IL-12 promotes the accessory cell function of epidermal Langerhans cells. 1998

Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
Fujisaki Institute, Hayashibara Biochemical Laboratories, Inc., Okayama, Japan.

The objective of this study was to investigate the effects of cytokines regulating cutaneous immune responses, on the accessory cell function of epidermal cells (EC). EC were treated with various cytokines, and the accessory cell function of the cytokine-pretreated EC was examined by the allogeneic mixed epidermal cell-lymphocyte reaction (MECLR). Among the cytokines examined, IFN-gamma- and IL-12-pretreated EC augmented IFN-gamma production in the MECLR, while none of the other cytokines was effective. However, the cytokine-pretreated EC did neither affect T cell proliferation nor IL-4 production in the MECLR. Next we attempted to analyze the mechanisms by which IL-12-pretreated EC increase IFN-gamma production in the MECLR. Endogenous IFN-gamma produced during the IL-12 pretreatment of EC was found to play only a minor role in modulating the function of EC. The expression of MHC class II, CD80 and CD86 on EC was not affected by IL-12. On the other hand, soluble mediators that induce IFN-gamma production during the MECLR containing IL-12-pretreated EC were identified as endogenously produced IL-12 (the major mediator) and IL-18 (the minor mediator). Furthermore, the results of depletion experiments indicate that IL-12 promotes the accessory cell function of Langerhans cells to responder T cells in inducing IFN-gamma production in the MECLR.

UI MeSH Term Description Entries
D007371 Interferon-gamma The major interferon produced by mitogenically or antigenically stimulated LYMPHOCYTES. It is structurally different from TYPE I INTERFERON and its major activity is immunoregulation. It has been implicated in the expression of CLASS II HISTOCOMPATIBILITY ANTIGENS in cells that do not normally produce them, leading to AUTOIMMUNE DISEASES. Interferon Type II,Interferon, Immune,gamma-Interferon,Interferon, gamma,Type II Interferon,Immune Interferon,Interferon, Type II
D007801 Langerhans Cells Recirculating, dendritic, antigen-presenting cells containing characteristic racket-shaped granules (Birbeck granules). They are found principally in the stratum spinosum of the EPIDERMIS and are rich in Class II MAJOR HISTOCOMPATIBILITY COMPLEX molecules. Langerhans cells were the first dendritic cell to be described and have been a model of study for other dendritic cells (DCs), especially other migrating DCs such as dermal DCs and INTERSTITIAL DENDRITIC CELLS. Langerhans Cell,Dendritic Cells, Dermal,Dendritic Cells, Epidermal,Dendritic Cells, Skin,Dermal Dendritic Cells,Epidermal Dendritic Cells,Skin Dendritic Cells,Cell, Dermal Dendritic,Cell, Epidermal Dendritic,Cell, Langerhans,Cell, Skin Dendritic,Cells, Dermal Dendritic,Cells, Epidermal Dendritic,Cells, Langerhans,Cells, Skin Dendritic,Dendritic Cell, Dermal,Dendritic Cell, Epidermal,Dendritic Cell, Skin,Dermal Dendritic Cell,Epidermal Dendritic Cell,Skin Dendritic Cell
D008807 Mice, Inbred BALB C An inbred strain of mouse that is widely used in IMMUNOLOGY studies and cancer research. BALB C Mice, Inbred,BALB C Mouse, Inbred,Inbred BALB C Mice,Inbred BALB C Mouse,Mice, BALB C,Mouse, BALB C,Mouse, Inbred BALB C,BALB C Mice,BALB C Mouse
D008809 Mice, Inbred C3H An inbred strain of mouse that is used as a general purpose strain in a wide variety of RESEARCH areas including CANCER; INFECTIOUS DISEASES; sensorineural, and cardiovascular biology research. Mice, C3H,Mouse, C3H,Mouse, Inbred C3H,C3H Mice,C3H Mice, Inbred,C3H Mouse,C3H Mouse, Inbred,Inbred C3H Mice,Inbred C3H Mouse
D004817 Epidermis The external, nonvascular layer of the skin. It is made up, from within outward, of five layers of EPITHELIUM: (1) basal layer (stratum basale epidermidis); (2) spinous layer (stratum spinosum epidermidis); (3) granular layer (stratum granulosum epidermidis); (4) clear layer (stratum lucidum epidermidis); and (5) horny layer (stratum corneum epidermidis).
D005260 Female Females
D000078404 Epidermal Cells Cells from the outermost, non-vascular layer (EPIDERMIS) of the skin. Epidermal Cell,Epidermic Cells,Cell, Epidermal,Cell, Epidermic,Cells, Epidermic,Epidermic Cell
D000276 Adjuvants, Immunologic Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. Immunoactivators,Immunoadjuvant,Immunoadjuvants,Immunologic Adjuvant,Immunopotentiator,Immunopotentiators,Immunostimulant,Immunostimulants,Adjuvant, Immunologic,Adjuvants, Immunological,Immunologic Adjuvants,Immunological Adjuvant,Adjuvant, Immunological,Immunological Adjuvants
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013601 T-Lymphocytes Lymphocytes responsible for cell-mediated immunity. Two types have been identified - cytotoxic (T-LYMPHOCYTES, CYTOTOXIC) and helper T-lymphocytes (T-LYMPHOCYTES, HELPER-INDUCER). They are formed when lymphocytes circulate through the THYMUS GLAND and differentiate to thymocytes. When exposed to an antigen, they divide rapidly and produce large numbers of new T cells sensitized to that antigen. T Cell,T Lymphocyte,T-Cells,Thymus-Dependent Lymphocytes,Cell, T,Cells, T,Lymphocyte, T,Lymphocyte, Thymus-Dependent,Lymphocytes, T,Lymphocytes, Thymus-Dependent,T Cells,T Lymphocytes,T-Cell,T-Lymphocyte,Thymus Dependent Lymphocytes,Thymus-Dependent Lymphocyte

Related Publications

Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
November 1986, Scandinavian journal of immunology,
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
April 1988, Transplantation proceedings,
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
June 1988, Journal of immunology (Baltimore, Md. : 1950),
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
March 1984, Journal of immunology (Baltimore, Md. : 1950),
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
February 1996, Journal of immunology (Baltimore, Md. : 1950),
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
April 1986, British journal of experimental pathology,
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
November 1992, The Journal of investigative dermatology,
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
January 1980, Immunological reviews,
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
May 2013, The Journal of investigative dermatology,
Y Suemoto, and O Ando, and M Kurimoto, and T Horikawa, and M Ichihashi
September 2004, Journal of leukocyte biology,
Copied contents to your clipboard!