CSF1R Is Required for Differentiation and Migration of Langerhans Cells and Langerhans Cell Histiocytosis

• Published in: Cancer immunology research Vol. 8; no. 6; p. 829
• Main Authors: Lonardi, Silvia, Scutera, Sara, Licini, Sara, Lorenzi, Luisa, Cesinaro, Anna Maria, Gatta, Luisa Benerini, Castagnoli, Carlotta, Bollero, Daniele, Sparti, Rosaria, Tomaselli, Michela, Medicina, Daniela, Calzetti, Federica, Cassatella, Marco Antonio, Facchetti, Fabio, Musso, Tiziana, Vermi, William
• Format: Journal Article
• Language: English
• Published: United States 01.06.2020
• Subjects: Adolescent; Adult; Aged; Apoptosis; Cell Differentiation; Cell Lineage; Cell Movement; Cells, Cultured; Child; Child, Preschool; Dendritic Cells - metabolism; Dendritic Cells - pathology; Female; Histiocytosis, Langerhans-Cell - metabolism; Histiocytosis, Langerhans-Cell - pathology; Humans; Infant; Infant, Newborn; Langerhans Cells - metabolism; Langerhans Cells - pathology; Male; Middle Aged; Monocytes - metabolism; Monocytes - pathology; Receptor, Macrophage Colony-Stimulating Factor - metabolism; Tumor Microenvironment; Young Adult
• ISSN: 2326-6074
• DOI: 10.1158/2326-6066.cir-19-0232

Langerhans cell histiocytosis (LCH) is a rare disorder characterized by tissue accumulation of CD1a CD207 LCH cells. In LCH, somatic mutations of the gene have been detected in tissue LCH cells, bone marrow CD34 hematopoietic stem cells, circulating CD14 monocytes, and BDCA1 myeloid dendritic cells (DC). Targeting in clonal Langerhans cells (LC) and their precursors is a potential treatment option for patients whose tumors have the mutation. The development of mouse macrophages and LCs is regulated by the CSF1 receptor (CSF1R). In patients with diffuse-type tenosynovial giant cell tumors, CSF1R inhibition depletes tumor-associated macrophages (TAM) with therapeutic efficacy; however, CSF1R signaling in LCs and LCH has not been investigated. We found through IHC and flow cytometry that CSF1R is normally expressed on human CD1a CD207 LCs in the epidermis and stratified epithelia. LCs that were differentiated from CD14 monocytes, BDCA1 DCs, and CD34 cord blood progenitors expressed CSF1R that was downregulated upon maturation. Immature LCs migrated toward CSF1, but not IL34. Administration of the c-FMS/CSF1R kinase inhibitors GW2580 and BLZ945 significantly reduced human LC migration. In LCH clinical samples, LCH cells (including cells) and TAMs retained high expression of CSF1R. We also detected the presence of transcripts for its ligand, CSF1, but not IL34, in all tested LCH cases. CSF1R and CSF1 expression in LCH, and their role in LC migration and differentiation, suggests CSF1R signaling blockade as a candidate rational approach for treatment of LCH, including the and wild-type forms of the disease.