5994.1984.tb03595.x. [DOI] [PubMed] [Google Scholar]
- Wakelin D., Donachie A. M. Genetic control of eosinophilia. Mouse strain variation in response to antigens of parasite origin. Clin Exp Immunol. 1983 Feb;51(2):239–246. [PMC free article] [PubMed] [Google Scholar]
- Wakelin D., Donachie A. M. Genetic control of immunity to Trichinella spiralis. Donor bone marrow cells determine responses to infection in mouse radiation chimaeras. Immunology. 1981 Aug;43(4):787–792. [PMC free article] [PubMed] [Google Scholar]
- Wakelin D., Donachie A. M. Genetic control of immunity to parasites: adoptive transfer of immunity between inbred strains of mice characterized by rapid and slow immune expulsion of Trichinella spiralis. Parasite Immunol. 1980 Winter;2(4):249–260. doi: 10.1111/j.1365-3024.1980.tb00057.x. [DOI] [PubMed] [Google Scholar]
- Wakelin D. Genetic control of immunity to helminth infections. Parasitol Today. 1985 Jul;1(1):17–23. doi: 10.1016/0169-4758(85)90101-2. [DOI] [PubMed] [Google Scholar]
- Wakelin D., Lloyd M. Immunity to primary and challenge infections of Trichinella spiralis in mice: a re-examination of conventional parameters. Parasitology. 1976 Apr;72(2):173–182. doi: 10.1017/s0031182000048472. [DOI] [PubMed] [Google Scholar]
- Wakelin D., Wilson M. M. Transfer of immunity to Trichinella spiralis in the mouse with mesenteric lymph node cells: time of appearance of effective cells in donors and expression of immunity in recipients. Parasitology. 1977 Jun;74(3):215–224. doi: 10.1017/s0031182000047843. [DOI] [PubMed] [Google Scholar]
- Warren D. J., Sanderson C. J. Production of a T-cell hybrid producing a lymphokine stimulating eosinophil differentiation. Immunology. 1985 Apr;54(4):615–623. [PMC free article] [PubMed] [Google Scholar]