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Updated: Jan 28, 2026

Measuring Mitochondrial Function of Naïve and Effector CD8 T Cells
Published on: March 28, 2025
Expression of the Phosphatase Ppef2 Controls Survival and Function of CD8+ Dendritic Cells
Markus Zwick1, Thomas Ulas2, Yi-Li Cho3
1Faculty of Medicine, Biomedical Center (BMC), Institute for Immunology, LMU Munich, Planegg-Martinsried, Germany.
Abstract:
Apoptotic cell death of Dendritic cells (DCs) is critical for immune homeostasis. Although intrinsic mechanisms controlling DC death have not been fully characterized up to now, experimentally enforced inhibition of DC-death causes various autoimmune diseases in model systems. We have generated mice deficient for Protein Phosphatase with EF-Hands 2 (Ppef2), which is selectively expressed in CD8+ DCs, but not in other related DC subtypes such as tissue CD103+ DCs. Ppef2 is down-regulated rapidly upon maturation of DCs by toll-like receptor stimuli, but not upon triggering of CD40. Ppef2-deficient CD8+ DCs accumulate the pro-apoptotic Bcl-2-like protein 11 (Bim) and show increased apoptosis and reduced competitve repopulation capacities. Furthermore, Ppef2-/- CD8+ DCs have strongly diminished antigen presentation capacities in vivo, as CD8+ T cells primed by Ppef2-/- CD8+ DCs undergo reduced expansion. In conclusion, our data suggests that Ppef2 is crucial to support survival of immature CD8+ DCs, while Ppef2 down-regulation during DC-maturation limits T cell responses.
Insights
Protein Phosphatase with EF-Hands 2 (Ppef2) is essential for maintaining immature CD8+ dendritic cell survival. Its down-regulation during maturation limits T cell responses, impacting immune homeostasis.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Apoptotic cell death in dendritic cells (DCs) is vital for immune homeostasis.
- Dysregulation of DC death can lead to autoimmune diseases.
- Mechanisms controlling DC apoptosis are not fully understood.
Purpose of the Study:
- To investigate the role of Protein Phosphatase with EF-Hands 2 (Ppef2) in CD8+ dendritic cell survival and function.
- To elucidate the impact of Ppef2 deficiency on DC apoptosis and T cell priming.
Main Methods:
- Generation and analysis of Ppef2-deficient mice.
- Flow cytometry to assess DC apoptosis and Bim accumulation.
- In vivo studies to evaluate antigen presentation and T cell expansion.
Main Results:
- Ppef2 is selectively expressed in CD8+ DCs and down-regulated upon maturation.
- Ppef2 deficiency leads to increased CD8+ DC apoptosis due to Bim accumulation.
- Ppef2-deficient CD8+ DCs exhibit impaired antigen presentation and reduced CD8+ T cell expansion.
Conclusions:
- Ppef2 is crucial for the survival of immature CD8+ DCs.
- Ppef2 down-regulation during DC maturation regulates T cell responses.
- Ppef2 plays a significant role in immune homeostasis by controlling CD8+ DC apoptosis.
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