Thymocytes were incubated with antibody to CD8 (YTS169) and goat anti-rat Ig for 6 h and were fixed in ethanol overnight

Thymocytes were incubated with antibody to CD8 (YTS169) and goat anti-rat Ig for 6 h and were fixed in ethanol overnight. capable of a low-affinity connection with sponsor MHC molecules, and self peptides fail positive selection and are eliminated. The mechanism by which cells that do not pass positive selection are eliminated is usually termed death by neglect, Death by neglect has not been defined, but as the name indicates, it is generally considered to result from a lack of cytokines or additional growth factors delivered to the cell. The cytokines IL-2 and IL-7 up-regulate antiapoptotic proteins and enhance the survival of thymocytes (5C7). Death receptors most likely do not play a role in death by neglect because the expression of a dominantnegative FADD molecule in thymocytes has no effect on apoptosis caused by cytokine withdrawal (8). Steroids have also been implicated in thymocyte survival. Whereas adrenalectomized mice have improved thymic cellularity (9), mice reconstituted with bone marrow deficient in the manifestation of the Rabbit polyclonal to AMACR glucocorticoid receptor have normal thymic cellularity and no apparent defects in death by overlook (10). The stalk region of CD8 ( and ) consists of a number of O-linked sugars (11) that undergo changes during the maturation of thymocytes. In particular, the O-linked carbohydrates on CD8 indicated by immature double-positive (DP) thymocytes are not sialylated (12). Accompanying the differentiation of DP thymocytes to CD8 single-positive (SP) cells, the sugars moieties on CD8 are extensively sialylated from the ARS-1323 enzyme ST3Gal-I sialytransferase and become negatively charged (13). The nonsialylated form of CD8 on immature DP ARS-1323 thymocytes has a higher affinity for MHC class I molecules and may bind MHC class I molecules in the absence of TCRCMHC class I relationships (14, 15). In contrast, there is no evidence the affinity of CD4 for MHC class II molecule changes during thymocyte development. Whether the changes in affinity of CD8 for MHC class I molecules during thymocyte development has a physiological part is definitely unclear. Jameson and coworkers (15) suggested that an increase in the affinity of CD8 for MHC class I molecules may enhance positive selection by increasing the connection between developing thymocytes and target cells. We have found that ligation of CD8 on a subpopulation of immature DP thymocytes, either with antibodies to CD8 or with MHC class I molecules, prospects to quick apoptosis. We have also found that treatment with antibodies to CD3 protects thymocytes from CD8-mediated apoptosis. We hypothesize the binding of CD8 to MHC class I molecules on immature thymocytes, in the absence of TCR engagement, prospects to the induction of apoptosis. This apoptotic stimulus may be a mechanism by which thymocytes that do not survive positive selection are eliminated. Materials and Methods Mice. C57BL/6 and B6.MHCC/C (AbC and 2MC two times knockout) mice were purchased from ARS-1323 Taconic Farms. Young (4- to 6-weeks older) mice were killed by CO2 asphyxiation. The thymus was eliminated and a single-cell suspension was prepared by passage through a 0.2-m cell strainer (Fisher) and resuspended in MEM plus 10% FCS. Crosslinking of CD8 with Antibodies. Thymocytes at 1 107 cells per ml were incubated with antibodies to either CD8 (clone 53C6.7.2 or YTS169), CD4 (clone GK1.5), or CD8 (clone 53C5.8) at a final concentration of 10 g/ml inside a volume of 100 l in individual wells of a flat bottom 96-well tradition plate (Fisher). To crosslink the antibodies, 50 g/ml goat anti-rat Ig (Jackson Immunolabs, Western Grove, PA) was added to the cultures. Like a positive control for apoptosis, cells were incubated with 1 M dexamethasone (Sigma). Cells were incubated at 37C for 3C6 h, washed with PBS, and stained with annexin V-FITC (Biosource International, Camarillo, CA) and 0.5 g/ml propidium iodide (PI; Sigma) and analyzed by circulation cytometry. Crosslinking of CD8 ARS-1323 with Biotinylated Antibodies on Sorted Populations. C57BL/6 thymocytes were stained with antibodies to CD8.