Ectopic expression of metallothionein-III causes pancreatic acinar cell necrosis in transgenic mice

Toxicol Appl Pharmacol. 1998 Jan;148(1):148-57. doi: 10.1006/taap.1997.8321.


Mice express four distinct metallothioneins (MTs) that have similar metal-binding properties. MT-I and MT-II are expressed coordinately in most organs, whereas MT-III is expressed predominantly in a subset of neurons and MT-IV is expressed in certain stratified epithelia. The restricted expression of MT-III suggests that it may severe a specialized function. To test this hypothesis, transgenic mice were generated that express MT-III in the wider expression domain of MT-I. Similar transgenic lines expressing extra MT-I under the same regulation were generated as controls for the effect of over-expression of MT. Transgenic mice that express MT-III ectopically frequently die at 2-3 months of age. The pancreata of moribund mice were abnormally small and histological examination, at various ages, revealed a progressive degeneration of the acinar cells. At early stages multifocal acinar cell eosinophilia and swollen nuclei were seen and this pathology progressed to multifocal acinar cell necrosis and fibrosis. The terminal stages were characterized by a loss of the acinar compartment, leaving the islets embedded in a fibrotic remnant. Other organs of these mice were grossly and histologically normal. All organs examined from mice expressing excess MT-I were unremarkable even though expression of either MT-I or MT-III transgenes resulted in similar accumulations of zinc and copper in the pancreata. This study indicates that pancreatic acinar cells are unusually sensitive to chronic expression of MT-III. The mechanism by which MT-III disrupts pancreatic function is unclear, but the results provide further evidence that MT isoforms exhibit distinct properties and probably serve distinct biological functions.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Copper / metabolism
  • DNA Probes / chemistry
  • Diet
  • Female
  • Glucagon / metabolism
  • Growth Inhibitors / genetics
  • Growth Inhibitors / metabolism*
  • Insulin / metabolism
  • Male
  • Metallothionein / genetics
  • Metallothionein / metabolism
  • Mice
  • Mice, Transgenic / genetics
  • Necrosis
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Pancreas / metabolism
  • Pancreas / pathology*
  • RNA, Messenger / metabolism
  • Zinc / deficiency
  • Zinc / metabolism


  • DNA Probes
  • Growth Inhibitors
  • Insulin
  • Nerve Tissue Proteins
  • RNA, Messenger
  • growth inhibitory factor
  • Copper
  • Glucagon
  • Metallothionein
  • Zinc