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Each lymphocyte bears receptors that bind to a specific antigen.
Each lymphocyte produces its own specific receptor, which is structurally organized so that it responds to a different antigen.
MV infection levels within each lymphocyte subset were assessed by detection of cells expressing MV-N and shown as percentages.
As each lymphocyte matures, these gene segments are pieced together to form one gene for each polypeptide that makes up a specific antigen receptor.
Although they have only a small amount of cytoplasm compared with other cells, each lymphocyte has sufficient cytoplasmic organelles (small functional units such as mitochondria, the endoplasmic reticulum, and a Golgi apparatus) to keep the cell alive.
The essential components for generating an antibody response include B and T cell recognition of antigen, subsequent activation, clonal expansion of each lymphocyte type and migration of T cells into B cell follicles to provide help, all leading to germinal centre formation and antibody production.
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In each, lymphocytes congregate around the bile ducts.
However, when comparing a_cell types with one another, the "core UP" gene set was significantly induced to higher levels in each activated DC subset as compared with each activated lymphocyte subset (Supporting Information Fig. 4).
PBMCs were stimulated for 15 min, corresponding to the peak of response (data not shown), and then analysed simultaneously for each T lymphocyte subset.
The genetic rearrangement takes place at the stage when the lymphocytes generated from stem cells first become functional, so that each mature lymphocyte is able to make only one type of receptor.
Tremendous recent progress in our understanding of the interface between the T cell receptor (TCR) and peptide/MHC complexes has revealed a vast potential for degenerate recognition of numerous structurally similar pMHC complexes by each T lymphocyte.
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