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Ccr7 functions during axis formation as a GPCR to inhibit beta-catenin (show CTNNB1 Proteins), likely by promoting Ca(2 (show CA2 Proteins)+) transients throughout the blastula.
Data report that CCR7 mediates CD11c (show ITGAX Proteins)+ cell migration from the CNS parenchyma to the meningeal lymphoid vessels and eventually to the deep cervical lymph nodes during neuroinflammation. In the absence of CCR7, dendritic cells are retained in the CNS and exacerbate neuroinflammation.
Conditions for optimal dendritic cells guidance are perfectly provided by the CCL21 (show CCL21 Proteins) gradients measured in vivo. Furthermore, CCR7 signal termination by the G-protein-coupled receptor kinase 6 (GRK6 (show GRK6 Proteins)) is crucial for haptotactic but dispensable for chemotactic CCL21 (show CCL21 Proteins) gradient sensing in vitro and confirm those observations in vivo.
CCR7 deficiency results in apoptosis of Sirpa (show SIRPA Proteins)- dendritic cells, which is counterbalanced by expansion of immature Sirpa (show SIRPA Proteins)+ dendritic cells that efficiently induce Treg generation.
These data show that CCR7-CCL19 (show CCL19 Proteins)/CCL21 (show CCL21 Proteins) axis facilitates retention CD4 (show CD4 Proteins)(+) T lymphocytes at the site of collateral artery remodeling, which is essential for effective arteriogenesis.
Results demonstrated that the deletion of CCR7 significantly decreases levels of activated Notch1 (show NOTCH1 Proteins), and provide evidence that crosstalk between CCR7 and Notch1 (show NOTCH1 Proteins) promotes stemness in mammary cancer cells ultimately potentiating mammary tumor progression.
CCR7 deficiency lead to accumulation of CD8 (show CD8A Proteins)+ adipose tissue leukocytes, which was further exacerbated by HFD feeding.
in the current study, we used interval mapping to validate a locus on Chr 15, named Ity8, linked to Salmonella resistance in AcB60 mice. Global gene expression analysis during infection identified AcB60-specific expression of genes involved in Ccr7 signaling, including downstream effector Mapk11 (mitogen-activated protein kinase 11 (show MAPK11 Proteins)), located within the Ity8 interval, and representing a potential positional candidate gene
Taken together, these data suggest that CCR7 biases memory CD8 (show CD8A Proteins) T cells toward IL-7 (show IL7 Proteins)-dependent niches over IL-15 (show IL15 Proteins)-dependent niches, which provides insight into the homeostatic regulation of different memory T-cell subsets.
Prominent mucosal immune responses in CCR7-deficient mice increased the efficiency of bacteria clearance from the FRT(female reproductive tract) while reducing tissue-associated inflammation and pathology; increased numbers of lymphocytes within the FRT result in pathogen clearance with reduced immune-mediated pathology
CCR7 is required to mount a robust immune response against enteropathogenic Y. pseudotuberculosis by promoting Th17-like responses in mesenteric lymph nodes.
High CCR7 expression is associated with urinary bladder cancer metastasis.
these data indicate CCL19 (show CCL19 Proteins)/CCR7 contributes to proliferation and invasion of ESCs (show NR2E3 Proteins), which are conducive to the pathogenesis of endometriosis through activating PI3K (show PIK3CA Proteins)/Akt (show AKT1 Proteins) pathway
The research findings demonstrate for the first time that the chemokines CCL19 (show CCL19 Proteins), CCL21 (show CCL21 Proteins) and CCR7 play important roles in bone destruction by increasing osteoclast migration and resorption activity, and that has been linked to rheumatoid arthritis pathogenesis.
CXCR4 (show CXCR4 Proteins), CCR7, VEGF-C (show VEGFC Proteins) and VEGF-D (show Figf Proteins) expression might have synergistic effects on the lymph node metastasis in patients with cervical cancer.
the acute GvHD (aGvHD) patients received higher percentage of CD4 (show CD4 Proteins)+CCR7+ T-cells in donor T-cells, whereas chronic GvHD (cGvHD) patients were transplanted with higher percentages of CD8 (show CD8A Proteins)+CCR7+ T-cells. Functional experiments demonstrated that CCR7+ T-cells exhibited higher potential for activation than CCR7- T-cells did.
these results demonstrated that CCL21/CCR7 may activate EMT in lung cancer cells via the ERK1/2 signaling pathway.
CCL21 (show CCL21 Proteins)/CCR7 interaction was shown to allow NK cell adhesion to endothelial cells (ECs) and its reduction by hypoxia.
Study shows that miR (show MLXIP Proteins)-1275 can positively regulate CCR7 expression in squamous cell carcinoma of head and neck (SCCHN) with different mechanisms.
Study provide evidence that CCR7 mediates EMT (show ITK Proteins) progress via AKT (show AKT1 Proteins) pathway, which indicates that CCR7 has a key role in breast cancer progression.
Report an increased percentage of peripheral CCR7 T cells accompanied by endothelial dysfunction in patients with ankylosing spondylitis.
Fluorescent dye-labeled gammadelta T cells from afferent and efferent lymph lack CCR7 surface expression and display high levels of CD62L (show SELL Proteins) compared with CD4 (show CD4 Proteins) T cells, which do express CCR7.
CCR7 transcripts were minimally expressed in ex vivo and proliferating WC1(+)gammadelta T cells, a unique cell population with proinflammatory characteristics
the pattern of expression of CCR7 in different populations of porcine lymphocytes appears to be similar to that of human, highlighting the value of the pig as a useful animal model for biomedical studies.
Pre-translntation of sertli cell CCR7 significantly suppresses lymphocyte proliferation and prolongs allogeneic skin graft survival.
The protein encoded by this gene is a member of the G protein-coupled receptor family. This receptor was identified as a gene induced by the Epstein-Barr virus (EBV), and is thought to be a mediator of EBV effects on B lymphocytes. This receptor is expressed in various lymphoid tissues and activates B and T lymphocytes. It has been shown to control the migration of memory T cells to inflamed tissues, as well as stimulate dendritic cell maturation. The chemokine (C-C motif) ligand 19 (CCL19/ECL) has been reported to be a specific ligand of this receptor.
C-C chemokine receptor type 7
, CC chemokine receptor 7
, chemokine (C-C motif) receptor 7 a
, chemokine (C-C motif) receptor 7
, c-C chemokine receptor type 7-like
, C-C CKR-7
, EBV-induced G-protein coupled receptor 1
, MIP-3 beta receptor
, chemokine (C-C) receptor 7
, epstein-Barr virus-induced G-protein coupled receptor 1
, EBV-induced G protein-coupled receptor 1
, Epstein-Barr virus induced G-protein coupled receptor
, Epstein-Barr virus induced gene 1
, lymphocyte-specific G protein-coupled peptide receptor
, chemokine receptor 7