The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Calcium-induced asymmetrical beating of triton-demembranated sea urchin sperm flagella.
Open accessAbstract
Asymmetrical bending waves can be obtained by reactivating demembranated sea urchin spermatozoa at high Ca2+ concentrations. Moving-film flash photography shows that asymmetrical flagellar bending waves are associated with premature termination of the growth of the bends in one direction (the reverse bends) while the bends in the opposite direction (the principal bends) grow for one full beat cycle, and with unequal rates of growth of principal and reverse bends. The relative proportions of these two components of asymmetry are highly variable. The increased angle in the principal bend is compensated by a decreased angle in the reverse bend, so that there is no change in mean bend angle; the wavelength and beat frequency are also independent of the degree of asymmetry. This new information is still insufficient to identify a particular mechanism for Ca2+-induced asymmetry. When a developing bend stops growing before initiation of growth of a new bend in the same direction, a modification of the sliding between tubules in the distal portion of the flagellum is required. This modification can be described as a superposition of synchronous sliding on the metachronous sliding associated with propagating bending waves. Synchronous sliding is particularly evident in highly asymmetrical flagella, but is probably not the cause of asymmetry. The control of metachronous sliding appears to be unaffected by the superposition of synchronous sliding.
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Citations
Cites
Adenosine Triphosphate-Induced Sliding of Tubules in Trypsin-Treated Flagella of Sea-Urchin Sperm
Summers, K. E., & Gibbons, I. R. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.12.3092 · Cited by 697
Gibbons, B. H., & Gibbons, I. R. (1972) · The Journal of Cell Biology · doi:10.1083/jcb.54.1.75 · Cited by 570
Satir, P. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.39.1.77 · Cited by 555
Reactivated Triton-Extracted Models of Paramecium : Modification of Ciliary Movement by Calcium Ions
Naitoh, Y., & Kaneko, H. (1972) · Science · doi:10.1126/science.176.4034.523 · Cited by 442
THE STRUCTURAL BASIS OF CILIARY BEND FORMATION
Warner, F. D., & Satir, P. (1974) · The Journal of Cell Biology · doi:10.1083/jcb.63.1.35 · Cited by 348
Direction of active sliding of microtubules in Tetrahymena cilia.
Sale, W. S., & Satir, P. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.5.2045 · Cited by 320
Hyams, J. S., & Borisy, G. G. (1978) · Journal of Cell Science · doi:10.1242/jcs.33.1.235 · Cited by 313
Calcium ion regulation of flagellar beat symmetry in reactivated sea urchin spermatozoa
Brokaw, C. J., Josslin, R., & Bobrow, L. (1974) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(74)80487-0 · Cited by 211
Self-citationComputer Simulation of Flagellar Movement
Brokaw, C. J. (1972) · Biophysical Journal · doi:10.1016/s0006-3495(72)86104-6 · Cited by 206
Self-citationBrokaw, C. J. (1972) · Science · doi:10.1126/science.178.4060.455 · Cited by 195
Self-citation
Cited by
CatSper1 required for evoked Ca 2+ entry and control of flagellar function in sperm
Carlson, A. E., Westenbroek, R. E., Quill, T., Ren, D., Clapham, D. E., Hille, B., Garbers, D. L., & Babcock, D. F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2536658100 · Cited by 379
Friedrich, B. M., & Jülicher, F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703530104 · Cited by 287
Sperm flagella: comparative and phylogenetic perspectives of protein components
Inaba, K. (2011) · Molecular Human Reproduction · doi:10.1093/molehr/gar034 · Cited by 287
Mechanisms of sperm chemotaxis
Kaupp, U. B., Kashikar, N. D., & Weyand, I. (2008) · Annual Review of Physiology · doi:10.1146/annurev.physiol.70.113006.100654 · Cited by 284
Friedrich, B. M., Riedel-Kruse, I. H., Howard, J., & Jülicher, F. (2010) · Journal of Experimental Biology · doi:10.1242/jeb.039800 · Cited by 276
Metadata
- Authors
- Brokaw, C. J.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1979-08-01
- Volume
- 82
- Issue
- 2
- Pages
- 401-411
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2053842210
- Cited by
- 272
- References
- 17
- FWCI
- 4.10
- Type
- journal article
- Language
- en
- Open access
- green
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.