Research Article
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Year 2018, , 145 - 151, 04.07.2018
https://doi.org/10.18621/eurj.342109

Abstract

References

  • [1] Matsusaki M, Case CP, Akashi M. Three-dimensional cell culture technique and pathophysiology. Adv Drug Deliv Rev 2014;74:95-103.
  • [2] Michelini E, Cevenini L, Mezzanotte L, Coppa A, Roda A. Cell-based assays: fuelling drug discovery. Anal Bioanal Chem 2010;398:227-38.
  • [3] Drewe J, Cai SX. Cell-based apoptosis assays in oncology drug discovery. Expert Opin Drug Discov 2010;5:583-96.
  • [4] Vogel V, Baneyx G. The tissue engineering puzzle: a molecular perspective. Annu Rev Biomed Eng 2003;5:441-63.
  • [5] Rosa V, Zhang Z, Grande R, Nör J. Dental pulp tissue engineering in full-length human root canals. J Dent Res 2013;92:970-5.
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  • [7] Kelm JM, Djonov V, Ittner LM, Fluri D, Born W, Hoerstrup SP, et al. Design of custom-shaped vascularized tissues using microtissue spheroids as minimal building units. Tissue Eng 2006;12:2151-60.
  • [8] Rouwkema J, Rivron NC, van Blitterswijk CA. Vascularization in tissue engineering. Trends Biotechnol 2008;26:434-41.
  • [9] Dissanayaka W, Zhu L, Hargreaves K, Jin L, Zhang C. Scaffold-free prevascularized microtissue spheroids for pulp regeneration. J Dent Res 2014;93:1296-303.
  • [10] Mendicino M, Bailey AM, Wonnacott K, Puri RK, Bauer SR. MSC-based product characterization for clinical trials: an FDA perspective. Cell Stem Cell 2014;14:141-5.
  • [11] Karnieli O, Friedner OM, Allickson JG, Zhang N, Jung S, Fiorentini D, et al. A consensus introduction to serum replacements and serum-free media for cellular therapies. Cytotherapy 2017;19:155-69.
  • [12] Yu M, Bardia A, Aceto N, Bersani F, Madden MW, Donaldson MC, et al. Cancer therapy. Ex vivo culture of circulating breast tumor cells for individualized testing of drug susceptibility. Science 2014;345:216-20.
  • [13] Kim CS, Mout R, Zhao Y, Yeh Y-C, Tang R, Jeong Y, et al. Co-delivery of protein and small molecule therapeutics using nanoparticle-stabilized nanocapsules. Bioconjug Chem 2015;26:950-4.
  • [14] Rouwkema J, Khademhosseini A. Vascularization and angiogenesis in tissue engineering: beyond creating static networks. Trends Biotechnol 2016;34:733-45.
  • [15] Karaman O, Onak G, Demirci EA, Kahraman E. Integrin binding peptide promotes in vitro wound closure in the L929 mouse fibroblasts. Eur Res J 2017;3:207-13.
  • [16] Gstraunthaler G, Lindl T, van der Valk J. A plea to reduce or replace fetal bovine serum in cell culture media. Cytotechnology 2013;65:791-3.
  • [17] Napolitano AP, Dean DM, Man AJ, Youssef J, Ho DN, Rago AP, et al. Scaffold-free three-dimensional cell culture utilizing micromolded nonadhesive hydrogels. Biotechniques 2007;43:494-500.
  • [18] Sanz-Nogués C, O’Brien T. In vitro models for assessing therapeutic angiogenesis. Drug Discov Today 2016;21:1495-503.

Determination of minimum serum concentration to develop scaffold free micro-tissue

Year 2018, , 145 - 151, 04.07.2018
https://doi.org/10.18621/eurj.342109

Abstract

Objective. Formation of three-dimensional (3D) micro-tissues
without scaffolds are widely used not only to define in vivo tissue formation mechanisms but also the development of
different tissue-specific drugs. However, depending on high serum and growth
factor concentrations, it would be hard to identify major effective biological
cues on micro-tissue formation. The aim of the study is to determine the effect
of different serum concentrations on Human Umbilicial Vein Endothelial Cells
(HUVECs) micro-tissue formation. Methods. Micro-tissue of HUVEC line
was formed by using 3D petri dish technique with medium containing 0%, 1%, 5%
and 10% fetal bovine serum (FBS). On the 7th day after micro-tissue
formation, live/dead cells analysis was conducted. Micrograph taken on days 1,
3, 5 and 7th of micro-tissue formation were determined by image
analysis with ImageJ. Results. Sizes of micro-tissue
formed with 0% FBS on day 1 and 3 determined as 277 ± 12 µm and 279 ± 20 µm,
respectively; however, especially on day 7 micro-tissue size significantly
decreased to 229 ± 6 µm. When live/dead analysis results were examined, high
cell viability was observed in 5% and 10% FBS concentration. Although
micro-tissue like structures were observed in 0% and 1% FBS concentrations dead
cell ratio considerably increased compared to 5% and 10% FBS concentration. Conclusions.
It has been determined that 0% and 1% serum are appropriate for determining
the efficacy of biomimetic peptides and different extracellular matrix proteins
on micro-tissue formation parameters of HUVEC. High cell viability in
micro-tissues was observed with 5% and 10% serum concentrations.


















