Hypoxia and Inflammation: Insights From High-Altitude Physiology

The key regulators of the transcriptional response to hypoxia and inflammation (hypoxia inducible factor, HIF, and nuclear factor-kappa B, NF-κB, respectively) are evolutionarily conserved and share significant crosstalk. Tissues often experience hypoxia and inflammation concurrently at the site of...

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Main Authors: Kathy Pham, Keval Parikh, Erica C. Heinrich
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2021.676782/full
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spelling doaj-ec8ba9dc096746b4bde9ce2c7fd8fd152021-05-26T13:18:30ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2021-05-011210.3389/fphys.2021.676782676782Hypoxia and Inflammation: Insights From High-Altitude PhysiologyKathy PhamKeval ParikhErica C. HeinrichThe key regulators of the transcriptional response to hypoxia and inflammation (hypoxia inducible factor, HIF, and nuclear factor-kappa B, NF-κB, respectively) are evolutionarily conserved and share significant crosstalk. Tissues often experience hypoxia and inflammation concurrently at the site of infection or injury due to fluid retention and immune cell recruitment that ultimately reduces the rate of oxygen delivery to tissues. Inflammation can induce activity of HIF-pathway genes, and hypoxia may modulate inflammatory signaling. While it is clear that these molecular pathways function in concert, the physiological consequences of hypoxia-induced inflammation and how hypoxia modulates inflammatory signaling and immune function are not well established. In this review, we summarize known mechanisms of HIF and NF-κB crosstalk and highlight the physiological consequences that can arise from maladaptive hypoxia-induced inflammation. Finally, we discuss what can be learned about adaptive regulation of inflammation under chronic hypoxia by examining adaptive and maladaptive inflammatory phenotypes observed in human populations at high altitude. We aim to provide insight into the time domains of hypoxia-induced inflammation and highlight the importance of hypoxia-induced inflammatory sensitization in immune function, pathologies, and environmental adaptation.https://www.frontiersin.org/articles/10.3389/fphys.2021.676782/fullhypoxiainflammationhigh altitudehypoxia inducible factornuclear factor-κB
collection DOAJ
language English
format Article
sources DOAJ
author Kathy Pham
Keval Parikh
Erica C. Heinrich
spellingShingle Kathy Pham
Keval Parikh
Erica C. Heinrich
Hypoxia and Inflammation: Insights From High-Altitude Physiology
Frontiers in Physiology
hypoxia
inflammation
high altitude
hypoxia inducible factor
nuclear factor-κB
author_facet Kathy Pham
Keval Parikh
Erica C. Heinrich
author_sort Kathy Pham
title Hypoxia and Inflammation: Insights From High-Altitude Physiology
title_short Hypoxia and Inflammation: Insights From High-Altitude Physiology
title_full Hypoxia and Inflammation: Insights From High-Altitude Physiology
title_fullStr Hypoxia and Inflammation: Insights From High-Altitude Physiology
title_full_unstemmed Hypoxia and Inflammation: Insights From High-Altitude Physiology
title_sort hypoxia and inflammation: insights from high-altitude physiology
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2021-05-01
description The key regulators of the transcriptional response to hypoxia and inflammation (hypoxia inducible factor, HIF, and nuclear factor-kappa B, NF-κB, respectively) are evolutionarily conserved and share significant crosstalk. Tissues often experience hypoxia and inflammation concurrently at the site of infection or injury due to fluid retention and immune cell recruitment that ultimately reduces the rate of oxygen delivery to tissues. Inflammation can induce activity of HIF-pathway genes, and hypoxia may modulate inflammatory signaling. While it is clear that these molecular pathways function in concert, the physiological consequences of hypoxia-induced inflammation and how hypoxia modulates inflammatory signaling and immune function are not well established. In this review, we summarize known mechanisms of HIF and NF-κB crosstalk and highlight the physiological consequences that can arise from maladaptive hypoxia-induced inflammation. Finally, we discuss what can be learned about adaptive regulation of inflammation under chronic hypoxia by examining adaptive and maladaptive inflammatory phenotypes observed in human populations at high altitude. We aim to provide insight into the time domains of hypoxia-induced inflammation and highlight the importance of hypoxia-induced inflammatory sensitization in immune function, pathologies, and environmental adaptation.
topic hypoxia
inflammation
high altitude
hypoxia inducible factor
nuclear factor-κB
url https://www.frontiersin.org/articles/10.3389/fphys.2021.676782/full
work_keys_str_mv AT kathypham hypoxiaandinflammationinsightsfromhighaltitudephysiology
AT kevalparikh hypoxiaandinflammationinsightsfromhighaltitudephysiology
AT ericacheinrich hypoxiaandinflammationinsightsfromhighaltitudephysiology
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