Disruption of microfilament organization and deregulation of disk membrane morphogenesis by cytochalasin D in rod and cone photoreceptors
- PMID: 3397406
- DOI: 10.1002/cne.902720202
Disruption of microfilament organization and deregulation of disk membrane morphogenesis by cytochalasin D in rod and cone photoreceptors
Abstract
Morphogenesis of photoreceptor outer segment disks appears to occur by an evagination of the ciliary plasma membrane (Steinberg et al., J Comp Neurol 190:501-519, '80). We tested if polymerized actin (F-actin) was necessary for the regulation of this postulated process by incubating Xenopus eyecups with 5 or 25 microM cytochalasin D for 6-28 hours. During the second hour, the incubation medium contained 3H-leucine. Both concentrations of cytochalasin resulted in: 1) dissolution of the rhodamine-phalloidin labeling pattern of photoreceptors, and 2) collapse of the calycal processes (which are normally filled with actin filaments) and disappearance of the inner segment microfilaments. In addition, the few most basal rod and cone outer segment disks appeared several times their normal diameter. These oversized disks had incorporated 3H-leucine and extended along the margin of the outer or inner segment. The nature of the overgrown disks is consistent only with a morphogenetic process involving evaginations of the ciliary plasma membrane. Deregulation by cytochalasin D was manifest by excessive growth of a few nascent disks rather than normal growth of many. Therefore, the normal network of actin filaments is apparently not necessary for continued evagination of the membrane, but it does seem to be an essential part of the mechanism that initiates the evagination of the ciliary plasma membrane and/or the mechanism that controls how far nascent disks grow.
Similar articles
-
Actin-dependent myoid elongation in teleost rod inner/outer segments occurs in the absence of net actin polymerization.Cell Motil Cytoskeleton. 1992;21(3):235-51. doi: 10.1002/cm.970210307. Cell Motil Cytoskeleton. 1992. PMID: 1581976
-
Cytochalasin D disrupts outer segment disc morphogenesis in situ in rabbit retina.Invest Ophthalmol Vis Sci. 1989 Feb;30(2):339-42. Invest Ophthalmol Vis Sci. 1989. PMID: 2914762
-
The actin network in the ciliary stalk of photoreceptors functions in the generation of new outer segment discs.J Comp Neurol. 1996 Dec 2;376(1):128-42. doi: 10.1002/(SICI)1096-9861(19961202)376:1<128::AID-CNE8>3.0.CO;2-5. J Comp Neurol. 1996. PMID: 8946288
-
Actin filaments and photoreceptor membrane turnover.Bioessays. 1991 Apr;13(4):171-8. doi: 10.1002/bies.950130405. Bioessays. 1991. PMID: 1859395 Review.
-
Membrane and microfilament organization and vasopressin action in transporting epithelia.Soc Gen Physiol Ser. 1987;42:259-75. Soc Gen Physiol Ser. 1987. PMID: 3333192 Review. No abstract available.
Cited by
-
Molecular basis for photoreceptor outer segment architecture.Prog Retin Eye Res. 2016 Nov;55:52-81. doi: 10.1016/j.preteyeres.2016.05.003. Epub 2016 Jun 1. Prog Retin Eye Res. 2016. PMID: 27260426 Free PMC article. Review.
-
Submembrane assembly and renewal of rod photoreceptor cGMP-gated channel: insight into the actin-dependent process of outer segment morphogenesis.J Neurosci. 2014 Jun 11;34(24):8164-74. doi: 10.1523/JNEUROSCI.1282-14.2014. J Neurosci. 2014. PMID: 24920621 Free PMC article.
-
The Formation and Renewal of Photoreceptor Outer Segments.Cells. 2024 Aug 15;13(16):1357. doi: 10.3390/cells13161357. Cells. 2024. PMID: 39195247 Free PMC article. Review.
-
Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.Nat Commun. 2017 Aug 16;8(1):271. doi: 10.1038/s41467-017-00111-8. Nat Commun. 2017. PMID: 28814713 Free PMC article.
-
Morphogenesis of the photoreceptor outer segment during postnatal development in the mouse (BALB/c) retina.Cell Tissue Res. 1992 Jul;269(1):39-48. doi: 10.1007/BF00384724. Cell Tissue Res. 1992. PMID: 1423483
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous