March 1999
Volume 40, Issue 3
Free
Articles  |   March 1999
Expression patterns of neurturin and its receptor components in developing and degenerative mouse retina.
Author Affiliations
  • C Jomary
    Department of Pharmacology, The Rayne Institute, United Medical and Dental Schools of Guy's and St. Thomas' Hospitals, London, United Kingdom.
  • M Thomas
    Department of Pharmacology, The Rayne Institute, United Medical and Dental Schools of Guy's and St. Thomas' Hospitals, London, United Kingdom.
  • J Grist
    Department of Pharmacology, The Rayne Institute, United Medical and Dental Schools of Guy's and St. Thomas' Hospitals, London, United Kingdom.
  • J Milbrandt
    Department of Pharmacology, The Rayne Institute, United Medical and Dental Schools of Guy's and St. Thomas' Hospitals, London, United Kingdom.
  • M J Neal
    Department of Pharmacology, The Rayne Institute, United Medical and Dental Schools of Guy's and St. Thomas' Hospitals, London, United Kingdom.
  • S E Jones
    Department of Pharmacology, The Rayne Institute, United Medical and Dental Schools of Guy's and St. Thomas' Hospitals, London, United Kingdom.
Investigative Ophthalmology & Visual Science March 1999, Vol.40, 568-574. doi:
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      C Jomary, M Thomas, J Grist, J Milbrandt, M J Neal, S E Jones; Expression patterns of neurturin and its receptor components in developing and degenerative mouse retina.. Invest. Ophthalmol. Vis. Sci. 1999;40(3):568-574.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: Neurturin (NTN) and its receptor components (GFRalpha2 and Ret) play an important role in the survival of different populations of neurons in the central and peripheral nervous systems. To gain insight into their possible functions throughout normal retinal development and during retinal neuronal apoptosis, the retinal distribution of expression of NTN and GFRalpha2 mRNAs and Ret protein were compared in control and retinal degeneration (rd) mice. METHODS: Eyes from control and rd animals were fixed in paraformaldehyde before sectioning. For in situ hybridization, retinal sections were hybridized with 35S-radiolabeled sense and antisense riboprobes for murine NTN and GFRalpha2 and were autoradiographed. Ret localization was detected by immunofluorescence. RESULTS: Neurturin mRNA expression was modulated through normal postnatal retinal development and was localized primarily to the inner retina and photoreceptor outer segments. GFRalpha2 mRNA displayed a diffuse developmental pattern of expression, but in the mature normal retina, NTN and GFRalpha2 mRNAs were more closely colocalized. Ret protein was localized particularly at the outer segments of photoreceptors, inner retina, and ganglion cell layers, but there were no prominent differences among genotypes. Increased NTN mRNA expression was detected in the retinal pigment epithelium and neural retina in concert with photoreceptor degeneration in rd mouse. In contrast, the level of GFRalpha2 mRNA was lower in rd compared with that in normal retina. CONCLUSIONS: These results suggest that NTN and its receptor are involved in retinal postnatal development and maintenance and that alterations in their transcription patterns are associated with inherited retinal degeneration.

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