The colony-stimulating factor 1 receptor is expressed on dendritic cells during differentiation and regulates their expansion


Autoria(s): MacDonald, Kelli P. A.; Rowe, Vanessa; Bofinger, Helen. M.; Thomas, Ranjeny; Sasmono, Tedjo; Hume, David A.; Hill, Geoffrey R.
Data(s)

01/08/2005

Resumo

The lineage of dendritic cells (DC), and in particular their relationship to monocytes and macrophages, remains obscure. Furthermore, the requirement for the macrophage growth factor CSF-1 during DC homeostasis is unclear. Using a transgenic mouse in which the promoter for the CSF-1R (c-fms) directs the expression of enhanced GFP in cells of the myeloid lineage, we determined that although the c-fms promoter is inactive in DC precursors, it is up-regulated in all DC subsets during differentiation. Furthermore, plasmacytoid DC and all CD11c(high) DC subsets are reduced by 50-70% in CSF-1-deficient osteopetrotic mice, confirming that CSF-1 signaling is required for the optimal differentiation of DC in vivo. These data provide additional evidence that the majority of tissue DC is of myeloid origin during steady state and supports a close relationship between DC and macrophage biology in vivo.

Identificador

http://espace.library.uq.edu.au/view/UQ:78213

Idioma(s)

eng

Publicador

American Association of Immunologists

Palavras-Chave #Immunology #M-csf Receptor #Op Op Mouse #Growth-factor #Gm-csf #Macrophages #Osteopetrosis #Progenipoietin-1 #Progenitors #Substitute #Support #C1 #320207 Autoimmunity #730102 Immune system and allergy #320202 Cellular Immunology
Tipo

Journal Article