Protective Role of Decellularized Human Amniotic Membrane from Oxidative Stress-Induced Damage on Retinal Pigment Epithelial Cells

被引:10
作者
Krishna, Lekshmi [1 ,2 ]
Dhamodaran, Kamesh [1 ,7 ]
Subramani, Murali [1 ]
Ponnulagu, Murugeswari [1 ]
Jeyabalan, Nallathambi [3 ]
Meka, Sai Rama Krishna [4 ]
Jayadev, Chaitra [5 ]
Shetty, Rohit [6 ]
Chatterjee, Kaushik [4 ]
Khora, Samanta Sekhar [2 ]
Das, Debashish [1 ]
机构
[1] Narayana Nethralaya Fdn, Stem Cell Res Lab, GROW Labs, 258-A Bommasandra Ind Area, Bangalore 258 A, Karnataka, India
[2] VIT Univ, Sch Biosci & Technol, Vellore, Tamil Nadu, India
[3] Narayana Nethralaya Fdn, Grow Labs, 258-A Bommasandra Ind Area, Bangalore 258 A, Karnataka, India
[4] Indian Inst Sci, Dept Mat Engn, Bangalore, Karnataka, India
[5] Narayana Nethralaya Eye Inst, Dept Vitreo Retinal Serv, 258-A Bommasandra Ind Area, Bangalore, Karnataka, India
[6] Narayana Nethralaya Eye Inst, Dept Cornea & Refract Surg, 258-A Bommasandra Ind Area, Bangalore, Karnataka, India
[7] Univ Houston, Ocular Surface Inst, Coll Optometry, Dept Basic Sci, Houston, TX 77204 USA
关键词
decellularized human amniotic membrane; retinal pigment epithelium; oxidative stress; RPE CELLS; GROWTH-FACTOR; MESENCHYMAL TRANSITION; POTENTIAL APPLICATIONS; MOLECULAR-MECHANISMS; SIGNALING PATHWAYS; PROTEIN EXPRESSION; RCS RATS; TRANSPLANTATION; ADHESION;
D O I
10.1021/acsbiomaterials.8b00769
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Oxidative stress is an important cause for several retinal aging diseases. Cell therapy using a decellularized human amniotic membrane (dHAM) as a tissue scaffold for retinal pigment epithelial cells has a potential therapeutic role under such pathological conditions. This is attributed by the anti-inflammatory, antimicrobial, low-immunogenicity aspects of dHAM, apart from harboring a drug reservoir potential. The underlying mechanisms for maintaining the physiological properties of transplanted cells and their survival in a diseased milieu using dHAM has remained unexplored/unanswered. Hence, we investigated the potential role of dHAM in preserving the cellular functions of retinal pigment epithelium in an oxidative stress environment. Adult human retinal pigment epithelial (ARPE-19) cells were cultured on dHAM or tissue culture dishes under hyperoxia. Gene expression, immunofluorescence staining, enzyme-linked immunosorbent assay (ELISA), and scanning electron microscopy (SEM) were performed to assess the levels of reactive oxygen species, proliferation, apoptosis, epithelial-mesenchymal transition, phagocytosis, and secretion of vascular endothelial factors. These results indicate reduced epithelial-mesenchymal transition, generation of reactive oxygen species (p <= 0.0001), and apoptosis (p <= 0.05) in cells cultured on dHAM, compared to those on tissue culture dishes under oxidative stress conditions. Concomitantly, the secretion of the vascular endothelial growth factor was significantly reduced (p <= 0.01) on dHAM. Phagocytic activity was significantly higher (p <= 0.001) in cells cultured on dHAM and were comparable to those cells cultured on tissue culture dishes. SEM images showed a clustered growth pattern on dHAM compared to an elongated morphology when cultured on tissue culture dishes under oxidative stress conditions. These findings demonstrate the utility of dHAM as a scaffold for growing retinal epithelial cells and to maintain their physiological properties in an oxidative stress condition with a potential to develop regenerative medicine strategies to treat degenerative eye diseases.
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收藏
页码:357 / 372
页数:31
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