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http://purl.uniprot.org/citations/30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30924074http://www.w3.org/2000/01/rdf-schema#comment"Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder with no cure, and elucidation of the mechanisms mediating neuronal death in this neuropathology is crucial to develop effective treatments. It has recently been demonstrated in animal models that the Wnt family of proteins is involved in this neuropathology, although its potential involvement in case of humans is almost unknown. We analyzed the expression of Wnt signaling components in healthy and ALS human spinal cords by quantitative RT-PCR, and we found that most Wnt ligands, modulators, receptors, and co-receptors were expressed in healthy controls. Moreover, we observed clear alterations in the mRNA expression of different components of this family of proteins in human spinal cord tissue from ALS cases. Specifically, we detected a significant increase in the mRNA levels of Wnt3, Wnt4, Fz2, and Fz8, together with several non-significant increases in the mRNA expression of other genes such as Wnt2b, Wnt5a, Fz3, Lrp5, and sFRP3. Based on these observations and on previous reports of studies performed in animal models, we evaluated with immunohistochemistry the protein expression patterns of Fz2 and Fz5 receptors and their main ligand Wnt5a in control samples and ALS cases. No substantial changes were observed in Fz5 protein expression pattern in ALS samples. However, we detected an increase in the amount of Fz2+ astrocytes in the borderline between gray and white matter at the ventral horn in ALS samples. Finally, Wnt5a expression was observed in neurons and astrocytes in both control and ALS samples, although Wnt5a immunolabeling in astroglial cells was significantly increased in ALS spinal cords in the same region where changes in Fz2 were observed. Altogether, these observations strongly suggest that the Wnt family of proteins, and more specifically Fz2 and Wnt5a, might be involved in human ALS pathology."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.org/dc/terms/identifier"doi:10.1007/s12035-019-1547-9"xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/author"Gonzalez P."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/author"Ferrer I."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/author"Rodriguez F.J."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/author"Andres-Benito P."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/author"Gonzalez-Fernandez C."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/name"Mol Neurobiol"xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/pages"6777-6791"xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/title"Wnt Signaling Alterations in the Human Spinal Cord of Amyotrophic Lateral Sclerosis Cases: Spotlight on Fz2 and Wnt5a."xsd:string
http://purl.uniprot.org/citations/30924074http://purl.uniprot.org/core/volume"56"xsd:string
http://purl.uniprot.org/citations/30924074http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/30924074
http://purl.uniprot.org/citations/30924074http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/30924074
http://purl.uniprot.org/uniprot/#_A0A384N611-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/#_A0FKN4-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/#_B3KQX9-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/#_P41221-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/#_Q14332-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/#_Q86UZ8-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/#_Q6DK41-mappedCitation-30924074http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/A0FKN4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/Q14332http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30924074
http://purl.uniprot.org/uniprot/B3KQX9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30924074