Literature DB >> 1614832

A fast perfusion system for single cell physiology optimized for microscopes with water immersion objectives.

F Kirchhoff1, C Ohlemeyer, H Kettenmann.   

Abstract

A perfusion system was constructed which allows the fast application of different solutes underneath a water immersion objective. The perfusion system is mounted into the immersion objective by milling a slot into the frontal metal plate of the lens holder. It consists of a five-channel pipette fixed to the objective and solution reservoirs gated by computer controlled magnetic valves. Up to five different solutions can be applied to the specimen under study. The solution between objective and specimen is completely exchanged after 1-2 s as determined from fluorescence measurements. This arrangement is optimized for [Ca2+] measurements with a fluorescence measurement system in tissue slices, where upright microscopes are required. It offers the advantage of saving a micromanipulator for the perfusion pipette and facilitates a fast, reproducible and precise positioning of the perfusion system.

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Year:  1992        PMID: 1614832     DOI: 10.1007/bf00374635

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  10 in total

Review 1.  Fluorescent probes of cell signaling.

Authors:  R Y Tsien
Journal:  Annu Rev Neurosci       Date:  1989       Impact factor: 12.449

2.  Lucifer dyes--highly fluorescent dyes for biological tracing.

Authors:  W W Stewart
Journal:  Nature       Date:  1981-07-02       Impact factor: 49.962

3.  Monoclonal antibodies (O1 to O4) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system.

Authors:  I Sommer; M Schachner
Journal:  Dev Biol       Date:  1981-04-30       Impact factor: 3.582

4.  A new generation of Ca2+ indicators with greatly improved fluorescence properties.

Authors:  G Grynkiewicz; M Poenie; R Y Tsien
Journal:  J Biol Chem       Date:  1985-03-25       Impact factor: 5.157

5.  Activation of substance P receptors leads to membrane potential responses in cultured astrocytes.

Authors:  M Wienrich; H Kettenmann
Journal:  Glia       Date:  1989       Impact factor: 7.452

6.  Expression of Thy-1, H-2, and NS-4 cell surface antigens and tetanus toxin receptors in early postnatal and adult mouse cerebellum.

Authors:  J Schnitzer; M Schachner
Journal:  J Neuroimmunol       Date:  1981-12       Impact factor: 3.478

7.  Differentiation-regulated loss of the polysialylated embryonic form and expression of the different polypeptides of the neural cell adhesion molecule by cultured oligodendrocytes and myelin.

Authors:  J Trotter; D Bitter-Suermann; M Schachner
Journal:  J Neurosci Res       Date:  1989-04       Impact factor: 4.164

8.  Aspartate, glutamate and gamma-aminobutyric acid depolarize cultured astrocytes.

Authors:  H Kettenmann; K H Backus; M Schachner
Journal:  Neurosci Lett       Date:  1984-11-23       Impact factor: 3.046

9.  Site and mechanism of activation of proton-induced sodium current in chick dorsal root ganglion neurones.

Authors:  N W Davies; H D Lux; M Morad
Journal:  J Physiol       Date:  1988-06       Impact factor: 5.182

10.  Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue.

Authors:  K D McCarthy; J de Vellis
Journal:  J Cell Biol       Date:  1980-06       Impact factor: 10.539

  10 in total
  2 in total

1.  An automatic monitoring system for epithelial cell height.

Authors:  W Van Driessche; P De Smet; G Raskin
Journal:  Pflugers Arch       Date:  1993-10       Impact factor: 3.657

2.  Kainate activates Ca(2+)-permeable glutamate receptors and blocks voltage-gated K+ currents in glial cells of mouse hippocampal slices.

Authors:  R Jabs; F Kirchhoff; H Kettenmann; C Steinhäuser
Journal:  Pflugers Arch       Date:  1994-02       Impact factor: 3.657

  2 in total

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