S100B and S100A6 differentially modulate cell survival by interacting with distinct RAGE (receptor for advanced glycation end products) immunoglobulin domains (Q24338574)

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English	S100B and S100A6 differentially modulate cell survival by interacting with distinct RAGE (receptor for advanced glycation end products) immunoglobulin domains	scientific article

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scholarly article

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S100B and S100A6 differentially modulate cell survival by interacting with distinct RAGE (receptor for advanced glycation end products) immunoglobulin domains (English)

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author name string

Estelle Leclerc

1

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Günter Fritz

2

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Mirjam Weibel

3

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Claus W Heizmann

4

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Arnaud Galichet

5

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language of work or name

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publication date

26 October 2007

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Journal of Biological Chemistry

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282

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31317-31

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43

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Calcium-dependent and -independent interactions of the S100 protein family.

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S100B in brain damage and neurodegeneration

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S100A12 protein is a strong inducer of neurite outgrowth from primary hippocampal neurons.

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Active secretion of S100B from astrocytes during metabolic stress.

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Spatial and temporal expression of S100B in cells of oligodendrocyte lineage

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Evidence for a wide extra-astrocytic distribution of S100B in human brain

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Production and characterization of monoclonal antibodies with specificity for the S100 beta polypeptide of brain S100 fractions

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Secretion of S-100 from rat C6 glioma cells.

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Distribution of a specific calcium-binding protein of the S100 protein family, S100A6 (calcyclin), in subpopulations of neurons and glial cells of the adult rat nervous system.

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Selective association of S100A6 (calcyclin)-immunoreactive astrocytes with the tangential migration pathway of subventricular zone cells in the rat.

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Differential expression of S100B and S100A6(1) in the human fetal and aged cerebral cortex.

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S100A6 overexpression within astrocytes associated with impaired axons from both ALS mouse model and human patients

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The extracellular region of the receptor for advanced glycation end products is composed of two independent structural units.

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RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides

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Structural and functional insights into RAGE activation by multimeric S100B

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Splice variants of the receptor for advanced glycosylation end products (RAGE) in human brain

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cDNA cloning of a novel secreted isoform of the human receptor for advanced glycation end products and characterization of cells co-expressing cell-surface scavenger receptors and Swedish mutant amyloid precursor protein.

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The biology of the receptor for advanced glycation end products and its ligands

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S100 protein translocation in response to extracellular S100 is mediated by receptor for advanced glycation endproducts in human endothelial cells

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Expression and purification of the soluble isoform of human receptor for advanced glycation end products (sRAGE) from Pichia pastoris.

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Immobilized prion protein undergoes spontaneous rearrangement to a conformation having features in common with the infectious form

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Characterization of presenilin complexes from mouse and human brain using Blue Native gel electrophoresis reveals high expression in embryonic brain and minimal change in complex mobility with pathogenic presenilin mutations

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S100B protects LAN-5 neuroblastoma cells against Abeta amyloid-induced neurotoxicity via RAGE engagement at low doses but increases Abeta amyloid neurotoxicity at high doses

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Receptor for advanced glycation end products (RAGE)-mediated neurite outgrowth and activation of NF-kappaB require the cytoplasmic domain of the receptor but different downstream signaling pathways

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S100B inhibits myogenic differentiation and myotube formation in a RAGE-independent manner

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Amphoterin stimulates myogenesis and counteracts the antimyogenic factors basic fibroblast growth factor and S100B via RAGE binding

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Receptor for advanced glycation end products plays a more important role in cellular survival than in neurite outgrowth during retinoic acid-induced differentiation of neuroblastoma cells

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Receptor for advanced glycation end products (RAGE) signaling induces CREB-dependent chromogranin expression during neuronal differentiation

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RAGE and amyloid-beta peptide neurotoxicity in Alzheimer's disease

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N(epsilon)-(carboxymethyl)lysine adducts of proteins are ligands for receptor for advanced glycation end products that activate cell signaling pathways and modulate gene expression

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Astrocytosis and axonal proliferation in the hippocampus of S100b transgenic mice

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Neurotrophic protein S100 beta stimulates glial cell proliferation

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The receptor for advanced glycation end products (RAGE) is a cellular binding site for amphoterin. Mediation of neurite outgrowth and co-expression of rage and amphoterin in the developing nervous system

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Transgenic mice overexpressing the neurotrophic factor S-100 beta show neuronal cytoskeletal and behavioral signs of altered aging processes: implications for Alzheimer's disease and Down's syndrome.

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Immunohistochemical distribution of the receptor for advanced glycation end products in neurons and astrocytes in Alzheimer's disease.

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Increased susceptibility of S100B transgenic mice to perinatal hypoxia-ischemia.

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Proteins of the brain extracellular fluid: evidence for release of S-100 protein.

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RAGE potentiates Abeta-induced perturbation of neuronal function in transgenic mice

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S100B-stimulated NO production by BV-2 microglia is independent of RAGE transducing activity but dependent on RAGE extracellular domain

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Astrocytic calcium/zinc binding protein S100A6 over expression in Alzheimer's disease and in PS1/APP transgenic mice models

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Blockade of RAGE–amphoterin signalling suppresses tumour growth and metastases

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S100A6, a calcium- and zinc-binding protein, is overexpressed in SOD1 mutant mice, a model for amyotrophic lateral sclerosis

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Global analysis of a macromolecular interaction measured on BIAcore

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7 January 2021

based on heuristic

inferred from DOI database lookup

Coregulation of neurite outgrowth and cell survival by amphoterin and S100 proteins through receptor for advanced glycation end products (RAGE) activation

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https://api.crossref.org/works/10.1074%2FJBC.M703951200

7 January 2021

based on heuristic

inferred from DOI database lookup

Hexameric calgranulin C (S100A12) binds to the receptor for advanced glycated end products (RAGE) using symmetric hydrophobic target-binding patches

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M703951200

7 January 2021

based on heuristic

inferred from DOI database lookup

Cell-specific expression of high levels of human S100 beta in transgenic mouse brain is dependent on gene dosage

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1074/JBC.M703951200

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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