Production of Macrophage Migration Inhibition Factors by Virus-Infected Cell Cultures

Author:

Flanagan Thomas D.1,Yoshida Takeshi1,Cohen Stanley1

Affiliation:

1. Departments of Microbiology and Pathology, and the Center for Immunology, State University of New York, Buffalo, New York 14214

Abstract

Macrophage migration inhibitory (MIF-like) activity was demonstrated in the supernatant fluids from cultures of African green monkey kidney cells (BGM) infected with mumps virus or Newcastle disease virus. We could detect no such activity in noninfected cultures. The virus-induced activity reported here is not due to nonspecific cytotoxic material released by dead or dying cells, and it does not require cell replication for its production. Preliminary estimates of molecular weight by Sephadex G-100 chromatography revealed a broad band of activity associated with the 45,000 and 65,000 markers. These are significantly smaller than previously reported chemotactic substances from virus-infected cultures, and thus appear to represent different cell products. These MIF-like factors may be produced concomitantly with interferon. However, ultraviolet irradiation of appropriate duration abolishes the ability of viruses to induce substances with MIF-like activity while preserving the ability to induce interferon. This strongly suggests that interferon is not the agent responsible for the macrophage migration inhibition effect. The functional properties of these various cell products induced by virus infection suggest that they all may play a role in the response to virus infection in vivo.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference21 articles.

1. Semi-micro, dye-binding assay for rabbit interferon;Armstrong J. A.;Appl. Microbiol.,1971

2. Characteristics of the BGM line of cells from African green monkey kidney;Barron A. L.;Arch. Gesamte Virusforsch.,1970

3. Dissociation of MIF production and cell proliferation;Bloom B. R.;J. Immunol.,1972

4. Migration inhibitory factor and the cellular basis of delayed-type hypersensitivity reactions;Bloom B. R.;Amer. J. Pathol.,1970

5. In vitro studies of cellular hypersensitivity. I. Specific inhibition of migration of cells from adjuvant-immunized animals by purified protein derivative and other protein antigens;Carpenter R. R.;J. Immunol.,1963

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