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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002218naa a2200325 4500
001oai:prod.swepub.kib.ki.se:138152944
003SwePub
008240701s2018 | |||||||||||000 ||eng|
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1381529442 URI
024a https://doi.org/10.7554/elife.346812 DOI
040 a (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Macias, D4 aut
2451 0a HIF-2α is essential for carotid body development and function
264 c 2018-04-19
264 1b eLife Sciences Publications, Ltd,c 2018
520 a Mammalian adaptation to oxygen flux occurs at many levels, from shifts in cellular metabolism to physiological adaptations facilitated by the sympathetic nervous system and carotid body (CB). Interactions between differing forms of adaptive response to hypoxia, including transcriptional responses orchestrated by the Hypoxia Inducible transcription Factors (HIFs), are complex and clearly synergistic. We show here that there is an absolute developmental requirement for HIF-2α, one of the HIF isoforms, for growth and survival of oxygen sensitive glomus cells of the carotid body. The loss of these cells renders mice incapable of ventilatory responses to hypoxia, and this has striking effects on processes as diverse as arterial pressure regulation, exercise performance, and glucose homeostasis. We show that the expansion of the glomus cells is correlated with mTORC1 activation, and is functionally inhibited by rapamycin treatment. These findings demonstrate the central role played by HIF-2α in carotid body development, growth and function.
700a Cowburn, AS4 aut
700a Torres-Torrelo, H4 aut
700a Ortega-Saenz, P4 aut
700a Lopez-Barneo, J4 aut
700a Johnson, RSu Karolinska Institutet4 aut
710a Karolinska Institutet4 org
773t eLifed : eLife Sciences Publications, Ltdg 7q 7x 2050-084X
856u https://doi.org/10.7554/elife.34681
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:138152944
8564 8u https://doi.org/10.7554/elife.34681

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