Congenital Hyperinsulinism in Humans and Insulin Secretory Dysfunction in Mice Caused by Biallelic DNAJC3 Variants

Int J Mol Sci. 2024 Jan 20;25(2):1270. doi: 10.3390/ijms25021270.

Abstract

The BiP co-chaperone DNAJC3 protects cells during ER stress. In mice, the deficiency of DNAJC3 leads to beta-cell apoptosis and the gradual onset of hyperglycemia. In humans, biallelic DNAJC3 variants cause a multisystem disease, including early-onset diabetes mellitus. Recently, hyperinsulinemic hypoglycemia (HH) has been recognized as part of this syndrome. This report presents a case study of an individual with HH caused by DNAJC3 variants and provides an overview of the metabolic phenotype of individuals with HH and DNAJC3 variants. The study demonstrates that HH may be a primary symptom of DNAJC3 deficiency and can persist until adolescence. Additionally, glycemia and insulin release were analyzed in young DNACJ3 knockout (K.O.) mice, which are equivalent to human infants. In the youngest experimentally accessible age group of 4-week-old mice, the in vivo glycemic phenotype was already dominated by a reduced total insulin secretion capacity. However, on a cellular level, the degree of insulin release of DNAJC3 K.O. islets was higher during periods of increased synthetic activity (high-glucose stimulation). We propose that calcium leakage from the ER into the cytosol, due to disrupted DNAJC3-controlled gating of the Sec61 channel, is the most likely mechanism for HH. This is the first genetic mechanism explaining HH solely by the disruption of intracellular calcium homeostasis. Clinicians should screen for HH in DNAJC3 deficiency and consider DNAJC3 variants in the differential diagnosis of congenital hyperinsulinism.

Keywords: BiP/GRP78 co-chaperone; calcium leak; endoplasmic reticulum stress; hyperinsulinemic hypoglycemia; intracellular calcium homeostasis; monogenic diabetes.

MeSH terms

  • Adolescent
  • Animals
  • Calcium / metabolism
  • Congenital Hyperinsulinism* / genetics
  • HSP40 Heat-Shock Proteins* / genetics
  • HSP40 Heat-Shock Proteins* / metabolism
  • Humans
  • Insulin / metabolism
  • Insulin Secretion
  • Mice
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism

Substances

  • Calcium
  • DNAJC3 protein, human
  • HSP40 Heat-Shock Proteins
  • Insulin
  • Molecular Chaperones
  • Dnajc3 protein, mouse

Grants and funding

The work was funded by the Leonard-Thompson research grant from the AGPD (Arbeitsgemeinschaft für Pädiatrische Diabetologie e.V.).