Characterization of Background Anti-Trinitrophenyl Plaque-Forming Cells Observed in Several Strains of Mice
Autor: | Takehiko Uchiyama, Ryozo Maeda, Noboru Yamaura |
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Rok vydání: | 1976 |
Předmět: |
medicine.medical_specialty
Ontogeny Hemolytic Plaque Technique Mice Inbred Strains chemical and pharmacologic phenomena Nitrophenols Mice Antigenic stimulation Immune system Internal medicine medicine Animals Avidity Antibody-Producing Cells Neonatal thymectomy Mice Inbred BALB C Mice Inbred C3H Mice Inbred ICR Chemistry Horse hemic and immune systems General Medicine Thymectomy eye diseases Mice Inbred C57BL Endocrinology nervous system Immunization Immunology tissues Spleen Icr mice |
Zdroj: | Japanese Journal of Microbiology. 20:45-52 |
ISSN: | 0021-5139 |
DOI: | 10.1111/j.1348-0421.1976.tb00906.x |
Popis: | Normal mice have a large number of background anti-trinitrophenyl (TNP) antibody-forming cells (AFC) in their spleens (about 40-50 anti-TNP PFC/10(6) cells). We investigated this among several mouse strains, i.e., C57BL/6, C3H/He, Balb/c, ddd, and ICR mice, and found that all strains had a similar number of anti-TNP PFC (plaque-forming cells). Developmental aspects of background anti-TNP PFC in the ontogenic process were also investigated. The number of anti-TNP PFC increased logari thmically during the first few days of age, reached a peak on the 13th day and attained a constant value within 30 days. Neonatal thymectomy did not decrease the number of background anti-TNP PFC but such treatment decreased the anti-TNP PFC response to TNP-HRBC (horse red blood cells) immunization. Germ-free ICR mice had a number of background anti -TNP PFC similar to that of conventional ICR mice. Avidity of background anti-TNP PFC was compared among mice of several ages and it was shown that there were no differences among them. These results suggest that the occurrence of these background anti-TNP PFC is not elicited by the immune response but by the natural maturation of precursors of ACF without antigenic stimulation. |
Databáze: | OpenAIRE |
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