Abstract
CD5+ B lymphocytes have distinct functional properties compared with B lymphocytes that lack CD5. However, it remains unclear if and how the CD5 molecule modulates B lymphocyte biology and responses. Our recent studies have revealed that CD5 promotes constitutive activation of multiple signaling pathways including extracellular signal-regulated kinases (ERK1/2), phosphatidylinositol 3-kinase (PI-3K)/mammalian target of rapamycin (mTOR) and calcineurin-NFAT signaling pathways. Further, changes in cytokine production including the production of IL-10 are related to the activation of the transcription factors NFAT2 and STAT3. All in all, these studies provide a framework for understanding how CD5 impacts B lymphocyte biology and responses.
| Original language | English |
|---|---|
| Pages (from-to) | 795-798 |
| Number of pages | 4 |
| Journal | Autoimmunity Reviews |
| Volume | 11 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Sept 2012 |
| Externally published | Yes |
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