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. 1970 Aug 1;46(2):220–234. doi: 10.1083/jcb.46.2.220

THE EFFECTS OF COLCHICINE ON SPERMATOGENESIS IN NITELLA

F Rudolf Turner 1
PMCID: PMC2108012  PMID: 5465156

Abstract

Treatment of Nitella antheridia with colchicine results in various sperm abnormalities, depending upon duration of exposure and subsequent recovery. Early effects of treatment include disappearance of spindle fibers and a cessation of ordered cell wall formation in dividing cells. Sperm released from antheridia treated for 24 hr and allowed to recover for 4–5 days possess branched flagella. After a recovery period of 6–10 days the sperm appear normal; however, following longer recovery periods, the sperm exhibit variations in size and number of flagella. Branched flagella contain a variety of microtubule patterns ranging from branches containing a single microtubule to flagella with an excess of microtubules. Spermatids which differentiate in the presence of colchicine lack flagella and a microtubular sheath. Nuclear contents undergo condensation stages; however, the nucleus as a whole does not undergo the orderly elongation and coiling characteristic of untreated Nitella spermatids. Long-term colchicine treatment followed by a recovery period produces atypical microtubules and microtubular aggregations in the spermatid. The results indicate that colchicine affects not only polymerization of microtubule subunits but also factors responsible for their ordered spatial relationships in the cell. The presence of microtubules is a prerequisite for normal morphological changes during spermiogenesis.

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Selected References

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

  1. Behnke O., Forer A. Evidence for four classes of microtubules in individual cells. J Cell Sci. 1967 Jun;2(2):169–192. doi: 10.1242/jcs.2.2.169. [DOI] [PubMed] [Google Scholar]
  2. Borisy G. G., Taylor E. W. The mechanism of action of colchicine. Binding of colchincine-3H to cellular protein. J Cell Biol. 1967 Aug;34(2):525–533. doi: 10.1083/jcb.34.2.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Borisy G. G., Taylor E. W. The mechanism of action of colchicine. Colchicine binding to sea urchin eggs and the mitotic apparatus. J Cell Biol. 1967 Aug;34(2):535–548. doi: 10.1083/jcb.34.2.535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brinkley B. R., Stubblefield E., Hsu T. C. The effects of colcemid inhibition and reversal on the fine structure of the mitotic apparatus of Chinese hamster cells in vitro. J Ultrastruct Res. 1967 Jul;19(1):1–18. doi: 10.1016/s0022-5320(67)80057-1. [DOI] [PubMed] [Google Scholar]
  5. Cronshaw J., Bouck G. B. THE FINE STRUCTURE OF DIFFERENTIATING XYLEM ELEMENTS. J Cell Biol. 1965 Mar 1;24(3):415–431. doi: 10.1083/jcb.24.3.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Inoué S., Sato H. Cell motility by labile association of molecules. The nature of mitotic spindle fibers and their role in chromosome movement. J Gen Physiol. 1967 Jul;50(6 Suppl):259–292. [PMC free article] [PubMed] [Google Scholar]
  7. Kleinfeld R. G., Sisken J. E. Morphological and kinetic aspects of mitotic arrest by and recovery from colcemid. J Cell Biol. 1966 Dec;31(3):369–379. doi: 10.1083/jcb.31.3.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ledbetter M. C., Porter K. R. A "MICROTUBULE" IN PLANT CELL FINE STRUCTURE. J Cell Biol. 1963 Oct 1;19(1):239–250. doi: 10.1083/jcb.19.1.239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. MOLLENHAUER H. H. PLASTIC EMBEDDING MIXTURES FOR USE IN ELECTRON MICROSCOPY. Stain Technol. 1964 Mar;39:111–114. [PubMed] [Google Scholar]
  10. ROBBINS E., GONATAS N. K. HISTOCHEMICAL AND ULTRASTRUCTURAL STUDIES ON HELA CELL CULTURES EXPOSED TO SPINDLE INHIBITORS WITH SPECIAL REFERENCE TO THE INTERPHASE CELL. J Histochem Cytochem. 1964 Sep;12:704–711. doi: 10.1177/12.9.704. [DOI] [PubMed] [Google Scholar]
  11. Rosenbaum J. L., Carlson K. Cilia regeneration in Tetrahymena and its inhibition by colchicine. J Cell Biol. 1969 Feb;40(2):415–425. doi: 10.1083/jcb.40.2.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Rosenbaum J. L., Child F. M. Flagellar regeneration in protozoan flagellates. J Cell Biol. 1967 Jul;34(1):345–364. doi: 10.1083/jcb.34.1.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. 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]
  14. Shelanski M. L., Taylor E. W. Isolation of a protein subunit from microtubules. J Cell Biol. 1967 Aug;34(2):549–554. doi: 10.1083/jcb.34.2.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Stubblefield E., Brinkley B. R. Cilia formation in Chinese hamster fibroblasts in vitro as a response to colcemid treatment. J Cell Biol. 1966 Sep;30(3):645–652. doi: 10.1083/jcb.30.3.645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Tilney L. G., Gibbins J. R. Differential effects of antimitotic agents on the stability and behavior of cytoplasmic and ciliary microtubules. Protoplasma. 1968;65(1):167–179. doi: 10.1007/BF01666377. [DOI] [PubMed] [Google Scholar]
  17. Tilney L. G., Gibbins J. R. Microtubules in the formation and development of the primary mesenchyme in Arbacia punctulata. II. An experimental analysis of their role in development and maintenance of cell shape. J Cell Biol. 1969 Apr;41(1):227–250. doi: 10.1083/jcb.41.1.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Tilney L. G. Studies on the microtubules in heliozoa. IV. The effect of colchicine on the formation and maintenance of the axopodia and the redevelopment of pattern in Actinosphaerium nucleofilum (Barrett). J Cell Sci. 1968 Dec;3(4):549–562. doi: 10.1242/jcs.3.4.549. [DOI] [PubMed] [Google Scholar]
  19. Turner F. R. An ultrastructural study of plant spermatogenesis. Spermatogenesis in Nitella. J Cell Biol. 1968 May;37(2):370–393. doi: 10.1083/jcb.37.2.370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. WOODING F. B., NORTHCOTE D. H. THE DEVELOPMENT OF THE SECONDARY WALL OF THE XYLEM IN ACER PSEUDOPLATANUS. J Cell Biol. 1964 Nov;23:327–337. doi: 10.1083/jcb.23.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Wanka F. Ultrastructural changes during normal and colchicine-inhibited cell division of Chlorella. Protoplasma. 1968;66(1):105–130. doi: 10.1007/BF01252527. [DOI] [PubMed] [Google Scholar]
  22. Whaley W. G., Dauwalder M., Kephart J. E. The Golgi apparatus and an early stage in cell plate formation. J Ultrastruct Res. 1966 Apr;15(1):169–180. doi: 10.1016/s0022-5320(66)80102-8. [DOI] [PubMed] [Google Scholar]
  23. Wisniewski H., Shelanski M. L., Terry R. D. Effects of mitotic spindle inhibitors on neurotubules and neurofilaments in anterior horn cells. J Cell Biol. 1968 Jul;38(1):224–229. doi: 10.1083/jcb.38.1.224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Zucker-Franklin D. Microfibrils of blood platelets: their relationship TO MICROTUBULES AND THE CONTRACTILE PROTEIN. J Clin Invest. 1969 Jan;48(1):165–175. doi: 10.1172/JCI105965. [DOI] [PMC free article] [PubMed] [Google Scholar]

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