Thyroid-beta2 and the retinoid RAR-alpha, RXR-gamma and ROR-beta2 receptor mRNAs; expression profiles in mouse retina, retinal explants and neocortex.
Författare
Summary, in English
In neonatal retinal explants cultured long-term green cones are missing. Recently it was reported that thyroid hormone beta2 receptors (TR-beta2) are essential for these green cones to differentiate. Therefore transcript level of these receptors was investigated in our mouse retinal explants. However, thyroid receptors function as heterodimers with retinoid receptors (RR); so the fate of selected RRs was similarly analyzed using semi-quantitative RT-PCR. Loss of TR-beta2 and RR (RXR-gamma and ROR-beta2) mRNAs was observed after culturing the neonatal retina for 12 days. This indicates that these proteins are involved in determination of green cone identity. In addition, levels of the selected RR transcripts are differentially affected by short- or long-term culture. In the latter case an attached retinal pigment epithelium seems to play a protective role. Furthermore, divergent diurnal peaks of RR mRNAs are present in young as well as aged mouse retina and neocortex. This data might be relevant in the context of human ageing disorders.
Publiceringsår
2002
Språk
Engelska
Sidor
745-750
Publikation/Tidskrift/Serie
NeuroReport
Volym
13
Issue
6
Länkar
Dokumenttyp
Artikel i tidskrift
Förlag
Lippincott Williams & Wilkins
Ämne
- Neurosciences
Nyckelord
- Mice
- Inbred C3H
- Neocortex : cytology
- Neocortex : growth & development
- Neocortex : metabolism
- Organ Culture : methods
- RNA
- Messenger : metabolism
- Receptors
- Cell Surface : genetics
- Retinoic Acid : genetics
- Thyroid Hormone : genetics
- Retina : cytology
- Retina : metabolism
- Retina : growth & development
- Support
- Non-U.S. Gov't
- Transcription Factors : genetics
- Transcription
- Genetic : physiology
- Up-Regulation : genetics
- Male
- Gene Expression Regulation : physiology
- Female
- Down-Regulation : genetics
- Dark Adaptation : genetics
- Circadian Rhythm : genetics
- Cell Differentiation : genetics
- Animal
- Aging : metabolism
Status
Published
ISBN/ISSN/Övrigt
- ISSN: 1473-558X