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Cited by 187

The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.

Abnormal Sympathoadrenal Development and Systemic Hypotension in PHD3−/− Mice

Open access
Bishop, Tammie, Gallagher, Denis, Pascual, Alberto, Lygate, Craig A., de Bono, Joseph P., Nicholls, Lynn G., Ortega-Saenz, Patricia, Oster, Henrik, Wijeyekoon, Bhathiya, Sutherland, Andrew I., Grosfeld, Alexandra, Aragones, Julian, Schneider, Martin, van Geyte, Katie, Teixeira, Dania, Diez-Juan, Antonio, Lopez-Barneo, Jose, Channon, Keith M., Maxwell, Patrick H., Pugh, Christopher W., Davies, Alun M., Carmeliet, Peter, Ratcliffe, Peter J.·2008·Molecular and Cellular Biology

Abstract

Cell culture studies have implicated the oxygen-sensitive hypoxia-inducible factor (HIF) prolyl hydroxylase PHD3 in the regulation of neuronal apoptosis. To better understand this function in vivo, we have created PHD3(-/-) mice and analyzed the neuronal phenotype. Reduced apoptosis in superior cervical ganglion (SCG) neurons cultured from PHD3(-/-) mice is associated with an increase in the number of cells in the SCG, as well as in the adrenal medulla and carotid body. Genetic analysis by intercrossing PHD3(-/-) mice with HIF-1a(+/-) and HIF-2a(+/-) mice demonstrated an interaction with HIF-2alpha but not HIF-1alpha, supporting the nonredundant involvement of a PHD3-HIF-2alpha pathway in the regulation of sympathoadrenal development. Despite the increased number of cells, the sympathoadrenal system appeared hypofunctional in PHD3(-/-) mice, with reduced target tissue innervation, adrenal medullary secretory capacity, sympathoadrenal responses, and systemic blood pressure. These observations suggest that the role of PHD3 in sympathoadrenal development extends beyond simple control of cell survival and organ mass, with functional PHD3 being required for proper anatomical and physiological integrity of the system. Perturbation of this interface between developmental and adaptive signaling by hypoxic, metabolic, or other stresses could have important effects on key sympathoadrenal functions, such as blood pressure regulation.

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Metadata

Authors
Bishop, T., Gallagher, D., Pascual, A., Lygate, C. A., de Bono, J. P., Nicholls, L. G., Ortega-Saenz, P., Oster, H., Wijeyekoon, B., Sutherland, A. I., Grosfeld, A., Aragones, J., Schneider, M., van Geyte, K., Teixeira, D., Diez-Juan, A., Lopez-Barneo, J., Channon, K. M., Maxwell, P. H., Pugh, C. W., Davies, A. M., Carmeliet, P., & Ratcliffe, P. J.
Venue
Molecular and Cellular Biology
Published
2008-05-01
Volume
28
Issue
10
Pages
3386-3400
ISSN
  • 0270-7306 (ISSN-L)
  • 1098-5549
OpenAlex
W2147891751
Cited by
187
References
13
FWCI
8.93
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Abnormal Sympathoadrenal Development and Systemic Hypotension in PHD3−/− Mice. https://app.cochat.ai/papers/10.1128/mcb.02041-07
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Bishop, T., Gallagher, D., Pascual, A., Lygate, C. A., de Bono, J. P., Nicholls, L. G., Ortega-Saenz, P., Oster, H., Wijeyekoon, B., Sutherland, A. I., Grosfeld, A., Aragones, J., Schneider, M., van Geyte, K., Teixeira, D., Diez-Juan, A., Lopez-Barneo, J., Channon, K. M., Maxwell, P. H., . . . Ratcliffe, P. J. (2008). Abnormal Sympathoadrenal Development and Systemic Hypotension in PHD3−/− Mice. Molecular and Cellular Biology. https://doi.org/10.1128/mcb.02041-07

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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