Literature DB >> 6487898

Development of markers for cholinergic neurones in re-aggregate cultures of foetal rat whole brain in serum-containing and serum-free media: effects of triiodothyronine (T3).

C K Atterwill, A Kingsbury, J Nicholls, A Prince.   

Abstract

Development has been studied in re-aggregate cultures derived from the 16 day foetal rat brain and the effects of triiodothyronine (T3) investigated. Cultures were maintained in either a medium containing 10% serum (S+), or in serum-free culture medium (S-) or in serum-free medium containing 30nM T3. The muscarinic cholinoceptor, measured by specific binding of [3H]-quinuclidinyl benzitate ([3H]-QNB) at 9 and 14 days in vitro, was at a lower level in the serum-free cultured cells compared with those in serum-containing culture medium (S+). In cultures in the latter medium, receptor concentration at day 14 was of a similar magnitude to that in rat brain at an equivalent postnatal age. Binding increased with development from 9 to 14 days in vitro in the S+ medium but not in the S- medium. T3 treatment caused an 85% increase in [3H]-QNB binding compared with the cultures in S- medium at day 14 to a level equivalent to that found in the cells grown in S+ medium. This increase was reflected in the Bmax but not in the KD (approx. 0.1nM). Choline acetyltransferase (ChAT) activity developed more slowly in the S- medium than in the S+ medium where the specific activity approximated values obtained in vivo. T3 treatment of cultures grow in S- medium significantly enhanced the developmental rate of increase of ChAT activity. The characteristics of [3H]-choline uptake and metabolism in the cultures was examined. Uptake was strictly Na+-independent but was energy-dependent, and inhibited by 2, 4'-dinitrophenol (2, 4'-DNP) and cooling (0-4 degrees C). Neither iodoacetate nor ouabain had any effect on the amount of uptake. Hemicholinium (HC3) was a potent inhibitor of uptake (70% inhibition at 10 microM HC3). Metabolism studies showed virtually no conversion to [3H]-acetylcholine ([3H]-ACH) in reaggregates grown in either the S+, S- or T3 containing media. However, a small amount of [3H]-choline was incorporated into phosphorylcholine. T3 treatment had no effect on this metabolic profile. The kinetics of [3H]-choline uptake by the re-aggregates was also studied in the re-aggregate cultures (after 12 and 22 days in vitro) using [3H]-choline at 0.05-100 microM. Both Eadie-Hofstee transformation and least-squares analysis of the data showed that the uptake comprised only a single low-affinity component with an apparent Kt = approx. 50 microM. Unlike ChAT and [3H]-QNB binding, there appeared to be no difference between the uptake in the different culture conditions. 6 It is concluded that the differentiation of cholinergic neurones and muscarinic receptors in serum-free cultured re-aggregates from foetal rat brain is enhanced by thyroid hormone treatment. The development of [3H]-choline uptake does not seem to be associated with cholinergic cells under these culture conditions, and is unaffected by thyroid hormone treatment.

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Year:  1984        PMID: 6487898      PMCID: PMC1987186          DOI: 10.1111/j.1476-5381.1984.tb10123.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  37 in total

1.  Utilization of sodium-dependent high affinity choline uptake in vitro as a measure of the activity of cholinergic neurons in vivo.

Authors:  S Atweh; J R Simon; M J Kuhar
Journal:  Life Sci       Date:  1975-11-15       Impact factor: 5.037

2.  Biochemical differentiation of mechanically dissociated mammalian brain in aggregating cell culture.

Authors:  P Honegger; E Richelson
Journal:  Brain Res       Date:  1976-06-11       Impact factor: 3.252

3.  A rapid radiochemical method for the determination of choline acetyltransferase.

Authors:  F Fonnum
Journal:  J Neurochem       Date:  1975-02       Impact factor: 5.372

4.  Increased uptake of choline by neural cell cultures chronically exposed to ethanol.

Authors:  R Massarelli; P J Syapin; E P Noble
Journal:  Life Sci       Date:  1976-02-15       Impact factor: 5.037

5.  High affinity choline uptake: an early index of cholinergic innervation in rat brain.

Authors:  M Sorimachi; K Kataoka
Journal:  Brain Res       Date:  1975-08-29       Impact factor: 3.252

6.  Selective localization of a high affinity choline uptake system and its role in ACh formation in cholinergic nerve terminals.

Authors:  J B Suszkiw; G Pilar
Journal:  J Neurochem       Date:  1976-06       Impact factor: 5.372

7.  Cholinesterase activity and choline uptake in intact nerve cell cultures.

Authors:  R Massarelli; V Stefanovic; P Mandel
Journal:  Brain Res       Date:  1976-08-06       Impact factor: 3.252

8.  Choline uptake in glial cell cultures.

Authors:  R Massarelli; J Ciesielski-Treska; A Ebel; P Mandel
Journal:  Brain Res       Date:  1974-12-06       Impact factor: 3.252

9.  Alterations of brain acetylcholine metabolism during neonatal hyperthyroidism.

Authors:  R B Rastogi; P D Hrdina; T Dubas; R L Singhal
Journal:  Brain Res       Date:  1977-03-04       Impact factor: 3.252

10.  The metabolism of labelled choline in neuronal and glial cells of the rabbit in vivo.

Authors:  E Francescangeli; G Goracci; G L Piccinin; R Mozzi; H Woelk; G Porcellati
Journal:  J Neurochem       Date:  1977-01       Impact factor: 5.372

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  4 in total

1.  Thyroid hormone regulates Na+ currents in cultured hippocampal neurons from postnatal rats.

Authors:  O Potthoff; I D Dietzel
Journal:  Proc Biol Sci       Date:  1997-03-22       Impact factor: 5.349

2.  Effects of methyl isocyanate on rat brain cells in culture.

Authors:  D Anderson; S Goyle; B J Phillips; A Tee; L Beech; W H Butler
Journal:  Br J Ind Med       Date:  1990-09

3.  Stimulation of acetylcholinesterase activity by triiodothyronine in the brain of Singi fish, Heteropneustes fossilis (Bloch).

Authors:  S De; A K Dasmahapatra; A K Medda
Journal:  Fish Physiol Biochem       Date:  1993-03       Impact factor: 2.794

4.  Neurotrophic factor for central cholinergic neurones is present in both normal and Alzheimer brain tissue.

Authors:  C K Atterwill; D M Bowen
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

  4 in total

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