Retinal pigment epithelial integrity is compromised in the developing albino mouse retina. Issue 18 (19th May 2016)
- Record Type:
- Journal Article
- Title:
- Retinal pigment epithelial integrity is compromised in the developing albino mouse retina. Issue 18 (19th May 2016)
- Main Title:
- Retinal pigment epithelial integrity is compromised in the developing albino mouse retina
- Authors:
- Iwai‐Takekoshi, Lena
Ramos, Anna
Schaler, Ari
Weinreb, Samuel
Blazeski, Richard
Mason, Carol - Abstract:
- ABSTRACT: In the developing murine eye, melanin synthesis in the retinal pigment epithelium (RPE) coincides with neurogenesis of retinal ganglion cells (RGCs). Disruption of pigmentation in the albino RPE is associated with delayed neurogenesis in the ventrotemporal retina, the source of ipsilateral RGCs, and a reduced ipsilateral RGC projection. To begin to unravel how melanogenesis and the RPE regulate RGC neurogenesis and cell subpopulation specification, we compared the features of albino and pigmented mouse RPE cells during the period of RGC neurogenesis (embryonic day, E, 12.5 to 18.5) when the RPE is closely apposed to developing RGC precursors. At E12.5 and E15.5, although albino and pigmented RPE cells express RPE markers Otx2 and Mitf similarly, albino RPE cells are irregularly shaped and have fewer melanosomes compared with pigmented RPE cells. The adherens junction protein P‐cadherin appears loosely distributed within the albino RPE cells rather than tightly localized on the cell membrane, as in pigmented RPE. Connexin 43 (gap junction protein) is expressed in pigmented and albino RPE cells at E13.5 but at E15.5 albino RPE cells have fewer small connexin 43 puncta, and a larger fraction of phosphorylated connexin 43 at serine 368. These results suggest that the lack of pigment in the RPE results in impaired RPE cell integrity and communication via gap junctions between RPE and neural retina during RGC neurogenesis. Our findings should pave the way for furtherABSTRACT: In the developing murine eye, melanin synthesis in the retinal pigment epithelium (RPE) coincides with neurogenesis of retinal ganglion cells (RGCs). Disruption of pigmentation in the albino RPE is associated with delayed neurogenesis in the ventrotemporal retina, the source of ipsilateral RGCs, and a reduced ipsilateral RGC projection. To begin to unravel how melanogenesis and the RPE regulate RGC neurogenesis and cell subpopulation specification, we compared the features of albino and pigmented mouse RPE cells during the period of RGC neurogenesis (embryonic day, E, 12.5 to 18.5) when the RPE is closely apposed to developing RGC precursors. At E12.5 and E15.5, although albino and pigmented RPE cells express RPE markers Otx2 and Mitf similarly, albino RPE cells are irregularly shaped and have fewer melanosomes compared with pigmented RPE cells. The adherens junction protein P‐cadherin appears loosely distributed within the albino RPE cells rather than tightly localized on the cell membrane, as in pigmented RPE. Connexin 43 (gap junction protein) is expressed in pigmented and albino RPE cells at E13.5 but at E15.5 albino RPE cells have fewer small connexin 43 puncta, and a larger fraction of phosphorylated connexin 43 at serine 368. These results suggest that the lack of pigment in the RPE results in impaired RPE cell integrity and communication via gap junctions between RPE and neural retina during RGC neurogenesis. Our findings should pave the way for further investigation of the role of RPE in regulating RGC development toward achieving proper RGC axon decussation. J. Comp. Neurol. 524:3696–3716, 2016. © 2016 Wiley Periodicals, Inc. Abstract : In albinism, ipsilateral retinal ganglion cells (RGCs) are reduced. To dissect how melanin affects visual pathway development, we compared embryonic albino and pigmented retinal pigment epithelium (RPE). The perturbations of albino RPE cells charted here could affect RPE integrity and communication with neural precursors during RGC differentiation. … (more)
- Is Part Of:
- Journal of comparative neurology. Volume 524:Issue 18(2016)
- Journal:
- Journal of comparative neurology
- Issue:
- Volume 524:Issue 18(2016)
- Issue Display:
- Volume 524, Issue 18 (2016)
- Year:
- 2016
- Volume:
- 524
- Issue:
- 18
- Issue Sort Value:
- 2016-0524-0018-0000
- Page Start:
- 3696
- Page End:
- 3716
- Publication Date:
- 2016-05-19
- Subjects:
- melanosomes -- gap junctions -- connexin 43 -- P‐cadherin -- Zic2 -- retinal ganglion cells -- RRID: AB_638639 -- RRID: AB_476857 -- RRID: AB_86574 -- RRID: AB_2315623
Comparative neurobiology -- Periodicals
Neurology -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-9861 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cne.24025 ↗
- Languages:
- English
- ISSNs:
- 0021-9967
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4962.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11128.xml