Abstract
The long slender retinal cones of fishes shorten in the light and elongate in the dark. Light-induced cone shortening provides a useful model for stuying nonmuscle contraction because it is linear, slow, and repetitive. Cone cells contain both thin (actin) and thick (myosinlike) filaments oriented parallel to the axis of contraction. This study examines the polarities of the cone's thin filaments and the changes in filament distribution which accompany light-induced contraction, in an attempt to elucidate the structural basis for the cone's contractile process. The proximal half of the cone is fixed to its cellular neighbors in the outer nuclear layer while the distal half is free. Thus, all shortening takes place in a necklike region (the myoid) in the distal half of the cone which extends into the space between the neural retina and the pigmented retinal epithelium. Thin filaments are found throughout the length of the cone, whereas thick filaments occur predominantly in the proximal (axon) regions of both light- and dark- adapted cones. Thus, thick filaments are primarily localized outside the region where shortening takes place. Observations from myosin subfragment-1 binding studies suggest that the cone's thin filaments are organized into two opposing sets. In the distal half of the cone (including the myoid), virtually all filaments have proximally directed arrowheads. In the more proximal regions of the axon, many thin filaments have opposite polarity, their arrowheads being distally directed. Near the synaptic proximal end of the light-adapted (contracted) cone, filaments of opposite polarities occur in approximately equal numbers. Thus, in the cone axon there appear to be two overlapping sets of actin filaments whose opposite polarities correspond to the two actin halves of a muscle sarcomere. In elongated, dark-adapted cones, thick filaments are localized throughout the axon region of the cone. In light, thick filaments accumulate towards the proximal end of the cone. These observations are consistent with a "sliding hypothesis" for cone contraction, in which thick myosinlike filaments produce sliding interdigitation of the two sets of oppositely directed actin filaments in the proximal axon region. Thus, the myoid thin filaments would be essentially reeled into the axon region to produce shortening. The mechanism of re-elongation depends on microtubules, as discussed in the companion paper.
Full Text
The Full Text of this article is available as a PDF (5.7 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bhowmick D. K. Electron microscopy of Trichamoeba villosa and amoeboid movement. Exp Cell Res. 1967 Mar;45(3):570–589. doi: 10.1016/0014-4827(67)90161-9. [DOI] [PubMed] [Google Scholar]
- Bois R. M., Pease D. C. Electron microscopic studies of the state of myosin aggregation in the vertebrate smooth muscle cell. Anat Rec. 1974 Nov;180(3):465–479. doi: 10.1002/ar.1091800306. [DOI] [PubMed] [Google Scholar]
- Buckley I. K. Subcellular motility: a correlated light and electron microscopic study using cultured cells. Tissue Cell. 1974;6(1):1–20. doi: 10.1016/0040-8166(74)90019-6. [DOI] [PubMed] [Google Scholar]
- Burnside B., Laties A. M. Actin filaments in apical projections of the primate pigmented epithelial cell. Invest Ophthalmol. 1976 Jul;15(7):570–575. [PubMed] [Google Scholar]
- Burnside B. Microtubules and actin filaments in teleost visual cone elongation and contraction. J Supramol Struct. 1976;5(3):257–275. doi: 10.1002/jss.400050302. [DOI] [PubMed] [Google Scholar]
- Burnside M. B. Possible roles of microtubules and actin filaments in retinal pigmented epithelium. Exp Eye Res. 1976 Aug;23(2):257–275. doi: 10.1016/0014-4835(76)90208-6. [DOI] [PubMed] [Google Scholar]
- Hartwig J. H., Stossel T. P. Interactions of actin, myosin, and an actin-binding protein of rabbit pulmonary macrophages. III. Effects of cytochalasin B. J Cell Biol. 1976 Oct;71(1):295–303. doi: 10.1083/jcb.71.1.295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kessler D. On the location of myosin in the myxomycete Physarum polycephalum and its possible function in cytoplasmic streaming. J Mechanochem Cell Motil. 1972 Aug;1(3):125–137. [PubMed] [Google Scholar]
- Lowy J., Small J. V. The organization of myosin and actin in vertebrate smooth muscle. Nature. 1970 Jul 4;227(5253):46–51. doi: 10.1038/227046a0. [DOI] [PubMed] [Google Scholar]
- Malawista S. E., Gee J. B., Bensch K. G. Cytochalasin B reversibly inhibits phagocytosis: functional, metabolic, and ultrastructural effects in human blood leukocytes and rabbit alveolar macrophages. Yale J Biol Med. 1971 Dec;44(3):286–300. [PMC free article] [PubMed] [Google Scholar]
- Miller W. H., Snyder A. W. Optical function of myoids. Vision Res. 1972 Nov;12(11):1841–1848. doi: 10.1016/0042-6989(72)90074-0. [DOI] [PubMed] [Google Scholar]
- Nachmias V. T. Further electron microscope studies on fibrillar organization of the ground cytoplasm of Chaos chaos. J Cell Biol. 1968 Jul;38(1):40–50. doi: 10.1083/jcb.38.1.40. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollack R., Osborn M., Weber K. Patterns of organization of actin and myosin in normal and transformed cultured cells. Proc Natl Acad Sci U S A. 1975 Mar;72(3):994–998. doi: 10.1073/pnas.72.3.994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollard T. D., Ito S. Cytoplasmic filaments of Amoeba proteus. I. The role of filaments in consistency changes and movement. J Cell Biol. 1970 Aug;46(2):267–289. doi: 10.1083/jcb.46.2.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollard T. D., Weihing R. R. Actin and myosin and cell movement. CRC Crit Rev Biochem. 1974 Jan;2(1):1–65. doi: 10.3109/10409237409105443. [DOI] [PubMed] [Google Scholar]
- Spooner B. S., Wessells N. K. Effects of cytochalasin B upon microfilaments involved in morphogenesis of salivary epithelium. Proc Natl Acad Sci U S A. 1970 Jun;66(2):360–361. doi: 10.1073/pnas.66.2.360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weber A., Murray J. M. Molecular control mechanisms in muscle contraction. Physiol Rev. 1973 Jul;53(3):612–673. doi: 10.1152/physrev.1973.53.3.612. [DOI] [PubMed] [Google Scholar]
- Weber K., Groeschel-Stewart U. Antibody to myosin: the specific visualization of myosin-containing filaments in nonmuscle cells. Proc Natl Acad Sci U S A. 1974 Nov;71(11):4561–4564. doi: 10.1073/pnas.71.11.4561. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wrenn J. T., Wessells N. K. Cytochalasin B: effects upon microfilaments involved in morphogenesis of estrogen-induced glands of oviduct. Proc Natl Acad Sci U S A. 1970 Jul;66(3):904–908. doi: 10.1073/pnas.66.3.904. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]