Abstract
This study evidence for tension transmission by microtubules and desmosomes in the follicular epithelium during anisometric growth of certain insect eggs. Most insect oocytes, and the follicles which surround them, grow anisometrically as they assume shapes which approximate to those of long prolate spheroids. Surface growth is most rapid in directions which parallel the polar axis of an oocyte and slowest in circumferential directions at right angles to this axis. The longitudinal axes of microtubule bundles in follicle cells of the gall midge Heteropeza and the cockroach Periplaneta are oriented circumferentially with respect to the surfaces of developing eggs and at right angles to the polar axes of eggs. At cell boundaries, the tubules appear to be attached to spot desmosomes. It is suggested that microtubules and desmosomes form a mechanical continuum throughout a follicular epithelium which transmits tensile forces around the circumference of a growing egg. Follicular resistance to circumferential expansion may be largely responsible for defining the elongate form of insect eggs.
Full Text
The Full Text of this article is available as a PDF (2.7 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ANDERSON E. OOCYTE DIFFERENTIATION AND VITELLOGENESIS IN THE ROACH PERIPLANETA AMERICANA. J Cell Biol. 1964 Jan;20:131–155. doi: 10.1083/jcb.20.1.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BYERS B., PORTER K. R. ORIENTED MICROTUBULES IN ELONGATING CELLS OF THE DEVELOPING LENS RUDIMENT AFTER INDUCTION. Proc Natl Acad Sci U S A. 1964 Oct;52:1091–1099. doi: 10.1073/pnas.52.4.1091. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown D. L., Bouck G. B. Microtubule biogenesis and cell shape in Ochromonas. II. The role of nucleating sites in shape development. J Cell Biol. 1973 Feb;56(2):360–378. doi: 10.1083/jcb.56.2.360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burnside B. Microtubules and microfilaments in newt neuralation. Dev Biol. 1971 Nov;26(3):416–441. doi: 10.1016/0012-1606(71)90073-x. [DOI] [PubMed] [Google Scholar]
- Burnside B. The form and arrangement of microtubules: an historical, primarily morphological, review. Ann N Y Acad Sci. 1975 Jun 30;253:14–26. doi: 10.1111/j.1749-6632.1975.tb19189.x. [DOI] [PubMed] [Google Scholar]
- CORLISS J. O. Silver impregnation of ciliated protozoa by the Chatton-Lwoff technic. Stain Technol. 1953 Mar;28(2):97–100. doi: 10.3109/10520295309105108. [DOI] [PubMed] [Google Scholar]
- Caveney S. Muscle attachment related to cuticle architecture in Apterygota. J Cell Sci. 1969 Mar;4(2):541–559. doi: 10.1242/jcs.4.2.541. [DOI] [PubMed] [Google Scholar]
- Fawcett D. W., McNutt N. S. The ultrastructure of the cat myocardium. I. Ventricular papillary muscle. J Cell Biol. 1969 Jul;42(1):1–45. doi: 10.1083/jcb.42.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fullilove S. L., Jacobson A. G. Nuclear elongation and cytokinesis in Drosophila montana. Dev Biol. 1971 Dec;26(4):560–577. doi: 10.1016/0012-1606(71)90141-2. [DOI] [PubMed] [Google Scholar]
- Fux T. Chromosome elimination in Heteropeza pygmaea. II. Ultrastructure of the spindle apparatus. Chromosoma. 1974;49(1):99–112. doi: 10.1007/BF00284991. [DOI] [PubMed] [Google Scholar]
- Handel M. A., Roth L. E. Cell shape and morphology of the neural tube: implications for microtubule function. Dev Biol. 1971 May;25(1):78–95. doi: 10.1016/0012-1606(71)90020-0. [DOI] [PubMed] [Google Scholar]
- Mahowald A. P. Ultrastructural observations on oogenesis in Drosophila. J Morphol. 1972 May;137(1):29–48. doi: 10.1002/jmor.1051370103. [DOI] [PubMed] [Google Scholar]
- Mooseker M. S., Tilney L. G. Isolation and reactivation of the axostyle. Evidence for a dynein-like ATPase in the axostyle. J Cell Biol. 1973 Jan;56(1):13–26. doi: 10.1083/jcb.56.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ockleford C. D., Tucker J. B. Growth, breakdown, repair, and rapid contraction of microtubular axopodia in the heliozoan Actinophrys sol. J Ultrastruct Res. 1973 Sep;44(5):369–387. doi: 10.1016/s0022-5320(73)90005-1. [DOI] [PubMed] [Google Scholar]
- Ockleford C. K. Cytokinesis in the heliozoan Actinophrys sol. J Cell Sci. 1974 Dec;16(3):499–517. doi: 10.1242/jcs.16.3.499. [DOI] [PubMed] [Google Scholar]
- Piatigorsky J. Lens cell elongation in vitro and microtubules. Ann N Y Acad Sci. 1975 Jun 30;253:333–347. doi: 10.1111/j.1749-6632.1975.tb19211.x. [DOI] [PubMed] [Google Scholar]
- Sanger J. M., Jackson W. T. Fine structure study of pollen development in Haemanthus katherinae Baker. II. Microtubules and elongation of the generative cells. J Cell Sci. 1971 Mar;8(2):303–315. doi: 10.1242/jcs.8.2.303. [DOI] [PubMed] [Google Scholar]
- Staehelin L. A. Structure and function of intercellular junctions. Int Rev Cytol. 1974;39:191–283. doi: 10.1016/s0074-7696(08)60940-7. [DOI] [PubMed] [Google Scholar]
- Summers K. E., Gibbons I. R. Adenosine triphosphate-induced sliding of tubules in trypsin-treated flagella of sea-urchin sperm. Proc Natl Acad Sci U S A. 1971 Dec;68(12):3092–3096. doi: 10.1073/pnas.68.12.3092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Tucker J. B. Changes in nuclear structure during binary fission in the ciliate Nassula. J Cell Sci. 1967 Dec;2(4):481–498. doi: 10.1242/jcs.2.4.481. [DOI] [PubMed] [Google Scholar]
- Tucker J. B. Fine structure and function of the cytopharyngeal basket in the ciliate Nassula. J Cell Sci. 1968 Dec;3(4):493–514. doi: 10.1242/jcs.3.4.493. [DOI] [PubMed] [Google Scholar]
- Tucker J. B. Microtubule arms and cytoplasmic streaming and microtubule bending and stretching of intertubule links in the feeding tentacle of the suctorian ciliate Tokophrya. J Cell Biol. 1974 Aug;62(2):424–437. doi: 10.1083/jcb.62.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warren R. H. Microtubular organization in elongating myogenic cells. J Cell Biol. 1974 Nov;63(2 Pt 1):550–566. doi: 10.1083/jcb.63.2.550. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warren R. H. The effect of colchicine on myogenesis in vivo in Rana pipiens and Rhodnius prolixus (Hemiptera). J Cell Biol. 1968 Dec;39(3):544–555. doi: 10.1083/jcb.39.3.544. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Went D. F. In vitro culture of eggs and embryos of the viviparous paedogenetic gallmidge Heteropeza pygmaea. J Exp Zool. 1971 Jul;177(3):301–311. doi: 10.1002/jez.1401770304. [DOI] [PubMed] [Google Scholar]