Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1971 Jan 1;48(1):61–78. doi: 10.1083/jcb.48.1.61

THE ORIGIN AND FATE OF MICROBODIES IN THE FAT BODY OF AN INSECT

M Locke 1, J T McMahon 1
PMCID: PMC2108215  PMID: 4322718

Abstract

The structure and life history of insect microbodies are described during the development of the fat body from the 4th to 5th larval molt through the 5th to pupal molt. The mature microbodies are flattened spheres about 1.1 x 0.9 µ, with a depression on one side where a dense mass connects the limiting membrane to the core of coiled tubules. They contain catalase and urate oxidase. The precise synchrony of development of insect cells during the molt/intermolt cycle makes it easy to study the life history of particular organelles. Phases of growth are correlated with the hormonal milieu. Mature 4th stage microbodies decrease in size before ecdysis to the 5th stage when they atrophy at the same time as the new 5th stage generation arises. The 5th stage microbodies form as diverticula of the RER and, grow while confronted by RER cisternae. The mature microbodies decrease in size when the fat body engages in massive larval syntheses. At the end of the 5th larval stage, the microbodies are invested by isolation membranes and destroyed before pupation. There are thus two mechanisms for microbody destruction: atrophy of the 4th stage organelles and isolation with autophagy at the end of the 5th stage.

Full Text

The Full Text of this article is available as a PDF (2.2 MB).

Selected References

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

  1. Beard M. E., Novikoff A. B. Distribution of peroxisomes (microbodies) in the nephron of the rat: a cytochemical study. J Cell Biol. 1969 Aug;42(2):501–518. doi: 10.1083/jcb.42.2.501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brown A. W. The nitrogen metabolism of an insect (Lucilia sericata Mg.): Uric acid, allantoin and uricase. Biochem J. 1938 May;32(5):895–902. doi: 10.1042/bj0320895. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. De Duve C., Baudhuin P. Peroxisomes (microbodies and related particles). Physiol Rev. 1966 Apr;46(2):323–357. doi: 10.1152/physrev.1966.46.2.323. [DOI] [PubMed] [Google Scholar]
  4. De Duve C., Wattiaux R. Functions of lysosomes. Annu Rev Physiol. 1966;28:435–492. doi: 10.1146/annurev.ph.28.030166.002251. [DOI] [PubMed] [Google Scholar]
  5. Fahimi H. D. Cytochemical localization of peroxidase activity in rat hepatic microbodies (peroxisomes). J Histochem Cytochem. 1968 Aug;16(8):547–550. doi: 10.1177/16.8.547. [DOI] [PubMed] [Google Scholar]
  6. Farquhar M. G., Palade G. E. Cell junctions in amphibian skin. J Cell Biol. 1965 Jul;26(1):263–291. doi: 10.1083/jcb.26.1.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Goldfischer S., Essner E. Further observations on the peroxidatic activities of microbodies (Peroxisomes). J Histochem Cytochem. 1969 Oct;17(10):681–685. doi: 10.1177/17.10.681. [DOI] [PubMed] [Google Scholar]
  8. Graham R. C., Jr, Karnovsky M. J. The histochemical demonstration of uricase activity. J Histochem Cytochem. 1965 Jul-Aug;13(6):448–453. doi: 10.1177/13.6.448. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Locke M., Collins J. V. Protein uptake in multivesicular bodies in the molt-intermolt cycle of an insect. Science. 1967 Jan 27;155(3761):467–469. doi: 10.1126/science.155.3761.467. [DOI] [PubMed] [Google Scholar]
  11. Locke M., Collins J. V. Protein uptake into multivesicular bodies and storage granules in the fat body of an insect. J Cell Biol. 1968 Mar;36(3):453–483. doi: 10.1083/jcb.36.3.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Novikoff A. B., Goldfischer S. Visualization of peroxisomes (microbodies) and mitochondria with diaminobenzidine. J Histochem Cytochem. 1969 Oct;17(10):675–680. doi: 10.1177/17.10.675. [DOI] [PubMed] [Google Scholar]
  13. Poole B., Leighton F., De Duve C. The synthesis and turnover of rat liver peroxisomes. II. Turnover of peroxisome proteins. J Cell Biol. 1969 May;41(2):536–546. doi: 10.1083/jcb.41.2.536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. 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]
  15. Strum J. M., Karnovsky M. J. Cytochemical localization of endogenous peroxidase in thyroid follicular cells. J Cell Biol. 1970 Mar;44(3):655–666. doi: 10.1083/jcb.44.3.655. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Tsukada H., Mochizuki Y., Konishi T. Morphogenesis and development of microbodies of hepatocytes of rats during pre- and postnatal growth. J Cell Biol. 1968 May;37(2):231–243. doi: 10.1083/jcb.37.2.231. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES