The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
STUDIES ON CILIA
Open accessAbstract
This study confirms and extends previous work on the lateral cilia of the fresh-water mussel, Elliptio complanatus, in support of a "sliding filament" mechanism of ciliary motility wherein peripheral filaments (microtubules) do not change length during beat (see Satir, 1967). Short sequences of serial sections of tips are examined in control (nonbeating) and activated (metachronal wave) preparations. Several different tip types, functional rather than morphogenetic variants, are demonstrated, but similarly bent cilia have similar tips. The peripheral filaments are composed of two subfibers: a and b. The bent regions of cilia are in the form of circular arcs, and apparent differences in subfiber-b length at the tip are those predicted solely by geometry of the stroke without the necessity of assuming filament contraction. Various subfibers b apparently move with respect to one another during beat, since small systematic variations in relative position can be detected from cilium to cilium. While subfiber-b lengths are uniform throughout, subfiber-a lengths are morphologically different for each filament: 8 and 3 are about 0.8 µ longer than 1, 4 and 5, but each unique length is independent of stroke position or tip type. Subfiber-a does not contract, nor does it move, e.g. slide, with respect to subfiber-b of the same doublet. The central pair of filaments extends to the tip of the cilium where its members fuse. Subunit assembly in ciliary microtubules is evidently precise. This may be of importance in establishing the relationships needed for mechanochemical interactions that produce sliding and beat.
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Cites
Cell Motility by Labile Association of Molecules
Inoué, S., & Sato, H. (1967) · The Journal of General Physiology · doi:10.1085/jgp.50.6.259 · Cited by 757
Electron Microscopy of the Sperm Tail Results Obtained with a New Fixative
Afzelius, B. (1959) · The Journal of Cell Biology · doi:10.1083/jcb.5.2.269 · Cited by 498
Peachey, L. D. (1958) · The Journal of Cell Biology · doi:10.1083/jcb.4.3.233 · Cited by 335
Satir, P. (1965) · The Journal of Cell Biology · doi:10.1083/jcb.26.3.805 · Cited by 229
Self-citationStudies on the Adenosine Triphosphatase Activity of 14 S and 30 S Dynein from Cilia of Tetrahymena
Gibbons, I. R. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96385-4 · Cited by 195
Adenosine Triphosphate Usage by Flagella
Brokaw, C. J. (1967) · Science · doi:10.1126/science.156.3771.76 · Cited by 76
SUBSTRUCTURE OF FLAGELLAR TUBULES
Phillips, D. M. (1966) · The Journal of Cell Biology · doi:10.1083/jcb.31.3.635 · Cited by 67
Cited by
Lighthill, J. (1976) · SIAM Review · doi:10.1137/1018040 · Cited by 738
Nasal mucociliary clearance as a factor in nasal drug delivery
Marttin, E., Schipper, N. G. M., Verhoef, J. C., & Merkus, F. W. H. M. (1998) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(97)00059-8 · Cited by 469
Wallmeier, J., Nielsen, K. G., Kuehni, C. E., Lucas, J. S., Leigh, M. W., Zariwala, M. A., & Omran, H. (2020) · Nature Reviews Disease Primers · doi:10.1038/s41572-020-0209-6 · Cited by 403
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
Self-citationA cross-bridge model of muscle contraction
Eisenberg, E., & Hill, T. L. (1979) · Progress in Biophysics and Molecular Biology · doi:10.1016/0079-6107(79)90025-7 · Cited by 314
Metadata
- Authors
- Satir, P.
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 1968-10-01
- Volume
- 39
- Issue
- 1
- Pages
- 77-94
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2746196359
- Cited by
- 555
- References
- 7
- FWCI
- 11.62
- Type
- journal article
- Language
- en
- Open access
- green
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