T cell development Flashcards
What lineage of cells gives rise to T cells?
From where do they originate?
Pluripotent hematopoietic stem cells in the bone marrow.
Where do the precursors of T cells finish their maturation?
As a fetus before birth: in the fetal liver
As an adult later in life: in the THYMUS (just above the heart)
How do the HSCs commit to the T cell lineage?
- Interaction with thymic stromal cells → IL-7 production by thymic stromal cells → **IL-7 binding to the IL-7 receptor **on CD34+ progenitor cells
- Notch-1 on the surface of thymocytes interacts with ligands on thymic epithelial cells
- GATA3
Stages of T cell development
- HSC/CLP
- Progenitor-T cell (Pro-T; DN)
- Precursor-T cell (Pre-T; DN with Pre-TCRbeta and surrogate alpha)
- Double Positive (DP)
- Single Positive (SP) [aka Immature T cell]
- Mature T cell
The transition from Pro-T (DN) stage to the DP stage is mediated by…
- IL-2
- IL-7
- Notch
What happens between the Pro-T and Pre-T stages?
- First, proliferation of Pro-T cells
- Then, TCR gene rearrangement!!
- γδ rearrangements “race with” β rearrangement
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γδ - must undergo two rearrangements total
- for this reason, they usually don’t “win the race”
- Once they develop, γδ DNs are committed, leave the thymus immediately, and travel to the epithelial surfaces (e.g., gut/intestines)
-
β - only undergoes one reaarangement
- β-chain undergoes VDJ recombination
- Then, the β-chain translocates to the ER → β-chain’s ability to bind Pre-T-α is tested → “correct” β and Pre-T-α heterodimer is moved to the cell membrane → Pre-T-cell receptors
- Cell is now called a Pre-T cell and is is DN with a surrogate alpha
- During both of these rearrangements RAG and TdT are expressed
What happens between the Pre-Tα and DP stages?
- First, proliferation (no RAG or TdT expressed)!
- So that you have lots of Pre-T cells to try out the newly rearranged α-segment – this helps ⇡ diversity
- During proliferation, **CD4 **and CD8 begin being expressed, so that the cells are now DP thymocytes
- Then, α-chain rearrangement
- Cells move into the **inner cortex **of the thymus → reactivation of rearrangement machinery → RAG and TdT expression
- α-chain = light chain; only undergoes VJ recombination
- Each new α-chain is tested for its ability to bind the β chain → assembly of αβ TCRs
- Since δ gene is within the α gene, even if the Pre-Tα DN cells weren’t already commited to having αβ TCRs, they could not go back to become γδ TCRs since RAG will cut out the δ gene at this point
What happens between the DP and SP stage?
-
Positive selection!
- Occurs in the thymic cortex
- Thymic cortical epithelial cells present self-peptides on MHC I and II
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Can the cells bind the MHC molecules?
- If no, then the cells die!
- Additional α-chain rearrangement is permitted if there is no MHC interaction at first, but after 3-4 days w/o binding the cells apoptose
- Thymic MØs clear the debris
- If yes, they survive:
- If they bind MHCI → become CD8+ immature T cell
- If they bind MHCII → become CD4+ immature T cell
- This is called MHC restriction → SP T cells
- If no, then the cells die!
How does a SP immature T cell become a mature, but naive T cell?
-
Negative selection! (aka CENTRAL tolerance)
- Purpose of negative selection is to check for SP T cells that bind so tightly to self antigen that they could trigger an autoimmune response
- Occurs in the thymic medulla and several cell types present self-peptide MHC to the SP T cells, predominantly
- Bone marrow derived DCs and MØs
- Thymic DCs and mTECs express AutoImmune REgulator (AIRE), the transcription factor that mediates negative selection
- AIRE helps generate Tissue Reactive Antigens (TRAs) that will be “presented” on the surface of thymic DCs and mTECs
- A “self-reactive” T cell that binds to these TRAs on the thymic DCs and mTECs will undergo apoptosis
- Generates mature, but naive T cells
- Do I bind self antigen presented on the thymic DCs or mTECs?
- Yes → die!
- No → Keep → Travel to 2° lymphoid tissues and become activated effector T cells
Peripheral Tolerance
Peripheral tolerance develops after T and B cells mature and enter the periphery (secondary lymphoid organs). It involves:
- Suppression of autoreactive cells by Tregs
- Generation of lymphocyte anergy when they encounter antigen in the absence of the co-stimulatory signals