Biology · MU Sofia

30. Central (primary) lymphoid organs. Lymphocyte differentiation in the central lymphoid organs. Acquisition of immune competence, selection of immature lymphocytes.

Covers how lymphocytes arise from haematopoietic stem cells in the bone marrow and then develop in the central lymphoid organs. It walks through B cell development in marrow niches, including immunoglobulin heavy and light chain rearrangement, receptor editing and negative selection, then T cell development in the thymus from double negative to single positive stages, with positive and negative selection. It ends with thymic involution and CD4 T cell subsets such as Tregs and Th17, and includes four mnemonics summarising the stages.

Inside: 8 sections · 2 labelled pictures · 8 min

Topic 30 of 64 in the MU Sofia syllabus for Biology (Dental Medicine, Year 1). The free AceMed note covers it in 8 sections, about 1,204 words (8 min of reading).

In this note

  1. Lymphocyte differentiation in central lymphoid organs.
  2. Origin of Lymphocytes
  3. Central or Primary Lymphoid Organs
  4. B Cell Differentiation in the Bone Marrow
  5. T Cell Differentiation in the Thymus
  6. Thymus Involution
  7. Subsets of CD4 Positive T Cells
  8. MNEMONIC

Origin of Lymphocytes

  • All lymphocytes begin their development from pluripotent hematopoietic stem cells located in the bone marrow
  • These stem cells give rise to multipotent progenitor cells which further differentiate into:
  • Common myeloid progenitors that lead to the myeloid lineage
  • Multi-lymphoid progenitors that give rise to lymphoid cells
  • Some lymphoid progenitors remain in the bone marrow to become B cells or natural killer cells
  • Others leave the bone marrow and migrate to the thymus where they begin their journey to become T cells

Central or Primary Lymphoid Organs

  • The bone marrow and thymus are known as the central lymphoid organs
  • These organs are responsible for the generation and maturation of lymphocytes but do not participate in immune responses
  • The key function of these organs is to help immature lymphocytes develop antigen receptors, making them immunocompetent
  • This differentiation is known as antigen-independent because it occurs before the lymphocytes encounter any external antigen

B Cell Differentiation in the Bone Marrow

Structure and Environment

  • Bone marrow is located in the spongy cavities of bones and provides a nurturing environment for hematopoiesis
  • Differentiation of B cells occurs in specialized regions called niches which provide necessary growth signals
  • These niches are formed by interactions between developing cells and supportive stromal cells that create a three-dimensional network
  • Stromal cells regulate access to nutrients, oxygen, and survival signals and are essential for proper B cell development

Stages of B Cell Development

  • Common lymphoid progenitors commit to the B cell lineage and first become pro-B cells
  • Pro-B cells undergo rearrangement of the immunoglobulin heavy chain genes through VDJ recombination
  • This process is tightly regulated through allelic exclusion to ensure only one heavy chain is produced
  • If the first attempt fails, rearrangement is attempted on the second chromosome
  • If both attempts fail, the cell undergoes programmed cell death
  • Successfully rearranged pro-B cells become pre-B cells and begin rearranging the light chain genes (kappa first, followed by lambda if needed)
  • Once a functional light chain is produced, the B cell expresses surface IgM and becomes an immature B cell

Antigen Receptor Construction

  • The B cell receptor or BCR is not pre-encoded but is assembled from multiple gene fragments using VDJ recombination
  • Terminal deoxynucleotidyl transferase introduces random nucleotides at the junctions, contributing to antibody diversity
  • Successful assembly of the BCR is the hallmark of immunocompetence in B cells

Central Tolerance and Negative Selection

  • Immature B cells undergo a tolerance check to ensure they do not strongly react to self-antigens

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