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Hif-2α programs oxygen chemosensitivity in chromaffin cells
Maria Prange-Barczynska, … , Thomas P. Keeley, Tammie Bishop
Maria Prange-Barczynska, … , Thomas P. Keeley, Tammie Bishop
Published August 6, 2024
Citation Information: J Clin Invest. 2024;134(18):e174661. https://doi.org/10.1172/JCI174661.
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Research Article Development Oncology

Hif-2α programs oxygen chemosensitivity in chromaffin cells

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Abstract

The study of transcription factors that determine specialized neuronal functions has provided invaluable insights into the physiology of the nervous system. Peripheral chemoreceptors are neurone-like electrophysiologically excitable cells that link the oxygen concentration of arterial blood to the neuronal control of breathing. In the adult, this oxygen chemosensitivity is exemplified by type I cells of the carotid body, and recent work has revealed one isoform of the hypoxia-inducible transcription factor (HIF), HIF-2α, as having a nonredundant role in the development and function of that organ. Here, we show that activation of HIF-2α, including isolated overexpression of HIF-2α but not HIF-1α, is sufficient to induce oxygen chemosensitivity in adult adrenal medulla. This phenotypic change in the adrenal medulla was associated with retention of extra-adrenal paraganglioma-like tissues resembling the fetal organ of Zuckerkandl, which also manifests oxygen chemosensitivity. Acquisition of chemosensitivity was associated with changes in the adrenal medullary expression of gene classes that are ordinarily characteristic of the carotid body, including G protein regulators and atypical subunits of mitochondrial cytochrome oxidase. Overall, the findings suggest that, at least in certain tissues, HIF-2α acts as a phenotypic driver for cells that display oxygen chemosensitivity, thus linking 2 major oxygen-sensing systems.

Authors

Maria Prange-Barczynska, Holly A. Jones, Yoichiro Sugimoto, Xiaotong Cheng, Joanna D.C.C. Lima, Indrika Ratnayaka, Gillian Douglas, Keith J. Buckler, Peter J. Ratcliffe, Thomas P. Keeley, Tammie Bishop

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Figure 1

RNA-Seq of Phd2KO versus WT AM and CBs from young adult mice.

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RNA-Seq of Phd2KO versus WT AM and CBs from young adult mice.
(A) Princi...
(A) Principal component analysis (PCA) of bulk RNA-Seq of CB and AM from Phd2KO and WT mice; RNA was extracted from 5 pairs of approximately 2-month-old animals per biological replicate; n = 3 or 2 biological replicates for CB or AM, respectively. PC1, first principal component; PC2, second principal component. (B) Individual genes that are induced (green) or repressed (purple) by Phd2KO in the AM (absolute value of log2 fold change > log2[1.5] and FDR < 0.1; likelihood ratio test) are overlaid onto genes differentially expressed in WT CB versus WT AM. Gene names are shown for a subset whose mRNA abundance in transcripts per million (TPM) in WT or Phd2KO AM is greater than 10. (C) Data from B shown as a box plot. The fold difference in mRNA abundance in WT CB versus WT AM for genes induced (green) or repressed (purple) by Phd2KO in the AM was compared against that for all other genes (gray) using the 2-sided Mann-Whitney U test. n = 108 (Phd2KO induced); n = 15,032 (others); n = 75 (Phd2KO repressed).

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ISSN: 0021-9738 (print), 1558-8238 (online)

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