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Thrombocyte migration and the release of thrombocyte inhibitory factor (ThrIF) by T and B cells in the chicken
The elaboration of various inhibitory factors by sensitized lymphocytes has been reported for both mammals and birds. Until recently, the ability of the B cell to elaborate these had been questioned by a number of investigators. We have demonstrated the release of a lymphocyte inhibitory factor from the avian thymus and bursal lymphocyte. The avian thrombocyte is active in haemostasis as well as being a phagocytic cell. We have demonstrated that the ability of the thrombocyte to migrate, significantly exceeded that of thymic lymphocytes. Sensitized T and B cells, as well as activated supernatants from these cells, were capable of inhibiting thrombocyte migration. Treatment of sensitized B cells with anti-T-cell serum plus complement failed to eliminate this cell's ability to block thrombocyte migration. These data attribute the capability of elaborating a thrombocyte migration inhibitory factor to both the avian thymic and bursal lymphocyte, and attribute a degree of maturity to these cells not previously demonstrated.
The elaboration of various inhibitory factors by sensitized lymphocytes has been reported for both mammals and birds. Until recently, the ability of the B cell to elaborate these had been questioned by a number of investigators. We have demonstrated the release of a lymphocyte inhibitory factor from the avian thymus and bursal lymphocyte. The avian thrombocyte is active in haemostasis as well as being a phagocytic cell. We have demonstrated that the ability of the thrombocyte to migrate, significantly exceeded that of thymic lymphocytes. Sensitized T and B cells, as well as activated supernatants from these cells, were capable of inhibiting thrombocyte migration. Treatment of sensitized B cells with anti-T-cell serum plus complement failed to eliminate this cell's ability to block thrombocyte migration. These data attribute the capability of elaborating a thrombocyte migration inhibitory factor to both the avian thymic and bursal lymphocyte, and attribute a degree of maturity to these cells not previously demonstrated.