# Hippocalcin Regulates NMDA Receptor Function and Neuronal Activity Through Elavl3 in Mouse Hippocampal Neural Precursor Cells

**Authors:** Min-Jeong Kang, Sung Jun Jung, Hyeon Son, Joong-Soo Han, Shin-Young Park

PMC · DOI: 10.3390/ijms27052439 · 2026-03-06

## TL;DR

This study shows that Hippocalcin (HPCA) regulates NMDA receptors and neuronal activity in mouse hippocampal cells through Elavl3, impacting brain function and behavior.

## Contribution

The study identifies Elavl3 as a novel downstream mediator of HPCA in regulating NMDA receptor function and neuronal development.

## Key findings

- HPCA knockdown reduces NMDA receptor-related gene expression and calcium signaling in mouse hippocampal neural precursor cells.
- Elavl3 suppression mimics HPCA deficiency, impairing NMDA receptor activity and neuronal differentiation.
- HPCA knockdown in vivo alters locomotor activity, memory, and affective behaviors in mice.

## Abstract

Hippocalcin (HPCA), a neuron-enriched calcium-binding protein, plays a critical role in brain function, but its role in neural precursor cells remains unclear. N-methyl-D-aspartate (NMDA) receptors are calcium-permeable glutamate receptors essential for neurodevelopment and synaptic plasticity, and their function has been implicated in neurological conditions. In this study, we investigated the role of HPCA in regulating NMDA receptor expression and function in mouse hippocampal neural precursor cells (mHNPCs). HPCA knockdown significantly reduced the expression of NMDA receptor-related genes, including Grin2C, Shank1, Serpine2, and selectively attenuated NMDA-induced calcium signaling. Transcriptomic analysis identified ELAV-like RNA-binding protein 3 (Elavl3), a neuron-enriched factor associated with neuronal activity, as a downstream candidate affected by HPCA knockdown. Consistently, Elavl3 suppression phenocopied HPCA deficiency, resulting in impaired NMDA receptor activity and reduced neuronal differentiation. Furthermore, hippocampal HPCA knockdown in vivo led to alterations in locomotor activity, contextual memory, and affective behaviors. Taken together, these findings demonstrate that HPCA supports NMDA receptor function and neuronal development, in part through Elavl3-associated pathways, and highlight HPCA as an important regulator of hippocampal function.

## Linked entities

- **Genes:** HPCA (hippocalcin) [NCBI Gene 3208], GRIN2C (glutamate ionotropic receptor NMDA type subunit 2C) [NCBI Gene 2905], SHANK1 (SH3 and multiple ankyrin repeat domains 1) [NCBI Gene 50944], SERPINE2 (serpin family E member 2) [NCBI Gene 5270], ELAVL3 (ELAV like RNA binding protein 3) [NCBI Gene 1995]
- **Proteins:** Nca (neurocalcin homolog)
- **Chemicals:** N-methyl-D-aspartate (PubChem CID 22880)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Serpine2 (serine (or cysteine) peptidase inhibitor, clade E, member 2) [NCBI Gene 20720] {aka B230326M24Rik, PAI-1, PI-7, PI7, PN-1, Spi4}, Grin2c (glutamate receptor, ionotropic, NMDA2C (epsilon 3)) [NCBI Gene 14813] {aka GluN2C, NMDAR2C, NR2C}, Hpca (hippocalcin) [NCBI Gene 15444], Shank1 (SH3 and multiple ankyrin repeat domains 1) [NCBI Gene 243961], Elavl3 (ELAV like RNA binding protein 3) [NCBI Gene 15571] {aka 2600009P04Rik, Huc, PLE21, mHuC}
- **Diseases:** HPCA deficiency (MESH:D007153), neurological conditions (MESH:D019636)
- **Chemicals:** calcium (MESH:D002118)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985563/full.md

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Source: https://tomesphere.com/paper/PMC12985563