PAX6 (+5a) Expression in Adipose Tissue-Derived Stem Cells Induces Retinal Ganglion Cells

Habib Rezanejadbardeji, F. Haddad, Z. Soheili, M. Matin, S. Samiei, S. Z. Vahed
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Abstract

Glaucoma remains one of the major causes of blindness in today's world. The progressive field of stem cell proposes an exciting potential for discovering novel therapies. Here, we report the development of an easy and high throughput method for differentiation of retinal ganglion cells (RGC) and bipolar cells from human adipose tissue-derived mesenchymal stem cells (hADSCs) using PAX6 (+5a) gene expression, a master gene in development of the vertebrate visual system. HADSCs was isolated from fat tissues and confirmed by their surface markers and differentiation potential into adipocytes and osteocytes lineages. Then, the coding region of human PAX6 (+5a) gene was cloned and lentiviral particles were produced. HADSCs differentiation was characterized by morphological characteristics, qRT-PCR and immunocytochemistry (ICC). The hADSCs were isolated successfully with high yield and purity (99%). After 30 hours post transduction by pLEX-pax6- pur lentiviral vectors in fibronectin supplemented medium, cells gradually showed the characteristic morphology of neuronal cells. QRT- PCR and ICC confirmed deriving of mainly RGC and marginally bipolar cells. The current investigation demonstrates the feasibility of differentiation of RGCs and bipolar cells from hADSCs using expression of PAX6 (+5a) in the medium supplemented by fibronectin.
PAX6 (+5a)在脂肪组织源性干细胞中的表达诱导视网膜神经节细胞
青光眼仍然是当今世界致盲的主要原因之一。干细胞领域的进步为发现新的治疗方法提供了令人兴奋的潜力。在这里,我们报道了一种简单、高通量的方法,利用脊椎动物视觉系统发育的主要基因PAX6 (+5a)基因表达,从人脂肪组织来源的间充质干细胞(hADSCs)分化视网膜神经节细胞(RGC)和双极细胞。从脂肪组织中分离出hascs,并通过其表面标记物和向脂肪细胞和骨细胞谱系的分化潜力进行了证实。然后克隆人PAX6 (+5a)基因编码区,制备慢病毒颗粒。采用形态学、qRT-PCR和免疫细胞化学(ICC)对hscs的分化进行表征。成功地分离出了高产量、高纯度(99%)的hscs。pLEX-pax6- pur慢病毒载体在添加纤维连接蛋白的培养基中转导30小时后,细胞逐渐表现出神经元细胞的特征形态。QRT- PCR和ICC证实主要为RGC细胞和边缘双极性细胞。目前的研究表明,在添加纤维连接蛋白的培养基中表达PAX6 (+5a),可以从hADSCs分化为RGCs和双极细胞。
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