# The Serine/Threonine Kinase NDR2 Regulates Integrin Signaling, Synapse Formation, and Synaptic Plasticity in the Hippocampus

**Authors:** Miguel del Ángel, Atsuhiro Tsutiya, Hussam Hayani, Deniz Madencioglu, Emre Kul, Gürsel Caliskan, Yunus Emre Demiray, Alexander Dityatev, Oliver Stork

PMC · DOI: 10.1111/jnc.70094 · Journal of Neurochemistry · 2025-05-29

## TL;DR

This study shows that the NDR2 kinase helps regulate synapse formation and plasticity in the hippocampus through integrin signaling.

## Contribution

The study reveals a novel role for NDR2 in integrin-dependent synaptic plasticity and memory.

## Key findings

- Ndr2 deficiency reduces phosphorylated β1 integrin at synapses in the hippocampus.
- Ndr2 deficiency leads to decreased synaptic density and impaired long-term potentiation.
- Integrin activation can restore plasticity in Ndr2-deficient mice.

## Abstract

Nuclear Dbf2‐related (NDR) kinases are core components of the Hippo pathway, which controls neuronal polarity and neurite growth in the central nervous system (CNS). NDR2 is the principal NDR kinase in the mouse CNS, where it has been shown to regulate integrin‐dependent dendritic branching as well as growth and plasticity in hippocampal mossy fibers. Given the well‐established involvement of integrins in plasticity, we hypothesized that NDR2 might regulate synapse formation and plasticity through integrin‐mediated mechanisms. In this study, using constitutive NDR2 null mutant mice, we demonstrate that Ndr2 deficiency leads to a reduction of T788/789 phosphorylated β1 integrin expression at synaptic sites both in the hippocampal area CA1 and in primary hippocampal neurons in vitro. This reduction is associated with decreased synaptic density in both conditions and accompanied by reduced long‐term potentiation in the synapses between Schaffer collaterals/commissural fibers and CA1 pyramidal cells, which could be restored by activation of integrins with an arginine‐glycine‐aspartate‐containing peptide, as well as with mild spatial memory deficits. Together, our results suggest that NDR2 is involved in integrin‐dependent synapse formation and plasticity in the mouse hippocampus.

Ndr2 participates in the T788/789 phosphorylation of the integrin β1 integrin subunit. Ndr2 deficiency reduces synaptic density, diminishes CA1 LTP, and impairs spatial memory. Activation of integrins restores the plasticity impairment of Ndr2 deficient mice. Ndr2 is involved in integrin‐dependent synapse formation and plasticity in the hippocampus CA1.

## Linked entities

- **Genes:** STK38L (serine/threonine kinase 38 like) [NCBI Gene 23012], MS4A1 (membrane spanning 4-domains A1) [NCBI Gene 931]
- **Proteins:** STK38L (serine/threonine kinase 38 like)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Map3k10 (mitogen-activated protein kinase kinase kinase 10) [NCBI Gene 269881] {aka MST, Mlk2}, Stk38l (serine/threonine kinase 38 like) [NCBI Gene 232533] {aka 4930473A22Rik, Ndr2, Ndr54}
- **Diseases:** memory deficits (MESH:D008569)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12120816/full.md

## References

79 references — full list in the complete paper: https://tomesphere.com/paper/PMC12120816/full.md

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Source: https://tomesphere.com/paper/PMC12120816