References

  • [1] Matsusaki M, Case CP, Akashi M. Three-dimensional cell culture technique and pathophysiology. Adv Drug Deliv Rev 2014;74:95-103.
  • [2] Michelini E, Cevenini L, Mezzanotte L, Coppa A, Roda A. Cell-based assays: fuelling drug discovery. Anal Bioanal Chem 2010;398:227-38.
  • [3] Drewe J, Cai SX. Cell-based apoptosis assays in oncology drug discovery. Expert Opin Drug Discov 2010;5:583-96.
  • [4] Vogel V, Baneyx G. The tissue engineering puzzle: a molecular perspective. Annu Rev Biomed Eng 2003;5:441-63.
  • [5] Rosa V, Zhang Z, Grande R, Nör J. Dental pulp tissue engineering in full-length human root canals. J Dent Res 2013;92:970-5.
  • [6] Kelm JM, Fussenegger M. Microscale tissue engineering using gravity-enforced cell assembly. Trends Biotechnol. 2004;22:195-202.
  • [7] Kelm JM, Djonov V, Ittner LM, Fluri D, Born W, Hoerstrup SP, et al. Design of custom-shaped vascularized tissues using microtissue spheroids as minimal building units. Tissue Eng 2006;12:2151-60.
  • [8] Rouwkema J, Rivron NC, van Blitterswijk CA. Vascularization in tissue engineering. Trends Biotechnol 2008;26:434-41.
  • [9] Dissanayaka W, Zhu L, Hargreaves K, Jin L, Zhang C. Scaffold-free prevascularized microtissue spheroids for pulp regeneration. J Dent Res 2014;93:1296-303.
  • [10] Mendicino M, Bailey AM, Wonnacott K, Puri RK, Bauer SR. MSC-based product characterization for clinical trials: an FDA perspective. Cell Stem Cell 2014;14:141-5.
  • [11] Karnieli O, Friedner OM, Allickson JG, Zhang N, Jung S, Fiorentini D, et al. A consensus introduction to serum replacements and serum-free media for cellular therapies. Cytotherapy 2017;19:155-69.
  • [12] Yu M, Bardia A, Aceto N, Bersani F, Madden MW, Donaldson MC, et al. Cancer therapy. Ex vivo culture of circulating breast tumor cells for individualized testing of drug susceptibility. Science 2014;345:216-20.
  • [13] Kim CS, Mout R, Zhao Y, Yeh Y-C, Tang R, Jeong Y, et al. Co-delivery of protein and small molecule therapeutics using nanoparticle-stabilized nanocapsules. Bioconjug Chem 2015;26:950-4.
  • [14] Rouwkema J, Khademhosseini A. Vascularization and angiogenesis in tissue engineering: beyond creating static networks. Trends Biotechnol 2016;34:733-45.
  • [15] Karaman O, Onak G, Demirci EA, Kahraman E. Integrin binding peptide promotes in vitro wound closure in the L929 mouse fibroblasts. Eur Res J 2017;3:207-13.
  • [16] Gstraunthaler G, Lindl T, van der Valk J. A plea to reduce or replace fetal bovine serum in cell culture media. Cytotechnology 2013;65:791-3.
  • [17] Napolitano AP, Dean DM, Man AJ, Youssef J, Ho DN, Rago AP, et al. Scaffold-free three-dimensional cell culture utilizing micromolded nonadhesive hydrogels. Biotechniques 2007;43:494-500.
  • [18] Sanz-Nogués C, O’Brien T. In vitro models for assessing therapeutic angiogenesis. Drug Discov Today 2016;21:1495-503.
There are 18 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Original Articles
Authors

Ozan Karaman 0000-0002-4175-4402

Ziyşan Buse Yaralı 0000-0002-9371-6424

Publication Date July 4, 2018
Submission Date October 6, 2017
Acceptance Date December 2, 2017
Published in Issue Year 2018

Cite

AMA Karaman O, Yaralı ZB. Determination of minimum serum concentration to develop scaffold free micro-tissue. Eur Res J. July 2018;4(3):145-151. doi:10.18621/eurj.342109

e-ISSN: 2149-3189 


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