The relationship between endocytosis of concanavalin A and phytohaemagglutinin receptors and blast transformation, and direct identification of individual rabbit lymphocytes reactive to both mitogens.
نویسندگان
چکیده
Distribution and modulation of rabbit lymphocyte phytohaemagglutinin acceptors and concanavalin A acceptors during activation of rabbit lymphocytes have been examined by electron microscopy. Two types of cell surface acceptors have been tentatively identified, lectin binding acceptors that do not modulate, and receptors that are endocytosed when blast transformation is stimulated. All of the cells have binding acceptors for both lectins. Endocytosis correlates with early blast transformation and serves as an early marker for lymphocyte activation. When examined after 24 h of culture, those cells that undergo blast transformation contain endocytosed lectin receptors, whereas small untransformed cells do not. Capping prior to endocytosis is rarely observed. The mechanism whereby the signal for transformation is maintained after the reaction of lectin with cell surface receptors and transposed to the nucleus is not known. Although we conclude that endocytosis is an early event required for cell activation, it is possible that endocytosis is secondary to other activation events. By evaluation of sequential endocytosis, individual rabbit lymphocytes that endocytose only concanavalin A, only phytohaemagglutinin, both concanavalin A and phytohaemagglutinin, or neither lectin, have been identified.
منابع مشابه
Effects of insulin on phytohemagglutinin-P, concanavalin-A, and pokeweed mitogen in diabetic and nondiabetic lymphocytes.
Blast transformation of lymphocytes from diabetics and nondiabetics was evaluated after adding insulin at various concentrations. Responses to phytohemagglutinin-P (PHA-P), concanavalin-A (CON-A) and pokeweed mitogen (PWM) were measured in the presence of exogenous insulin added in physiologic increments of 0, 10, 20, 30, and 40 microunits of activity per ml of culture medium. A modified method...
متن کاملImmunoglobulin Molecules on the Surface of Activated T Lymphocytes in the Rat
Lewis strain rat lymphocytes were exposed in vitro to a variety of specific and nonspecific blastogenic stimuli. The surfaces of the transformed lymphocytes were examined by indirect immunofluorescence for the presence of T cell antigens and immunoglobulin molecules. More than 90% of lymphocytes that underwent blast transformation after exposure to foreign histocompatibility antigens (mixed lym...
متن کاملRelationship between enhanced turnover of phosphatidylinositol and lymphocyte activation by mitogens.
1. Various lectins [phaseolus vulgaris phytohaemagglutinin, Glycine max (soy-bean) agglutinin, Triticum vulgaris (wheat-germ) agglutinin and Axinella polyploides agglutinin] and antibodies to pig Ig (immunoglobulin) that are found by pig lymphocytes were assessed in terms of their capacities to stimulate lymphocyte transformation and to enhance phosphatidylinositol turnover. Transformation was ...
متن کاملSpecific Adherence of in Vitro Differentiated Lymphocytes to Target Cells
Blast cells which were derived from rat lymphocytes by stimulation with phytohemagglutinin (PHA), concanavalin A (Con A), or pokeweed mitogen (PWM) transformed within 2-3 days into a new type of lymphocytes when plated without mitogen on embryo fibroblast monolayers. These lymphocytes were termed secondary lyrophocytes. Upon addition of PWM to PWM-secondary lymphocytes a marked adherence to fib...
متن کاملChanges in some pro-and anti-inflammatory cytokines produced by bovine peripheral blood mononuclear cells following foot and mouth disease vaccination
Interleukin (IL)-17 is exclusively produced by CD4 helper T-cells upon activation. It most often acts as a pro-inflammatory cytokine, which stimulates the release of pro-inflammatory cytokines IL-6, IL-8, TNF-α, and granulocyte-macrophage colony-stimulating factor (GM-CSF). In this study, we studied the in-vitro IL-17 response to specific antigens and a variety of mitogens and compared the IL-1...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Journal of cell science
دوره 56 شماره
صفحات -
تاریخ انتشار 1982