Modulation of the rate of retinal degeneration in T17M RHO mice by reprogramming the unfolded protein response.

Abstract

The goal of this study is to validate whether reprogramming of the UPR via modulation of pro-apoptotic caspase-7 and CHOP proteins could be an effective approach to slow down the rate of retinal degeneration in ADRP mice. In order to pursue our goal we created the T17M RHO CASP7 and T17M RHO CHOP mice to study the impact of the CASP7 or CHOP ablations in T17M RHO retina by ERG, SD-OCT, histology and western blot analysis. The scotopic ERG demonstrated that the ablation of the CASP7 in T17M RHO retina leads to significant preservation of the function of photoreceptors compared to control. Surprisingly, the ablation of pro-apoptotic CHOP protein in T17M RHO mice led to a more severe form of retinal degeneration. Results of the SD-OCT and histology were in agreement with the ERG data. The further analysis demonstrated that the preservation of the structure and function or the acceleration of the onset of the T17M RHO photoreceptor degeneration occurred via reprogramming of the UPR. In addition, the CASP7 ablation leads to the inhibition of cJUN mediated apoptosis, while the ablation of CHOP induces an increase in the HDAC. Thus, manipulation with the UPR requires careful examination in order to achieve a therapeutic effect.

• Authors: Shreyasi Choudhury, Sonali Nashine, Yogesh Bhootada, Mansi Motiwale Kunte, Oleg Gorbatyuk, Alfred S Lewin, Marina Gorbatyuk
• Journal: Advances in experimental medicine and biology (Adv Exp Med Biol) Vol. 801 Pg. 455-62 ( 2014) ISSN: 0065-2598 [Print] United States
• PMID: 24664731 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Ddit3 protein, mouse
• Transcription Factor CHOP
• Rhodopsin
• Casp7 protein, mouse
• Caspase 7

Topics

• Animals
• Apoptosis (genetics)
• Caspase 7 (genetics, metabolism)
• Disease Models, Animal
• Electroretinography
• Female
• Male
• Mice
• Mice, Inbred C57BL
• Mice, Knockout
• Retinal Degeneration (genetics, metabolism, pathology)
• Retinitis Pigmentosa (genetics, metabolism, pathology)
• Rhodopsin (genetics, metabolism)
• Transcription Factor CHOP (genetics, metabolism)
• Unfolded Protein Response (genetics)