# Vhl safeguards thymic epithelial cell identity and thymopoietic capacity by constraining Hif1a activity during development

**Authors:** Christiane Grammer, Julia A. Komorowska, Jeremy B. Swann

PMC · DOI: 10.1016/j.isci.2024.110258 · iScience · 2024-06-13

## TL;DR

This study shows that Vhl helps thymic epithelial cells develop properly by controlling Hif1a activity, even in low-oxygen conditions.

## Contribution

The study reveals a novel role of Vhl in constraining Hif1a activity in thymic epithelial cells under hypoxia.

## Key findings

- Vhl is essential for normal development of mouse thymic epithelial cells.
- Loss of Vhl in TECs causes defects in thymopoiesis, which can be rescued by Hif1a co-depletion.
- Hif1a is not required for TEC development even in hypoxic conditions.

## Abstract

The thymus is a physiologically hypoxic organ and fulfills its role of generating T cells under low-oxygen conditions. We have therefore investigated how thymic epithelial cells (TECs) cope with physiological hypoxia by focusing on the role of the Hif1a–Vhl axis. In most cell types, the oxygen-labile transcriptional regulator Hif1a is a central player in co-ordinating responses to low oxygen: under normoxic conditions Hif1a is rapidly degraded in a Vhl-guided manner; however, under hypoxic conditions Hif1a is stabilized and can execute its transcriptional functions. Unexpectedly, we find that, although TECs reside in a hypoxic microenvironment, they express little Hif1a protein and do not require Hif1a for their development or function. Instead, we find that Vhl function in TECs is vital to constrain Hif1a activity, as loss of Vhl results in dramatic defects in TEC differentiation and thymopoiesis, which can be rescued by Hif1a co-depletion.

•Vhl is required for normal development of mouse thymic epithelial cells•Development of Vhl-deficient TECs can be largely restored by co-depletion of Hif1a•Hif1a-deficient TECs develop normally, even in the low-O2 environment of the thymus

Vhl is required for normal development of mouse thymic epithelial cells

Development of Vhl-deficient TECs can be largely restored by co-depletion of Hif1a

Hif1a-deficient TECs develop normally, even in the low-O2 environment of the thymus

Immunology; Molecular Biology; Molecular Genetics

## Linked entities

- **Genes:** VHL (von Hippel-Lindau tumor suppressor) [NCBI Gene 7428], HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** VHL (von Hippel-Lindau tumor suppressor) [NCBI Gene 7428] {aka HRCA1, RCA1, VHL1, pVHL}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}
- **Diseases:** hypoxia (MESH:D000860), hypoxic (MESH:D002534)
- **Chemicals:** oxygen (MESH:D010100)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11261450/full.md

## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC11261450/full.md

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Source: https://tomesphere.com/paper/PMC11261450