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The findings of association in different populations with different SNPs support a conclusion that variation close to the ANKRA2 (show ANKRA2 Proteins)/CD180 locus analysed in this study contributes to differential response to pathogen exposure.
The role of TLR2, TLR4 (show TLR4 Proteins) and RP105/MD1 (show LY86 Proteins) in the immunoregulatory effect of acidic exopolysaccharides from Lactobacillus plantarum N14 (show CLPTM1 Proteins), is reported.
Silencing Cd180 results in increased phagocytosis while tempering the production of the proinflammatory cytokine TNF (show TNF Proteins) during Borrelia burgdorferi infection.
the close association between the increased proportion of CD180-negative B cells and the activation of IFN-alpha (show IFNA Proteins) signaling in Systemic lupus erythematosus, is reported.
Data show that RP105 (show GPR83 Proteins) knockout (-/-) smooth muscle cells and mast cells secreted higher levels of chemokine (C-C motif) ligand 2 (show CCL2 Proteins) protein (CCL2 (show CCL2 Proteins)).
These data unveil a novel innate immune signaling axis that orchestrates key cytokine responses of macrophages and provide molecular insight into the functions of RP105 (show GPR83 Proteins) as an innate immune receptor for mycobacteria.
RP105 (show GPR83 Proteins) regulates monocyte-driven arteriogenesis in a murine hind limb ischemia model.
RP105 deficiency results in reduced early atherosclerotic plaque development with a marked decrease in lesional macrophage content, which may be due to disturbed migration of RP105 deficient monocytes resulting from CCR2 downregulation
Deficiency of the endogenous TLR4 (show TLR4 Proteins) inhibitor, RP105 (show GPR83 Proteins), leads to pronounced cardiac dilation after myocardial infarction.
Data indicate that RP105 (show GPR83 Proteins) and TLR4 (show TLR4 Proteins) are both expressed by vascular smooth muscle cells (VSMC).
RP105 (show GPR83 Proteins) deficiency on circulating cells results in an intriguing unexpected TLR-associated mechanisms that decrease atherosclerotic lesion formation with alterations on proinflammatory B2 B cells.
The function of TLR2 and TLR4 (show TLR4 Proteins) in response to TLR ligands could be associated with each other by RP105 (show GPR83 Proteins).
Calcitriol regulates immune genes CD14 (show NDUFA2 Proteins) and CD180 to modulate LPS (show IRF6 Proteins) responses in human trophoblasts.
CD150 (show SLAMF1 Proteins) and CD180 receptors may modulate transcriptional program in lymphocytic leukemia cells by regulating the transcription factor expression levels
Our data strongly support the use of CCR2 (show CCR2 Proteins) and CD180 mRNAs as whole blood pharmacodynamic (PD)biomarkers for BRD4 (show BRD4 Proteins) inhibitors, especially in situations where paired tumor biopsies are unavailable. In addition, they can be used as tumor-based PD biomarkers for hematologic tumors.
combination of signals via CD150 (show SLAMF1 Proteins) and CD180 leads to blocking of pro-survival pathways that may be a restraining factor for neoplastic CLL B cells propagation in more than 50% of CLL cases where these receptors are coexpressed
CD180 expression is significantly upregulated in human masticatory mucosa during wound healing
By associating with PIM (show PIM1 Proteins)-1L, CD180 can thus obtain autonomous signaling capabilities, and this complex is then channeling inflammatory signals into B cell survival programs
Since MEC1 cells are derived from a CLL patient with mutated IGVH genes (M-CLL) negative correlation between CD180 and CD32 expression on cycling MEC1 cells could be limited to M-CLL.
we address of monocytes functional status through assessment of the patterns of expression of Fcgamma receptors CD64 (show FCGR1A Proteins), CD32, CD16 (show CD16 Proteins) and CD180 receptor on monocytes from CLL patients and healthy individuals using specific mAbs and flow cytometry.
CD180 is a cell surface molecule consisting of extracellular leucine-rich repeats (LRR) and a short cytoplasmic tail. The extracellular LRR is associated with a molecule called MD-1 and form the cell surface receptor complex, RP105/MD-1. It belongs to the family of pathogen receptors, Toll-like receptors (TLR). RP105/MD1, by working in concert with TLR4, controls B cell recognition and signaling of lipopolysaccharide (LPS), a membrane constituent of Gram-negative bacteria.
, lymphocyte antigen 78
, CD180 molecule
, radio protective 105
, lymphocyte antigen 64-like protein
, radioprotective 105 kDa protein
, lymphocyte antigen 64
, lymphocyte antigen-64, radioprotective, 105kDa