dc.creatorUrsem, Stan R.
dc.creatorDiepenbroek, Charlene
dc.creatorBacic, Vesna
dc.creatorUnmehopa, Unga A.
dc.creatorEggels, Leslie
dc.creatorMonteiro, Clarissa M. Maya
dc.creatorHeijboer, Annemieke C.
dc.creatorla Fleur, Susanne E.
dc.date2021-08-02T20:17:58Z
dc.date2021-08-02T20:17:58Z
dc.date2021
dc.date.accessioned2023-09-26T22:25:33Z
dc.date.available2023-09-26T22:25:33Z
dc.identifierURSEM, Stan R. et al. Localization of fibroblast growth factor 23 protein in the rat hypothalamus. European Journal of Neuroscience, v. 1, n. 11, 11 p, 2021.
dc.identifier0953-816X
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/48479
dc.identifier10.1111/ejn.15375
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8879043
dc.descriptionFibroblast growth factor 23 (FGF23) is an endocrine growth factor and known to play a pivotal role in phosphate homeostasis. Interestingly, several studies point towards a function of FGF23 in the hypothalamus. FGF23 clas sically activates the FGF receptor 1 in the presence of the co-receptor αKlotho, of both gene expression in the brain was previously established. However, studies on gene and protein expression of FGF23 in the brain are scarce and have been inconsistent. Therefore, our aim was to localise FGF23 gene and protein expression in the rat brain with focus on the hypothalamus. Also, we investigated the protein expression of αKlotho. Adult rat brains were used to localise and visualise FGF23 and αKlotho protein in the hypo thalamus by immunofluorescence labelling. Furthermore, western blots were used for assessing hypothalamic FGF23 protein expression. FGF23 gene expression was investigated by qPCR in punches of the arcuate nucleus, lat eral hypothalamus, paraventricular nucleus, choroid plexus, ventrolateral thalamic nucleus and the ventromedial hypothalamus. Immunoreactivity for FGF23 and αKlotho protein was found in the hypothalamus, third ventricle lining and the choroid plexus. Western blot analysis of the hypothalamus Fibroblast growth factor 23 (FGF23) is an endocrine growth factor and known to play a pivotal role in phosphate homeostasis. Interestingly, several studies point towards a function of FGF23 in the hypothalamus. FGF23 clas sically activates the FGF receptor 1 in the presence of the co-receptor αKlotho, of both gene expression in the brain was previously established. However, studies on gene and protein expression of FGF23 in the brain are scarce and have been inconsistent. Therefore, our aim was to localise FGF23 gene and protein expression in the rat brain with focus on the hypothalamus. Also, we investigated the protein expression of αKlotho. Adult rat brains were used to localise and visualise FGF23 and αKlotho protein in the hypo thalamus by immunofluorescence labelling. Furthermore, western blots were used for assessing hypothalamic FGF23 protein expression. FGF23 gene expression was investigated by qPCR in punches of the arcuate nucleus, lat eral hypothalamus, paraventricular nucleus, choroid plexus, ventrolateral thalamic nucleus and the ventromedial hypothalamus. Immunoreactivity for FGF23 and αKlotho protein was found in the hypothalamus, third ventricle lining and the choroid plexus. Western blot analysis of the hypothalamusFibroblast growth factor 23 (FGF23) is an endocrine growth factor and known to play a pivotal role in phosphate homeostasis. Interestingly, several studies point towards a function of FGF23 in the hypothalamus. FGF23 clas sically activates the FGF receptor 1 in the presence of the co-receptor αKlotho, of both gene expression in the brain was previously established. However, studies on gene and protein expression of FGF23 in the brain are scarce and have been inconsistent. Therefore, our aim was to localise FGF23 gene and protein expression in the rat brain with focus on the hypothalamus. Also, we investigated the protein expression of αKlotho. Adult rat brains were used to localise and visualise FGF23 and αKlotho protein in the hypo thalamus by immunofluorescence labelling. Furthermore, western blots were used for assessing hypothalamic FGF23 protein expression. FGF23 gene expression was investigated by qPCR in punches of the arcuate nucleus, lat eral hypothalamus, paraventricular nucleus, choroid plexus, ventrolateral thalamic nucleus and the ventromedial hypothalamus. Immunoreactivity for FGF23 and αKlotho protein was found in the hypothalamus, third ventricle lining and the choroid plexus. Western blot analysis of the hypothalamusconfirmed the presence of FGF23. Gene expression of FGF23 was not detected, suggesting that the observed FGF23 protein is not brain-derived. Several FGF receptors are known to be present in the brain. Therefore, we conclude that the machinery for FGF23 signal transduction is present in sev eral brain areas, indeed suggesting a role for FGF23 in the brain.
dc.formatapplication/pdf
dc.languageeng
dc.publisherWiley
dc.rightsopen access
dc.subjectHipotálamo
dc.subjectFator de crescimento do fibroblasto 23
dc.subjectTerceiro ventrículo
dc.subjectKlotho
dc.subjectFGF23
dc.subjectFGF23
dc.subjectFibroblast growth factor 23
dc.subjectHypothalamus
dc.subjectKlotho
dc.subjectThird ventricle
dc.subjectTerceiro Ventrículo
dc.titleLocalization of fibroblast growth factor 23 protein in the rat hypothalamus
dc.typeArticle


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