Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1966 Nov 1;31(2):215–242. doi: 10.1083/jcb.31.2.215

ACETYLCHOLINESTERASE IN FROG SYMPATHETIC AND DORSAL ROOT GANGLIA

A Study by Electron Microscope Cytochemistry and Microgasometric Analysis with the Magnetic Diver

Miro Brzin 1, Virginia M Tennyson 1, Philip E Duffy 1
PMCID: PMC2107049  PMID: 19866698

Abstract

The localization and chemical determination of acetylcholin esterase in the frog sympathetic and dorsal root ganglia were studied by a combination of the methods of electron microscopy, histochemistry, and microgasometric analysis with the magnetic diver. The Koelle-Friedenwald copper thiocholine histochemical method was modified by eliminating the sulfide conversion and by treatment of the tissue with potassium permanganate. In fixed tissue, enzymatic activity was demonstrated on the inner surface of the endoplasmic reticulum, nuclear envelope, subsurface cisternae, and agranular reticulum of the perikaryon and axon. In briefly fixed tissue, end product appeared also at the axon-sheath and the sheath-sheath interface. Activity at the synaptic junction was most readily obtained in unfixed tissue. Isolated neurons recovered from the diver following chemical analysis were studied with the electron microscope. Cells having a high enzyme activity showed a badly ruptured or absent neural plasmalemma and sheath. In this case the measured activity was apparently due to the enzyme present in the endoplasmic reticulum. Neurons having low activity exhibited an intact plasmalemma and sheath. This may reflect the effectiveness of the neural plasmalemma and sheath as a penetration barrier. The effects of fixation on enzyme activity are discussed. Electron microscopic examination of cells following microgasometric analysis is shown to be essential for the interpretation of the biochemical data.

