Spaceflight Effects and Molecular Responses in the Mouse Eye: Preliminary Observations After Shuttle Mission STS-133

Author:

Zanello Susana B.1,Theriot Corey A.2,Ponce Claudia Maria Prospero3,Chevez-Barrios Patricia34

Affiliation:

1. 1 Division of Space Life Sciences , Universities Space Research Association , Houston, TX United States ;

2. 2 Wyle Science, Technology and Engineering , Houston, TX , Department of Preventive Medicine and Community Health , University of Texas Medical Branch , Galveston, TX United States ;

3. 3 Pathology and Laboratory Medicine and Ophthalmology , Weill Medical College of Cornell University, The Methodist Hospital , Houston, TX United States ;

4. 4 Department of Pathology and Genomic Medicine, The Methodist Hospital , Houston, TX United States

Abstract

ABSTRACT Spaceflight exploration presents environmental stressors including microgravity-induced cephalad fluid shift and radiation exposure. Ocular changes leading to visual impairment in astronauts are of occupational health relevance. The effect of this complex environment on ocular morphology and function is poorly understood. Female 10-12 week-old BALB/cJ mice were assigned to a flight (FLT) group flown on shuttle mission STS-133, Animal Enclosure Module ground control group (AEM), or vivarium-housed (VIV) ground controls. Eyes were collected at 1, 5, and 7 days after landing and were fixed for histological sectioning. The contralateral eye was used for gene expression profiling by RT-qPCR. Sections were visualized by hematoxylin/eosin stain and processed for 8-hydroxy-2’-deoxyguanosine (8-OHdG), caspase-3, and glial fibrillary acidic protein (GFAP) and β-amyloid double-staining. 8-OHdG and caspase-3 immunoreactivity was increased in the retina in FLT samples at return from flight (R+1) compared to ground controls, and decreased at day 7 (R+7). β-amyloid was seen in the nerve fibers at the post-laminar region of the optic nerve in the flight samples (R+7). Expression of oxidative and cellular stress response genes was upregulated in the retina of FLT samples upon landing, followed by lower levels by R+7. These results suggest that reversible molecular damage occurs in the retina of mice exposed to spaceflight and that protective cellular pathways are induced in the retina and optic nerve in response to these changes.

Publisher

Walter de Gruyter GmbH

Reference54 articles.

1. Abramoff, M.D., Magalhaes, P.J., and Ram, S.J. 2004. Image processing with ImageJ. Biophotonics International. 11: 36-42.

2. Awasthi, N. and Wagner, B.J. 2005. Upregulation of heat shock protein expression by proteasome inhibition: an antiapoptotic mechanism in the lens. Investigative Ophthalmology & Visual Science. 46: 2082-2091.

3. Byun, J., Verardo, M.R., Sumengen, B., Lewis, G.P., Manjunath, B.S., and Fisher, S.K. 2006. Automated tool for the detection of cell nuclei in digital microscopic images: application to retinal images. Molecular Vision. 12: 949-960.

4. Chen, D., Pacal, M., Wenzel, P., Knoepfler, P.S., Leone, G., and Bremner, R. 2009. Division and apoptosis of E2f-deficient retinal progenitors. Nature. 462: 925-929.

5. Cucinotta, F.A., Manuel, F.K., Jones, J., Iszard, G., Murrey, J., Djojonegro, B., and Wear, M. 2001. Space radiation and cataracts in astronauts. Radiation Research. 156: 460-466.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3