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. 1968 Mar 1;36(3):527–549. doi: 10.1083/jcb.36.3.527

MORPHOLOGICAL AND FUNCTIONAL ASPECTS OF AN INSECT EPIDERMAL GLAND

A M Stuart 1, P Satir 1
PMCID: PMC2107364  PMID: 5645546

Abstract

The sternal gland of primitive termites of the genus Zootermopsis (Z. nevadensis or Z. angusticollus) (Hagen) seems more organized than that of higher termites, in being comprised of three cell layers. It is also studded with about 200 campaniform sensilla. Below the meshwork cuticle of the gland lies a layer of columnar epithelial cells whose apical surfaces form a brush border, and whose basal surfaces are sculptured into a basketwork into which the second layer fits. Below the brush border are small microtubule-associated pits and coated vesicles. No channels can be seen either within or, except for the sensilla, between the cells. The second cell layer probably secretes the trail-following pheromone. Numerous electron-lucent droplets and large channels containing lipid micelles are found in the cytoplasm here, but the channels cannot be traced out of the secretory layer. The third layer consists of large pyriform cells. The campaniform sensilla are composed of three cells: the sensory cell proper whose dendrite carries a modified 9 + 0 sensory process, an accessory supporting cell that secretes an electron-opaque sheath, and an enveloping cell. At the cell borders of the sensillum, regions of septate and tight junction appear. There are also septate junctions between columnar cells and possibly tight junctions between columnar and secretory cells that would open an intracellular and molecular pathway to the endocuticle. The campaniform sensilla may be part of a feedback control system that determines the amount of pheromone deposited during trail laying.

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Selected References

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  1. BRIGHTMAN M. W., PALAY S. L. THE FINE STRUCTURE OF EPENDYMA IN THE BRAIN OF THE RAT. J Cell Biol. 1963 Nov;19:415–439. doi: 10.1083/jcb.19.2.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Gupta B. L., Berridge M. J. Fine structural organization of the rectum in the blowfly, Calliphora erythrocephala (Meig.) with special reference to connective tissue, tracheae and neurosecretory innervation in the rectal papillae. J Morphol. 1966 Sep;120(1):23–81. doi: 10.1002/jmor.1051200104. [DOI] [PubMed] [Google Scholar]
  3. Happ G. M., Strandberg J. D., Happ C. M. The terpene-producing glands of a Phasmid insect. Cell morphology and histochemistry. J Morphol. 1966 Jun;119(2):143–160. doi: 10.1002/jmor.1051190204. [DOI] [PubMed] [Google Scholar]
  4. Hoye A. Purification of insulin labelled with iodine-131. Nature. 1966 Aug 13;211(5050):746–746. doi: 10.1038/211746a0. [DOI] [PubMed] [Google Scholar]
  5. KANNO Y., LOEWENSTEIN W. R. INTERCELLULAR DIFFUSION. Science. 1964 Feb 28;143(3609):959–960. doi: 10.1126/science.143.3609.959. [DOI] [PubMed] [Google Scholar]
  6. LOCKE M. PERMEABILITY OF INSECT CUTICLE TO WATER AND LIPIDS. Science. 1965 Jan 15;147(3655):295–298. [PubMed] [Google Scholar]
  7. LOCKE M. Pore canals and related structures in insect cuticle. J Biophys Biochem Cytol. 1961 Aug;10:589–618. doi: 10.1083/jcb.10.4.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LOCKE M. THE STRUCTURE OF SEPTATE DESMOSOMES. J Cell Biol. 1965 Apr;25:166–169. doi: 10.1083/jcb.25.1.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. 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]
  11. ROTH T. F., PORTER K. R. YOLK PROTEIN UPTAKE IN THE OOCYTE OF THE MOSQUITO AEDES AEGYPTI. L. J Cell Biol. 1964 Feb;20:313–332. doi: 10.1083/jcb.20.2.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SATIR P., STUART A. M. A NEW APICAL MICROTUBULE-ASSOCIATED ORGANELLE IN THE STERNAL GLAND OF ZOOTERMOPSIS NEVADENSIS (HAGEN), ISOPTERA. J Cell Biol. 1965 Feb;24:277–283. doi: 10.1083/jcb.24.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. SLIFER E. H., SEKHON S. S. FINE STRUCTURE OF THE SENSE ORGANS ON THE ANTENNAL FLAGELLUM OF A FLESH FLY, SARCOPHAGA ARGYROSTOMA R.-D. (DIPTERA, SARCOPHAGIDAE). J Morphol. 1964 Jan;114:185–207. doi: 10.1002/jmor.1051140107. [DOI] [PubMed] [Google Scholar]
  14. SLIFER E. H., SEKHON S. S. THE DENDRITES OF THE THIN-WALLED OLFACTORY PEGS OF THE GRASSHOPPER (ORTHOPTERA, ACRIDIDAE). J Morphol. 1964 May;114:393–409. doi: 10.1002/jmor.1051140303. [DOI] [PubMed] [Google Scholar]
  15. THURM U. MECHANORECEPTORS IN THE CUTICLE OF THE HONEY BEE: FINE STRUCTURE AND STIMULUS MECHANISM. Science. 1964 Sep 4;145(3636):1063–1065. doi: 10.1126/science.145.3636.1063. [DOI] [PubMed] [Google Scholar]
  16. WIENER J., SPIRO D., LOEWENSTEIN W. R. STUDIES ON AN EPITHELIAL (GLAND) CELL JUNCTION. II. SURFACE STRUCTURE. J Cell Biol. 1964 Sep;22:587–598. doi: 10.1083/jcb.22.3.587. [DOI] [PMC free article] [PubMed] [Google Scholar]

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