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. 1970 Jun 1;45(3):565–575. doi: 10.1083/jcb.45.3.565

LOW RESISTANCE CONNECTIONS BETWEEN CELLS IN THE DEVELOPING ANTHER OF THE LILY

Nicholas C Spitzer 1
PMCID: PMC2107936  PMID: 4918215

Abstract

Low resistance junctions were demonstrated between cells in anthers from young buds of Lilium longiflorum Croft by standard electrophysiological techniques. Electrodes containing a dye were used to stain impaled cells for later histological identification. Electrical coupling is widespread; germinal cells are coupled to one another; coupling is also observed between somatic elements, and germinal and somatic cells are similarly interconnected. Cytoplasmic bridges are implicated in the first case; plasmodesmata are probably responsible for the interactions in the other two. Although the physiological role of the low resistance junctions shown here and present in embryonic animal tissues is unknown, the possible function of this form of intercellular communication in the development of the anther is discussed.

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Selected References

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  1. BENNETT M. V., ALJURE E., NAKAJIMA Y., PAPPAS G. D. Electrotonic junctions between teleost spinal neurons: electrophysiology and ultrastructure. Science. 1963 Jul 19;141(3577):262–264. doi: 10.1126/science.141.3577.262. [DOI] [PubMed] [Google Scholar]
  2. Bennett M. V., Nakajima Y., Pappas G. D. Physiology and ultrastructure of electrotonic junctions. I. Supramedullary neurons. J Neurophysiol. 1967 Mar;30(2):161–179. doi: 10.1152/jn.1967.30.2.161. [DOI] [PubMed] [Google Scholar]
  3. Echlin P., Godwin H. The ultrastructure and ontogeny of pollen in Helleborus foetidus L. I. The development of the tapetum and Ubisch bodies. J Cell Sci. 1968 Jun;3(2):161–174. doi: 10.1242/jcs.3.2.161. [DOI] [PubMed] [Google Scholar]
  4. Echlin P., Godwin H. The ultrastructure and ontogeny of pollen in Helleborus foetidus L. II. Pollen grain development through the callose special wall stage. J Cell Sci. 1968 Jun;3(2):175–186. doi: 10.1242/jcs.3.2.175. [DOI] [PubMed] [Google Scholar]
  5. FURSHPAN E. J., POTTER D. D. Transmission at the giant motor synapses of the crayfish. J Physiol. 1959 Mar 3;145(2):289–325. doi: 10.1113/jphysiol.1959.sp006143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gillespie B., Thimann K. V. Transport & Distribution of Auxin during Tropistic Response. I. The Lateral Migration of Auxin in Geotropism. Plant Physiol. 1963 Mar;38(2):214–225. doi: 10.1104/pp.38.2.214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ito M., Stern H. Studies of meiosis in vitro. I. In vitro culture of meiotic cells. Dev Biol. 1967 Jul;16(1):36–53. doi: 10.1016/0012-1606(67)90016-4. [DOI] [PubMed] [Google Scholar]
  8. Ito S., Hori N. Electrical characteristics of Triturus egg cells during cleavage. J Gen Physiol. 1966 May;49(5):1019–1027. doi: 10.1085/jgp.49.5.1019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. KUFFLER S. W., POTTER D. D. GLIA IN THE LEECH CENTRAL NERVOUS SYSTEM: PHYSIOLOGICAL PROPERTIES AND NEURON-GLIA RELATIONSHIP. J Neurophysiol. 1964 Mar;27:290–320. doi: 10.1152/jn.1964.27.2.290. [DOI] [PubMed] [Google Scholar]
  10. LOEWENSTEIN W. R., KANNO Y. STUDIES ON AN EPITHELIAL (GLAND) CELL JUNCTION. I. MODIFICATIONS OF SURFACE MEMBRANE PERMEABILITY. J Cell Biol. 1964 Sep;22:565–586. doi: 10.1083/jcb.22.3.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Loewenstein W. R., Socolar S. J., Higashino S., Kanno Y., Davidson N. Intercellular Communication: Renal, Urinary Bladder, Sensory, and Salivary Gland Cells. Science. 1965 Jul 16;149(3681):295–298. doi: 10.1126/science.149.3681.295. [DOI] [PubMed] [Google Scholar]
  12. PORTER K. R., MACHADO R. D. Studies on the endoplasmic reticulum. IV. Its form and distribution during mitosis in cells of onion root tip. J Biophys Biochem Cytol. 1960 Feb;7:167–180. doi: 10.1083/jcb.7.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pappas G. D., Bennett M. V. Specialized junctions involved in electrical transmission between neurons. Ann N Y Acad Sci. 1966 Jul 14;137(2):495–508. doi: 10.1111/j.1749-6632.1966.tb50177.x. [DOI] [PubMed] [Google Scholar]
  14. Penn R. D. Ionic communication between liver cells. J Cell Biol. 1966 Apr;29(1):171–174. doi: 10.1083/jcb.29.1.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Potter D. D., Furshpan E. J., Lennox E. S. Connections between cells of the developing squid as revealed by electrophysiological methods. Proc Natl Acad Sci U S A. 1966 Feb;55(2):328–336. doi: 10.1073/pnas.55.2.328. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Shah B. H., Wedding R. T. Sodium ion influences on phosphorylations associated with oxidation of succinate by turnip root mitochondria. Science. 1968 Apr 19;160(3825):304–306. doi: 10.1126/science.160.3825.304. [DOI] [PubMed] [Google Scholar]
  17. Stern H., Hotta Y. Biochemical studies of male gametogenesis in liliaceous plants. Curr Top Dev Biol. 1968;3:37–63. doi: 10.1016/s0070-2153(08)60350-6. [DOI] [PubMed] [Google Scholar]
  18. TAYLOR J. H., McMASTER R. D. Autoradiographic and microphotometric studies of desoxyribose nucleic acid during microgametogenesis in Lilium longiflorum. Chromosoma. 1954;6(6-7):489–521. doi: 10.1007/BF01259951. [DOI] [PubMed] [Google Scholar]

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