» Articles » PMID: 1894694

Microtubule Sliding in Swimming Sperm Flagella: Direct and Indirect Measurements on Sea Urchin and Tunicate Spermatozoa

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1991 Sep 1
PMID 1894694
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Direct measurements of microtubule sliding in the flagella of actively swimming, demembranated, spermatozoa have been made using submicron diameter gold beads as markers on the exposed outer doublet microtubules. With spermatozoa of the tunicate, Ciona, these measurements confirm values of sliding calculated indirectly by measuring angles relative to the axis of the sperm head. Both methods of measurement show a nonuniform amplitude of oscillatory sliding along the length of the flagellum, providing direct evidence that "oscillatory synchronous sliding" can be occurring in the flagellum, in addition to the metachronous sliding that is necessary to propagate a bending wave. Propagation of constant amplitude bends is not accomplished by propagation of a wave of oscillatory sliding of constant amplitude, and therefore appears to require a mechanism for monitoring and controlling the bend angle as bends propagate. With sea urchin spermatozoa, the direct measurements of sliding do not agree with the values calculated by measuring angles relative to the head axis. The oscillation in angular orientation of the sea urchin sperm head as it swims appears to be accommodated by flexure at the head-flagellum junction and does not correspond to oscillation in orientation of the basal end of the flagellum. Consequently, indirect calculations of sliding based on angles measured relative to the longitudinal axis of the sperm head can be seriously inaccurate in this species.

Citing Articles

Analysing the motion of scallop-like swimmers in a noisy environment.

Patil G, Ghosh A Eur Phys J Spec Top. 2023; 232(6):927-933.

PMID: 37309448 PMC: 7614634. DOI: 10.1140/epjs/s11734-022-00728-x.


Effects of continuous and discrete boundary conditions on the movement of upper-convected maxwell and Newtonian mucus layers in coughing and sneezing.

Modaresi M, Shirani E Eur Phys J Plus. 2022; 137(7):846.

PMID: 35892063 PMC: 9302954. DOI: 10.1140/epjp/s13360-022-03067-x.


Composition and function of ciliary inner-dynein-arm subunits studied in Chlamydomonas reinhardtii.

Yamamoto R, Hwang J, Ishikawa T, Kon T, Sale W Cytoskeleton (Hoboken). 2021; 78(3):77-96.

PMID: 33876572 PMC: 8217317. DOI: 10.1002/cm.21662.


The many modes of flagellar and ciliary beating: Insights from a physical analysis.

Lindemann C, Lesich K Cytoskeleton (Hoboken). 2021; 78(2):36-51.

PMID: 33675288 PMC: 8048621. DOI: 10.1002/cm.21656.


The Kinetics of Nucleotide Binding to Isolated Chlamydomonas Axonemes Using UV-TIRF Microscopy.

Feofilova M, Mahamdeh M, Howard J Biophys J. 2019; 117(4):679-687.

PMID: 31400919 PMC: 6712413. DOI: 10.1016/j.bpj.2019.07.004.


References
1.
Goldstein S . Form of developing bends in reactivated sperm flagella. J Exp Biol. 1976; 64(1):173-84. DOI: 10.1242/jeb.64.1.173. View

2.
Sale W . The axonemal axis and Ca2+-induced asymmetry of active microtubule sliding in sea urchin sperm tails. J Cell Biol. 1986; 102(6):2042-52. PMC: 2114254. DOI: 10.1083/jcb.102.6.2042. View

3.
Satir P . Studies on cilia. 3. Further studies on the cilium tip and a "sliding filament" model of ciliary motility. J Cell Biol. 1968; 39(1):77-94. PMC: 2107504. DOI: 10.1083/jcb.39.1.77. View

4.
Brokaw C . Computerized analysis of flagellar motility by digitization and fitting of film images with straight segments of equal length. Cell Motil Cytoskeleton. 1990; 17(4):309-16. DOI: 10.1002/cm.970170406. View

5.
Gibbons I . Transient flagellar waveforms in reactivated sea urchin sperm. J Muscle Res Cell Motil. 1986; 7(3):245-50. DOI: 10.1007/BF01753557. View