A Method to Enhance Cell Survival on Bruch's Membrane in Eyes Affected by Age and Age-Related Macular Degeneration

被引:24
作者
Sugino, Ilene K. [1 ]
Rapista, Aprille [1 ]
Sun, Qian [1 ]
Wang, Jianqiu [1 ]
Nunes, Celia F. [1 ]
Cheewatrakoolpong, Noounanong [1 ]
Zarbin, Marco A. [1 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Inst Ophthalmol & Visual Sci, Newark, NJ 07101 USA
关键词
RETINAL-PIGMENT EPITHELIUM; EXTRACELLULAR-MATRIX MOLECULES; IN-VITRO; RPE TRANSPLANTATION; VISUAL FUNCTION; RCS RATS; PRESERVATION; RANIBIZUMAB; ATTACHMENT; BEHAVIOR;
D O I
10.1167/iovs.11-8400
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. To determine whether conditioned medium (CM) derived from bovine corneal endothelial cells (BCECs) can support transplanted cells on aged and age-related macular degeneration (AMD) Bruch's membrane (BM). METHODS. Retinal pigment epithelium (RPE) cells derived from human embryonic stem cells (hES-RPE) and cultured fetal and aged adult RPE were seeded onto the inner collagenous layer of submacular BM-choroid-sclera explants generated from aged and AMD human donor eyes. Paired explants were cultured in BCEC-CM or CM vehicle. To assess cell behavior after attachment to BM was established, explants were harvested after 21 days in culture. To assess whether sustained exposure to BCEC-CM was necessary for improved cell survival on BM, short exposure to BCEC-CM (3, 7, 14 days) was compared with 21-day exposure. Explants were harvested and evaluated by scanning electron and light microscopy. Extracellular matrix (ECM) deposition after exposure to BCEC-CM was evaluated following RPE cell removal after day 21 on tissue culture dishes or on BM. RESULTS. BCEC-CM significantly enhanced hES-RPE, fetal RPE, and aged adult RPE survival on BM, regardless of submacular pathology. Although shorter BCEC-CM exposure times showed significant improvement in cell survival compared with culture in CM vehicle, longer BCEC-CM exposure times were more effective. BCEC-CM increased RPE ECM deposition on tissue culture plastic and on BM. CONCLUSIONS. The results of this study indicate that RPE survival is possible on AMD BM and offer a method that could be developed for enhancing transplanted cell survival on AMD BM. Increased ECM deposition may account for improved cell survival after culture in BCEC-CM. (Invest Ophthalmol Vis Sci. 2011; 52:9598-9609) DOI: 10.1167/iovs.11-8400
引用
收藏
页码:9598 / 9609
页数:12
相关论文
共 39 条
[31]   Early attachment of uncultured retinal pigment epithelium from aged donors onto Bruch's membrane explants [J].
Tsukahara, I ;
Ninomiya, S ;
Castellarin, A ;
Yagi, F ;
Sugino, IK ;
Zarbin, MA .
EXPERIMENTAL EYE RESEARCH, 2002, 74 (02) :255-266
[32]   CYTOSKELETON, ADHESION, AND EXTRACELLULAR-MATRIX OF FETAL HUMAN RETINAL PIGMENTED EPITHELIAL-CELLS IN CULTURE [J].
TURKSEN, K ;
OPAS, M ;
KALNINS, VI .
OPHTHALMIC RESEARCH, 1989, 21 (01) :56-66
[33]   THE EFFECT OF EXTRACELLULAR-MATRIX MOLECULES ON THE INVITRO BEHAVIOR OF BOVINE ENDOTHELIAL-CELLS [J].
UNDERWOOD, PA ;
BENNETT, FA .
EXPERIMENTAL CELL RESEARCH, 1993, 205 (02) :311-319
[34]   Migration and proliferation of retinal pigment epithelium on extracellular matrix ligands [J].
Wang, Hao ;
Van Patten, Yancy ;
Sugino, Ilene K. ;
Zarbin, Marco A. .
JOURNAL OF REHABILITATION RESEARCH AND DEVELOPMENT, 2006, 43 (06) :713-722
[35]   Morphological and functional rescue in RCS rats after RPE cell line transplantation at a later stage of degeneration [J].
Wang, Shaomei ;
Lu, Bin ;
Girman, Sergej ;
Holmes, Toby ;
Bischoff, Nicolas ;
Lund, Raymond D. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2008, 49 (01) :416-421
[36]   Current concepts in the pathogenesis of age-related macular degeneration [J].
Zarbin, MA .
ARCHIVES OF OPHTHALMOLOGY, 2004, 122 (04) :598-614
[37]  
Zarbin MA, WIRES NANOM IN PRESS
[38]  
Zarbin Marco A, 2003, Trans Am Ophthalmol Soc, V101, P499
[39]   PATHWAY-BASED THERAPIES FOR AGE-RELATED MACULAR DEGENERATION An Integrated Survey of Emerging Treatment Alternatives [J].
Zarbin, Marco A. ;
Rosenfeld, Philip J. .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2010, 30 (09) :1350-1367