Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Cell loaded 3D bioprinted GelMA hydrogels for corneal stroma engineering
Date
2020-01-01
Author
BEKTAŞ, CEMİLE
Hasırcı, Vasıf Nejat
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
170
views
0
downloads
Cite This
Tissue engineering aims to replace missing or damaged tissues and restore their functions. Three-dimensional (3D) printing has been gaining more attention because it enables the researchers to design and produce cell loaded constructs with predetermined shapes, sizes, and interior architecture. In the present study, a 3D bioprinted corneal stroma equivalent was designed to substitute for the native tissue. Reproducible outer and inner organization of the stroma was obtained by optimizing printing conditions such as the nozzle speed in the x-y direction and the spindle speed. 3D printed GelMA hydrogels were highly stable in PBS during three weeks of incubation (8% weight loss). Live-Dead cell viability assay showed 98% cell viability on day 21 indicating that printing conditions were suitable for keratocyte printing. Mechanical properties of the cell loaded 3D printed hydrogels increased 2-fold during this incubation period and approached those of the native cornea (ca. 20 kPa vs. 27 kPa, respectively). Expression of collagens types I and V, and proteoglycan (decorin) in keratocytes indicates maintenance of the phenotype in the hydrogels. Transparency of cell-loaded and cell-free hydrogels was over 80% (at 700 nm) during the three week culture period and comparable to that of the native cornea (85%) at the same wavelength. Thus, GelMA hydrogels bioprinted with keratocytes mimic the biological and physical properties of the corneal stroma with their excellent transparency, adequate mechanical strength, and high cell viability.
Subject Keywords
Pigment epithelial-cells
,
Mechanical-properties
,
Equivalents
,
Induction
,
Membranes
,
Eye
,
Scaffold
,
Keratocytes
URI
https://hdl.handle.net/11511/31230
Journal
BIOMATERIALS SCIENCE
DOI
https://doi.org/10.1039/c9bm01236b
Collections
Graduate School of Natural and Applied Sciences, Article
Suggestions
OpenMETU
Core
3D printed, cell carrying GelMA hydrogels in corneal stroma engineering
Bektaş, Cemile; Hasırcı, Vasıf Nejat; Altan Sakarya, Ayşe Burcu; Department of Biotechnology (2018)
Tissue engineering is an emerging field which aims to replace missing or damaged tissues and restore their functions. Three dimensional (3D) printing has recently been in the heart of tissue engineering which enables design and production cell loaded or cell carrying scaffolds with shapes, sizes, and porosities specific for the patients. Corneal damages and diseases are the third major cause for blindness after cataract and glaucoma. Transplantation and keratoprostheses are the only acceptable treatments fo...
Advanced cell therapies with and without scaffolds
Demirbag, Birsen; HURİ, PINAR; KÖSE, GAMZE; Buyuksungur, Arda; Hasırcı, Vasıf Nejat (2011-12-01)
Tissue engineering and regenerative medicine aim to produce tissue substitutes to restore lost functions of tissues and organs. This includes cell therapies, induction of tissue/organ regeneration by biologically active molecules, or transplantation of in vitro grown tissues. This review article discusses advanced cell therapies that make use of scaffolds and scaffold-free approaches. The first part of this article covers the basic characteristics of scaffolds, including characteristics of scaffold material...
Wet spun PCL scaffolds for tissue engineering
Malikmammadov, Elbay; Hasırcı, Nesrin; Endoğan Tanır, Tuğba; Department of Micro and Nanotechnology (2017)
Scaffolds produced for tissue engineering applications are promising alternatives to be used in healing and regeneration of injured tissues and organs. In this study, fibrous poly(ε-caprolactone) (PCL) scaffolds were prepared by wet spinning technique and modified by addition of β-tricalcium phosphate (β-TCP) and by immobilizing gelatin onto fibers. Meanwhile, gelatin microspheres carrying Ceftriaxone sodium (CS), a model antibiotic, were added onto the scaffolds and antimicrobial activity of CS was investi...
Cellulose-based electrospun scaffolds for tissue engineering applications
Atila, Deniz Hazal; Tezcaner, Ayşen; Yazgan Karataş, Ayten; Department of Engineering Sciences (2014)
With the use of a scaffold as support material, adequate number of cells, and bioactive molecules, tissue engineering applications intend to promote the regeneration of tissues or to replace failing or malfunctioning tissues/organs. In this study, electrospun 2D and 3D cellulose-based scaffolds were aimed to be produced with pullulan (PULL). Cellulose acetate (CA) and PULL powders in various ratios (80/20, 50/50, and 80/20) were dissolved in DMAc/DMSO solvent system and electrospun as either 2D or 3D forms....
Tissue engineering of full-thickness human oral mucosa
Kınıkoğlu, Beste; Hasırcı, Vasıf Nejat; Damour, Odile; Department of Biotechnology (2010)
Tissue engineered human oral mucosa has the potential to fill tissue deficits caused by facial trauma or malignant lesion surgery. It can also help elucidate the biology of oral mucosa and serve as an alternative to in vivo testing of oral care products. The aim of this thesis was to construct a tissue engineered full-thickness human oral mucosa closely mimicking the native tissue. To this end, the feasibility of the concept was tested by co-culturing fibroblasts and epithelial cells isolated from normal hu...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
C. BEKTAŞ and V. N. Hasırcı, “Cell loaded 3D bioprinted GelMA hydrogels for corneal stroma engineering,”
BIOMATERIALS SCIENCE
, pp. 438–449, 2020, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/31230.