Full Text

The Full Text of this article is available as a PDF (3.1 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ALDRIDGE W. N., JOHNSON M. K. Cholinesterase, succinic dehydrogenase, nucleic acids, esterase and glutathione reductase in sub-cellular fractions from rat brain. Biochem J. 1959 Oct;73:270–276. doi: 10.1042/bj0730270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BARRNETT R. J. The fine structural localization of acetylcholinesterase at the myoneural junction. J Cell Biol. 1962 Feb;12:247–262. doi: 10.1083/jcb.12.2.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BRZIN M., MAJCEN-TKACEV Z. CHOLINESTERASE IN DENERVATED END PLATES AND MUSCLE FIBRES. J Cell Biol. 1963 Nov;19:349–358. doi: 10.1083/jcb.19.2.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BRZIN M., ZEUTHEN E. NOTES ON THE POSSIBLE USE OF THE MAGNETIC DIVER FOR RESPIRATION MEASUREMENTS (ERROR 0.000001 MICRON 1/HOUR). C R Trav Lab Carlsberg. 1964;34:427–431. [PubMed] [Google Scholar]
  5. CLOUET D. H., WAELSCH H. Amino acid and protein metabolism of the brain--VIII. The recovery of cholinesterase in the nervous system of the frog after inhibition. J Neurochem. 1961 Dec;8:201–215. doi: 10.1111/j.1471-4159.1961.tb13544.x. [DOI] [PubMed] [Google Scholar]
  6. DE LORENZO A. J. Electron microscopy of the cerebral cortex. I. The ultrastructure and histochemistry of synaptic junctions. Bull Johns Hopkins Hosp. 1961 Apr;108:258–279. [PubMed] [Google Scholar]
  7. FUKUDA T., KOELLE G. B. The cytological localization of intracellular neuronal acetylcholinesterase. J Biophys Biochem Cytol. 1959 May 25;5(3):433–440. doi: 10.1083/jcb.5.3.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. FULTON M. P., MOGEY G. A. Some selective inhibitors of true cholinesterase. Br J Pharmacol Chemother. 1954 Jun;9(2):138–144. doi: 10.1111/j.1476-5381.1954.tb00832.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GIACOBINI E. Quantitative determination of cholinesterase in individual sympathetic cells. J Neurochem. 1957;1(3):234–244. doi: 10.1111/j.1471-4159.1957.tb12077.x. [DOI] [PubMed] [Google Scholar]
  10. GRAMPP W., EDSTROEM J. E. THE EFFECT OF NERVOUS ACTIVITY ON RIBONUCLEIC ACID OF THE CRUSTACEAN RECEPTOR NEURON. J Neurochem. 1963 Oct;10:725–731. doi: 10.1111/j.1471-4159.1963.tb08928.x. [DOI] [PubMed] [Google Scholar]
  11. KARNOVSKY M. J. THE LOCALIZATION OF CHOLINESTERASE ACTIVITY IN RAT CARDIAC MUSCLE BY ELECTRON MICROSCOPY. J Cell Biol. 1964 Nov;23:217–232. doi: 10.1083/jcb.23.2.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. KOELLE G. B., FOROGLOU-KERAMEOS C. ELECTRON MICROSCOPIC LOCALIZATION OF CHOLINESTERASES IN A SYMPATHETIC GANGLION BY A GOLD-THIOLACETIC ACID METHOD. Life Sci. 1965 Feb;4:417–424. doi: 10.1016/0024-3205(65)90161-x. [DOI] [PubMed] [Google Scholar]
  13. KOELLE G. B., FRIEDENWALD J. A. A histochemical method for localizing cholinesterase activity. Proc Soc Exp Biol Med. 1949 Apr;70(4):617–622. doi: 10.3181/00379727-70-17013. [DOI] [PubMed] [Google Scholar]
  14. KOELLE G. B. The histochemical identification of acetylcholinesterase in cholinergic, adrenergic and sensory neurons. J Pharmacol Exp Ther. 1955 Jun;114(2):167–184. [PubMed] [Google Scholar]
  15. KOENIG E., KOELLE G. B. Mode of regeneration of acetylcholinesterase in cholinergic neurons following irreversible inactivation. J Neurochem. 1961 Dec;8:169–188. doi: 10.1111/j.1471-4159.1961.tb13542.x. [DOI] [PubMed] [Google Scholar]
  16. KOENIG E. SYNTHETIC MECHANISMS IN THE AXON. II. RNA IN MYELIN-FREE AXONS OF THE CAT. J Neurochem. 1965 May;12:357–361. doi: 10.1111/j.1471-4159.1965.tb04236.x. [DOI] [PubMed] [Google Scholar]
  17. LAVERTY R., MICHAELSON I. A., SHARMAN D. F., WHITTAKER V. P. THE SUBCELLULAR LOCALIZATION OF DOPAMINE AND ACETYLCHOLINE IN THE DOG CAUDATE NUCLEUS. Br J Pharmacol Chemother. 1963 Dec;21:482–490. doi: 10.1111/j.1476-5381.1963.tb02016.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. LEHRER G. M., ORNSTEIN L. A diazo coupling method for the electron microscopic localization of cholinesterase. J Biophys Biochem Cytol. 1959 Dec;6:399–406. doi: 10.1083/jcb.6.3.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. LUFT J. H. Permanganate; a new fixative for electron microscopy. J Biophys Biochem Cytol. 1956 Nov 25;2(6):799–802. doi: 10.1083/jcb.2.6.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. METUZALS J. Ultrastructure of myelinated nerve fibers in the central nervous system of the frog. J Ultrastruct Res. 1963 Feb;8:30–47. doi: 10.1016/s0022-5320(63)80019-2. [DOI] [PubMed] [Google Scholar]
