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Corneal epithelial cells and corneal stent as well as preparation method and application thereof

A corneal epithelial cell and cornea technology, applied in epidermal cells/skin cells, embryonic cells, animal cells, etc., can solve the problems of corneal shortage, immune rejection, obstacles, etc., achieve continuous cell transparency, reduce immune rejection obstacles, low immunity original effect

Active Publication Date: 2021-04-13
UNIVERSITY OF MACAU
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although allogeneic keratoplasty is one of the main treatment options, the shortage of donated corneas and the potential for immune rejection remain major obstacles

Method used

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  • Corneal epithelial cells and corneal stent as well as preparation method and application thereof
  • Corneal epithelial cells and corneal stent as well as preparation method and application thereof
  • Corneal epithelial cells and corneal stent as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] hESCs were induced to differentiate into CECs in defined albumin-free E6 medium

[0046] H9hESCs routinely cultured in E8 were differentiated into CECs in E6 according to the flow chart (Fig. 1A). By day 15 of differentiation, the cells mostly developed an epithelial morphology, some of which had a polygonal morphology typical of CECs (Fig. 1B). In this example, the cells were subcultured on day 40, and the cells were immunostained within one week after subculture. Most cells were positive for the CEC progenitor markers TP63 and PAX6, another CEC progenitor keratin-19 (KRT19), and the basal CEC marker KRT15. After 20 days of culture in E6 medium, many cells were also positive for two terminally differentiated CEC markers, KRT3 and KRT12 (Fig. 1C).

[0047] Gene expression was analyzed by RT-qPCR, and differentiated hESCs were collected every two weeks to study the expression of lineage-specific marker genes. The expression of the pluripotency marker OCT4 was downregu...

Embodiment 2

[0050] Gene expression profiles of hESCs differentiated into CECs

[0051] As expected, expression of pluripotency genes was significantly reduced at week 2 of differentiation and remained low. In this example, the expression of surface ectoderm markers was detected to increase at the 2nd week and the 4th week, and the expression of LSC and embryonic CEC markers were detected at the 6th and 8th weeks. Meanwhile, expression of neural and retinal markers increased at week 2, peaked at week 4, and then gradually decreased, whereas expression of lens progenitor cell markers continued to increase during all 8 weeks of differentiation. However, expression of adult CEC markers remained low in differentiated cells. These data demonstrate that the expression of eye development genes, particularly those associated with epidermal ectoderm and embryonic CEC, is induced in E6 differentiated cells and that the multistep differentiation process somehow recapitulates the embryonic process of...

Embodiment 3

[0053] Proliferation capacity of hESC-derived CECs

[0054] LSCs first differentiate into CEC progenitors, migrate to the basal layer of the cornea, and terminally differentiate into CECs during corneal regeneration and homeostasis [42] . One of the characteristics of CEC progenitor cells is their ability to proliferate rapidly. Therefore, this example analyzes whether hESC-derived CECs are proliferative. First, in this example, the proliferative ability of CECs differentiated from H9 and CT3 hESCs was monitored respectively. Although neither CEC line proliferated as rapidly as the parental hESCs, CECs still proliferated at a relatively high rate throughout the 3-day observation period (Fig. 3A). Second, cell cycle assays showed that approximately 40% of CECs were in S and G2 / M phases ( Figure 3-B1~Figure 3-B3 ). Third, nearly half of the CECs from H9 or CT3 were KRT15 + Cells are Ki67 + (Fig. 3C and 3D). All these data indicate the proliferative nature of the cells. ...

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Abstract

The invention discloses corneal epithelial cells, corneal scaffolds and their preparation methods and applications, and relates to the field of corneal disease drugs. The preparation method of corneal epithelial cells disclosed in the present invention is to inoculate human embryonic stem cells into E6 medium for culturing, so that human embryonic stem cells can differentiate into corneal epithelial cells, and the preparation method can continuously provide corneal epithelial cells with rapid proliferation ability The cells can be used to prepare corneal stents, or to prepare medicines for treating corneal diseases.

Description

technical field [0001] The invention relates to the field of corneal disease drugs, in particular to a corneal epithelial cell, a corneal stent and a preparation method and application thereof. Background technique [0002] Corneal disease affects millions of people around the world. For example, limbal stem cell deficiency (LSCD) is characterized by the loss of limbal stem cells, which are critical for corneal epithelial cell (CEC) regeneration. Limbal stem cells (LSCs) differentiate into CECs through intermediate progenitors [1] . Therefore, loss or insufficiency of LSC will lead to keratoconjunctivalization, chronic inflammation and potential vision loss after corneal injury [2] . Although restoring the limbal microenvironment has a certain effect on the early treatment of LSCD [3] , but corneal and LSC transplantation are by far the most effective [4] . However, autologous LSC transplantation has the potential to damage the healthy cornea of ​​the contralateral do...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N5/071C12N5/079A61L27/38A61P27/02
CPCA61K35/36A61L27/3813A61L27/3895A61L2430/16A61L2430/40A61P27/02C12N5/0621C12N5/0625C12N2506/02
Inventor 徐仁和杨娟郑德锦朴政友
Owner UNIVERSITY OF MACAU
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