CLEC5A (MDL-1) is a novel PU. 1 transcriptional target during myeloid differentiation

J Batliner, MM Mancarelli, M Jenal, VA Reddy… - Molecular …, 2011 - Elsevier
J Batliner, MM Mancarelli, M Jenal, VA Reddy, MF Fey, BE Torbett, MP Tschan
Molecular immunology, 2011Elsevier
C-type lectin domain family 5, member A (CLEC5A), also known as myeloid DNAX activation
protein 12 (DAP12)-associating lectin-1 (MDL-1), is a cell surface receptor strongly
associated with the activation and differentiation of myeloid cells. CLEC5A associates with
its adaptor protein DAP12 to activate a signaling cascade resulting in activation of
downstream kinases in inflammatory responses. Currently, little is known about the
transcriptional regulation of CLEC5A. We identified CLEC5A as one of the most highly …
C-type lectin domain family 5, member A (CLEC5A), also known as myeloid DNAX activation protein 12 (DAP12)-associating lectin-1 (MDL-1), is a cell surface receptor strongly associated with the activation and differentiation of myeloid cells. CLEC5A associates with its adaptor protein DAP12 to activate a signaling cascade resulting in activation of downstream kinases in inflammatory responses. Currently, little is known about the transcriptional regulation of CLEC5A. We identified CLEC5A as one of the most highly induced genes in a microarray gene profiling experiment of PU.1 restored myeloid PU.1-null cells. We further report that CLEC5A expression is significantly reduced in several myeloid differentiation models upon PU.1 inhibition during monocyte/macrophage or granulocyte differentiation. In addition, CLEC5A mRNA expression was significantly lower in primary acute myeloid leukemia (AML) patient samples than in macrophages and granulocytes from healthy donors. Moreover, we found activation of a CLEC5A promoter reporter by PU.1 as well as in vivo binding of PU.1 to the CLEC5A promoter. Our findings indicate that CLEC5A expression in monocyte/macrophage and granulocytes is regulated by PU.1.
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