  22. MILEDI R. ELECTRON-MICROSCOPICAL LOCALIZATION OF PRODUCTS FROM HISTOCHEMICAL REACTIONS USED TO DETECT CHOLINESTERASE IN MUSCLE. Nature. 1964 Oct 17;204:293–295. doi: 10.1038/204293b0. [DOI] [PubMed] [Google Scholar]
  23. NACHMANSOHN D. CHEMICAL CONTROL OF BIOELECTRIC CURRENTS IN MEMBRANES OF CONDUCTING CELLS. J Mt Sinai Hosp N Y. 1964 Nov-Dec;31:549–583. [PubMed] [Google Scholar]
  24. PALADE G. E. A study of fixation for electron microscopy. J Exp Med. 1952 Mar;95(3):285–298. doi: 10.1084/jem.95.3.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. PICK J., GERDIN C., DELEMOS C. On the ultrastructure of spinal nerve roots in the frog (Rana pipiens). Anat Rec. 1963 May;146:61–84. doi: 10.1002/ar.1091460108. [DOI] [PubMed] [Google Scholar]
  26. PICK J. The submicroscopic organization of the sympathetic ganglion in the frog (Rana pipiens). J Comp Neurol. 1963 Jun;120:409–462. doi: 10.1002/cne.901200304. [DOI] [PubMed] [Google Scholar]
  27. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. ROBERTSON J. D., BODENHEIMER T. S., STAGE D. E. THE ULTRASTRUCTURE OF MAUTHNER CELL SYNAPSES AND NODES IN GOLDFISH BRAINS. J Cell Biol. 1963 Oct;19:159–199. doi: 10.1083/jcb.19.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. ROOTS B. I., JOHNSTON P. V. NEURONS OF OX BRAIN NUCLEI: THEIR ISOLATION AND APPEARANCE BY LIGHT AND ELECTRON MICROSCOPY. J Ultrastruct Res. 1964 Apr;10:350–361. doi: 10.1016/s0022-5320(64)80014-9. [DOI] [PubMed] [Google Scholar]
  30. ROSENBLUTH J. Contrast between osmium-fixed and permanganate-fixed toad spinal ganglia. J Cell Biol. 1963 Jan;16:143–157. doi: 10.1083/jcb.16.1.143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Roots B. I., Johnston P. V. Isolated rabbit neurones: electron microscopical observations. Nature. 1965 Jul 17;207(994):315–316. doi: 10.1038/207315a0. [DOI] [PubMed] [Google Scholar]
  32. SABATINI D. D., BENSCH K., BARRNETT R. J. Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation. J Cell Biol. 1963 Apr;17:19–58. doi: 10.1083/jcb.17.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. SHEN S. C., GREENFIELD P., BOELL E. J. The distribution of cholinesterase in the frog brain. J Comp Neurol. 1955 Jun;102(3):717–743. doi: 10.1002/cne.901020307. [DOI] [PubMed] [Google Scholar]
  34. Schlaepfer W. W., Torack R. M. The ultrastructural localization of cholinesterase activity in the sciatic nerve of the rat. J Histochem Cytochem. 1966 May;14(5):369–378. doi: 10.1177/14.5.369. [DOI] [PubMed] [Google Scholar]
  35. Smith D. S., Treherne J. E. The electron microscopic localization of cholinesterase activity in the central nervous system of an insect, Periplaneta americana 1. J Cell Biol. 1965 Aug;26(2):445–465. doi: 10.1083/jcb.26.2.445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. TAXI J. Action du formol sur l'activité de diverses préparations de cholinestérases. J Physiol (Paris) 1952;44(3):595–597. [PubMed] [Google Scholar]
  37. TOSCHI G. A biochemical study of brain microsomes. Exp Cell Res. 1959 Feb;16(2):232–255. doi: 10.1016/0014-4827(59)90252-6. [DOI] [PubMed] [Google Scholar]
  38. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. WATSON M. L. The nuclear envelope; its structure and relation to cytoplasmic membranes. J Biophys Biochem Cytol. 1955 May 25;1(3):257–270. doi: 10.1083/jcb.1.3.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. YAMAMOTO T. Some observations on the fine structure of the sympathetic ganglion of bullfrog. J Cell Biol. 1963 Jan;16:159–170. doi: 10.1083/jcb.16.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. ZAJICEK J., SYLVEN B., DATTA N. Attempts to demonstrate acetylcholinesterase activity in blood and bone-marrow cells by a modified thiocholine technique. J Histochem Cytochem. 1954 Mar;2(2):115–121. doi: 10.1177/2.2.115. [DOI] [PubMed] [Google Scholar]
  42. ZAJICEK J., ZEUTHEN E. Quantitative determination by a special "ampulla-diver" of cholinesterase activity in individual cells, with notes on other uses of the method. Gen Cytochem Methods. 1961;2:131–152. doi: 10.1016/b978-0-12-395584-5.50008-1. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES