| First Author | Meixner A | Year | 2008 |
| Journal | Nat Cell Biol | Volume | 10 |
| Issue | 8 | Pages | 1003-11 |
| PubMed ID | 18641637 | Mgi Jnum | J:145478 |
| Mgi Id | MGI:3834799 | Doi | 10.1038/ncb1761 |
| Citation | Meixner A, et al. (2008) Epidermal JunB represses G-CSF transcription and affects haematopoiesis and bone formation. Nat Cell Biol 10(8):1003-11 |
| abstractText | Mice that lack JunB in epidermal cells are born with normal skin; however, keratinocytes hyperproliferate in vitro and on TPA treatment in vivo. Loss of JunB expression in the epidermis of adult mice affects the skin, the proliferation of haematopoietic cells and bone formation. G-CSF is a direct transcriptional target of JunB and mutant epidermis releases large amounts of G-CSF that reach high systemic levels and cause skin ulcerations, myeloproliferative disease and low bone mass. The absence of G-CSF significantly improves hyperkeratosis and prevents the development of myeloproliferative disease, but does not affect bone loss. This study describes a mechanism by which the absence of JunB in epithelial cells causes multi-organ disease, suggesting that the epidermis can act as an endocrine-like organ. |
