Literature DB >> 6197439

A new methodological approach for studying axonal transport: cytofluorometric scanning of nerves.

P A Larsson, M Goldstein, A Dahlström.   

Abstract

A new technique for studying axonal transport has been developed. The technique, which is based on histofluorescence techniques, enables the measurement of several different accumulated substances and parameters within a single nerve in relation to a nerve crush or local cooling. Any substance that can be made to fluoresce can be measured. The tissue is treated according to the formaldehyde-induced fluorescence method of Hillarp and Falck for visualization of monoamines, or according to the indirect immunofluorescence method. For immunofluorescence the nerve is cryostat-sectioned and various sections can be incubated with primary antisera against different antigens. After incubation and mounting the sections are placed in a cytofluorimeter (Leitz MPV II). They are passed under a measuring slit at a steady speed by a motor driven cross-table. The fluorescence intensity passing through the measuring slit is continuously registered by a recording unit with an integrator. This recorder produces a graphical nerve accumulation profile, and the area under the profile, relating to the fluorescence, is expressed in arbitrary units. This article presents data on the accumulation of noradrenaline, dopamine beta-hydroxylase, and tyrosine hydroxylase in crush-operated rat sciatic nerve. The time-course accumulations for noradrenaline (visualized by the Falck and Hillarp method) and dopamine beta-hydroxylase (visualized by immunofluorescence) demonstrated a striking similarity, which is to be expected since the two substances are stored in the same organelle. Tyrosine hydroxylase (visualized by immunofluorescence) showed a slower accumulation with time, but faster than would be expected had the enzyme been 100% soluble. Colchicine but not lumi-colchicine blocked the transport of noradrenaline organelles. With the new scanning technique we have the potential to study accumulation profiles of several different substances within a single nerve. Morphometric data, morphological observations, and photograph documentation of the same nerve section are also available.

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Year:  1984        PMID: 6197439     DOI: 10.1177/32.1.6197439

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  4 in total

Review 1.  Organelles in fast axonal transport. What molecules do they carry in anterograde vs retrograde directions, as observed in mammalian systems?

Authors:  A B Dahlström; A J Czernik; J Y Li
Journal:  Mol Neurobiol       Date:  1992 Summer-Fall       Impact factor: 5.590

Review 2.  Fast and slow axonal transport-different methodological approaches give complementary information: contributions of the stop-flow/crush approach.

Authors:  A B Dahlström; J Y Li
Journal:  Neurochem Res       Date:  1994-11       Impact factor: 3.996

3.  Quantitative immunofluorescence of tyrosine hydroxylase in the adrenal medulla of spontaneously hypertensive rats.

Authors:  I Nagatsu; M Ito; Y Kawakami; N Karasawa; H Takahashi; K Fujita; T Nagatsu
Journal:  Experientia       Date:  1985-08-15

4.  The synthesis of NPY and DBH is independently regulated in adrenergic nerves after reserpine.

Authors:  A Dahlström; S Bööj; M Goldstein; P A Larsson
Journal:  Neurochem Res       Date:  1987-03       Impact factor: 3.996

  4 in total

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