TY - JOUR
T1 - Human plasmacytoid dendritic cells express an atrial natriuretic peptide receptor, guanylyl cyclase-A
AU - Morita, Rimpei
AU - Fujita, Tomoko
AU - Uchiyama, Takashi
AU - Hori, Toshiyuki
PY - 2009/7
Y1 - 2009/7
N2 - Atrial natriuretic peptide is a cardiovascular hormone secreted mainly by the cardiac atria and regulates the volume-pressure homeostasis. The action of ANP is mediated by GC-A.We previously reported that human monocyte-derived dendritic cells express GC-A and respond to ANP with polarization toward a Th2-inducing phenotype. In the present study, we explored the possibility that pDC are subjected to immunoregulation via the ANP/GC-A system.We examined GC-A expression on blood pDC and found that GC-A was not expressed on fresh pDC but was induced after stimulation with CpG-oligodeoxynucleotide AAC-30, IL-3, or interleukin-3 plus CD40 ligand. Activated pDC responded to ANP with an increase in cGMP production, indicating that GC-A expressed on pDC was functional. We investigated whether tonsillar pDC express GC-A by immunohistochemistry and immunofluorescence staining. We found that GC-A+ HLA-DR+ cells were present in the T-cell areas and the perivascular areas. Flow cytometric analysis with tonsillar cells confirmed that lineage- CD123high pDC express GC-A. These results indicate that the ANP/GC-A system is involved in immune regulation through pDC in secondary lymphoid organs.
AB - Atrial natriuretic peptide is a cardiovascular hormone secreted mainly by the cardiac atria and regulates the volume-pressure homeostasis. The action of ANP is mediated by GC-A.We previously reported that human monocyte-derived dendritic cells express GC-A and respond to ANP with polarization toward a Th2-inducing phenotype. In the present study, we explored the possibility that pDC are subjected to immunoregulation via the ANP/GC-A system.We examined GC-A expression on blood pDC and found that GC-A was not expressed on fresh pDC but was induced after stimulation with CpG-oligodeoxynucleotide AAC-30, IL-3, or interleukin-3 plus CD40 ligand. Activated pDC responded to ANP with an increase in cGMP production, indicating that GC-A expressed on pDC was functional. We investigated whether tonsillar pDC express GC-A by immunohistochemistry and immunofluorescence staining. We found that GC-A+ HLA-DR+ cells were present in the T-cell areas and the perivascular areas. Flow cytometric analysis with tonsillar cells confirmed that lineage- CD123high pDC express GC-A. These results indicate that the ANP/GC-A system is involved in immune regulation through pDC in secondary lymphoid organs.
KW - Atrial natriuretic peptide
KW - Interferon-α
KW - Plasmacytoid dendritic cells
KW - cGMP
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UR - http://www.scopus.com/inward/citedby.url?scp=70149117749&partnerID=8YFLogxK
U2 - 10.1111/j.1348-0421.2009.00149.x
DO - 10.1111/j.1348-0421.2009.00149.x
M3 - Article
C2 - 19563399
AN - SCOPUS:70149117749
SN - 0385-5600
VL - 53
SP - 403
EP - 411
JO - Microbiology and Immunology
JF - Microbiology and Immunology
IS - 7
ER -