Fluorescence microscopy of stimulated Zn(II) release from organotypic cultures of mammalian hippocampus using a carbonic anhydrase-based biosensor system

J Neurosci Methods. 2000 Mar 1;96(1):35-45. doi: 10.1016/s0165-0270(99)00183-1.

Abstract

We demonstrate here that electrical stimulation of organotypic cultures of rat hippocampus results in the prompt release of significant amounts of Zn(II) by a fluorescence microscopic method. The fluorescence imaging of free Zn(II) is achieved using a highly selective biosensing indicator system consisting of human apo-carbonic anhydrase II (apoCAII) and a fluorescent aryl sulfonamide inhibitor of the enzyme, ABD-N. The apoenzyme and ABD-N in the absence of Zn(II) exhibit weak, reddish fluorescence typical of the ABD-N alone; when Zn(II) is added it binds to the apoenzyme (K(D) = 4 pM), which strongly promotes binding of ABD-N to the holoenzyme (K(D) = 0.9 microM). Binding of ABD-N to the holoenzyme results in a 9-fold increase in apparent quantum yield, significant blue shifts in excitation and emission, an increase in average fluorescence lifetime, a 4-fold increase in the ratio of intensities at 560 and 680 nm, and a large increase in anisotropy. Prior to stimulation, cultures immersed in phosphate-buffered saline with glucose and apoCAII with ABD-N emitted negligible fluorescence, but within 20 s after electrical stimulation a diffuse cloud of greenish fluorescence emerged and subsequently covered most of the culture, indicating release of zinc into the extracellular medium.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Anisotropy
  • Biosensing Techniques / methods*
  • Carbonic Anhydrases / pharmacology*
  • Electric Stimulation
  • Hippocampus / metabolism*
  • Humans
  • Mammals
  • Microscopy, Fluorescence / methods*
  • Organ Culture Techniques
  • Oxadiazoles / chemical synthesis
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Sulfonamides / chemical synthesis
  • Zinc / metabolism*

Substances

  • 4-(aminosulfonyl)-7-(ethanolamino)-2,1,3-benzoxadiazole
  • Oxadiazoles
  • Recombinant Proteins
  • Sulfonamides
  • Carbonic Anhydrases
  • Zinc