Abstract
Plasma cell migration is crucial to immunity, but little is known about the molecular regulators of their migratory programs. Here, we detail the critical role of the transcription factor c-Myb in determining plasma cell location. In the absence of c-Myb, no IgG(+) antigen-specific plasma cells were detected in the bone marrow after immunization or virus infection. This was correlated with a dramatic reduction of plasma cells in peripheral blood, mislocalization in spleen, and an inability of c-Myb-deficient plasma cells to migrate along a CXCL12 gradient. Therefore, c-Myb plays an essential, novel role in establishing the long-lived plasma cell population in the BM via responsiveness to chemokine migration cues.
| Original language | English |
|---|---|
| Pages (from-to) | 1001 - 1009 |
| Number of pages | 9 |
| Journal | Journal of Experimental Medicine |
| Volume | 212 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 2015 |
| Externally published | Yes |
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