# Heat shock protein DNAJA2 controls insulin signaling and glucose homeostasis by preventing spontaneous insulin receptor endocytosis

**Authors:** Yuanhua Qin, Wenjun Wu, Kequan Lin, Anthony J. Davis, Yaping Huang

PMC · DOI: 10.1038/s41467-025-64948-0 · 2025-11-13

## TL;DR

DNAJA2, a heat shock protein, helps regulate insulin signaling and glucose metabolism by preventing insulin receptor endocytosis, and its absence leads to metabolic disorders like diabetes.

## Contribution

This study reveals DNAJA2's novel role in preventing spontaneous insulin receptor endocytosis, linking it to glucose homeostasis and metabolic diseases.

## Key findings

- DNAJA2 binds to the insulin receptor and inhibits AP2-mediated endocytosis.
- Loss of DNAJA2 reduces insulin receptor localization and impairs insulin signaling.
- DNAJA2 deficiency leads to neonatal lethality and is associated with metabolic disorders like T2DM and obesity.

## Abstract

Dysregulation of heat shock protein DNAJA2 induces genomic instability and was consequently hypothesized to promote tumorigenesis. However, DNAJA2 knockout mice do not develop cancer but exhibit neonatal lethality and the underlying mechanism remains unknown. Here, we demonstrate that DNAJA2 maintains homeostatic glucose metabolism by regulating insulin signaling. Mechanistically, DNAJA2 binds to the insulin receptor (IR) and prevents adaptor protein 2 (AP2)-mediated spontaneous IR endocytosis by inhibiting the IR-AP2 interaction. Thus, DNAJA2 defects lead to reduced IR localization on the plasma membrane and suppression of the insulin-stimulated signaling cascade, thereby inhibiting glycogen synthesis and storage in the liver during embryogenesis, further resulting in neonatal lethality of DNAJA2-deficient mice. Analysis of public datasets reveals a strong association between DNAJA2 and metabolic phenotypes, including type 2 diabetes mellitus (T2DM) and obesity, in both humans and mice. In conclusion, our study elucidates the mechanism by which DNAJA2 regulates IR endocytosis, insulin signaling and glucose metabolism, shedding light on the pathogenesis of metabolic disorders.

Insulin signaling pathway is critical for glucose homeostasis maintenance. Here, the authors identify a role for DNAJA2 in regulating insulin signaling and glucose metabolism, loss of which causes insulin resistance and type 2 diabetes phenotypes.

## Linked entities

- **Genes:** DNAJA2 (DnaJ heat shock protein family (Hsp40) member A2) [NCBI Gene 10294], FABP4 (fatty acid binding protein 4) [NCBI Gene 2167], Insr (insulin receptor) [NCBI Gene 16337]
- **Proteins:** DNAJA2 (DnaJ heat shock protein family (Hsp40) member A2)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), obesity (MONDO:0011122)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Insr (insulin receptor) [NCBI Gene 16337] {aka 4932439J01Rik, CD220, D630014A15Rik, IR, IR-A, IR-B}, Tfap2a (transcription factor AP-2, alpha) [NCBI Gene 21418] {aka AP-2, AP2alpha, Ap-2 (a), Ap2, Ap2tf, Tcfap2a}, Dnaja2 (DnaJ heat shock protein family (Hsp40) member A2) [NCBI Gene 56445] {aka 1500017M13Rik, 2010206B19Rik, DNAJ, DNJ3, Dnaj3, HIRIP4}
- **Diseases:** T2DM (MESH:D003924), cancer (MESH:D009369), tumorigenesis (MESH:D063646), neonatal lethality (MESH:C537510), obesity (MESH:D009765), metabolic disorders (MESH:D008659)
- **Chemicals:** glycogen (MESH:D006003), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615670/full.md

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Source: https://tomesphere.com/paper/PMC12615670