Activation and Cell Cycle Control of Murine B Lymphocytes (original) (raw)
1985, Journal of Cell Science
The cell cycle of activated murine B lymphocytes (B cells) is controlled by the occupancy of surface membrane-bound immunoglobulin (Ig) and by two types of growth factors, called a and /3factors. These growth factors are produced in an endocrine fashion by the interaction of helper T lymphocytes (T cells) with antigen-presenting macrophages (A cells). Antigen is taken up, pro cessed and presented on the surface of A cells in the context of class II major histocompatibility complex (MHC) glycoproteins. Helper Tcells recognize this association of antigen and class II MHC molecules. A cells produce »factors and T cells produce /S factors. The molecular nature of these factors and of the corresponding receptors on B cells has yet to be elucidated, although it can be shown that the complement component C3d replaces a factor action. Resting, Go phase B cells are refractory to the action of or and /3 factors. They have to be excited, i.e. rendered susceptible to the action of these factors. This can be achieved by the interaction with helper T cells that recognize antigen, bound by surface membrane Ig, in the context of class II MHC glycoproteins on the surface of resting Go B cells. Excitation can also occur in a polyclonal fashion by cross-linking of suface Ig with immobilized, Ig-specific antibodies, or by the interaction with polyclonal activators of B cells, such as lipopolysaccharides. Entry into the cell cycle is asynchronous. Activated, cycling B cells can be synchronized by size separation, using velocity sedimentation. Synchronized B cells will retain their synchrony for several divisions, when they are stimulated by immobilized Ig-specific antibodies, o'and)3factors. They divide every 20 h at 37 °C. Omission of either of the three stimuli arrests B cells, though at different points in the cell cycle. Three restriction points are found: the first occurs immediately after mitosis and is controlled by the binding of immobilized Ig-specific antibodies to surface membrane-bound Ig. The second is observed in the Gy phase, around 6-8 h after mitosis and 2-4 h before entry into 5 phase. It is controlled by a factors. The third is found 2-4 h before mitosis, in Gz phase, and is controlled by Pfactors.