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Interleukin 4 increases CCR9 expression and homing of lymphocytes to gut-associated lymphoid tissue in chickens.
Annamalai, Thavamathi; Selvaraj, Ramesh K.
Affiliation
  • Annamalai T; Department of Animal Sciences, Ohio Agricultural Research and Development Center, Wooster, OH 44691, USA.
Vet Immunol Immunopathol ; 145(1-2): 257-63, 2012 Jan 15.
Article in En | MEDLINE | ID: mdl-22197009
ABSTRACT
The effects of in vitro and in vivo IL-4 supplementation on thymocyte and splenocyte CCR9 mRNA amount and migration were studied. Thymocytes, splenocytes, splenocytes+thymocytes (21), and splenocytes+bursocyte cells (21) were supplemented with either 0 or 5 ng/ml IL-4 for 5d. CCR9 mRNA was undetectable in all experimental groups supplemented with 0 ng/ml IL-4. IL-4 treatment (5 ng/ml) upregulated (P=0.01) CCR9 mRNA only in the splenocyte+thymocyte cell culture. IL-4-mediated CCR9 mRNA induction in the splenocyte+thymocyte cell culture was dependent on the in vitro dose of IL-4 supplementation. IL-4-treated splenocyte+thymocyte cells when injected in vivo preferentially migrated to cecal tonsils. In vivo supplementation of IL-4 was achieved through in ovo injection of recombinant chicken IL-4 plasmid. Cecal tonsils in chicks hatched from IL-4-plasmid-injected eggs weighed more, had a higher amount of CCR9 mRNA, and had a higher percentage of CD8(+) cells than cecal tonsils from chicks hatched from PBS-injected eggs. It could be concluded that IL-4 induces CCR9 mRNA in thymocytes and splenocytes and directs the migration of cells to gut-associated lymphoid tissue.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spleen / Thymus Gland / Lymphocytes / Interleukin-4 / Receptors, CCR Type of study: Risk_factors_studies Limits: Animals Language: En Journal: Vet Immunol Immunopathol Year: 2012 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spleen / Thymus Gland / Lymphocytes / Interleukin-4 / Receptors, CCR Type of study: Risk_factors_studies Limits: Animals Language: En Journal: Vet Immunol Immunopathol Year: 2012 Document type: Article Affiliation country: United States