Insilico and Electron Microscope Study about Attachment of Mesenchymal Stem Cell Derived from Stromal Vascular Fraction to Scaffold (Bovine Bone Cancellous, Hydroxyapatite-Calcium Sulphate, Calcium Phosphate)

Panji Sananta

Abstract

Objective: Insilico study using molecular docking with Hex had already surpassed all of the other previous approach in assessment of molecular binding to scaffold. The combination of insilico study to investigate the molecular binding to scaffold and electron microscope to assess the population density of adipocyte derivative stem cells by measuring the number of cluster cells could show the inter cell communication between adipocyte derived stem cell and scaffold. The aim of this study is to prove the attachment of mesenchymal stem cell (MSC) from stromal vascular fraction (SVF) to scaffold.

Methods: The research is true experimental research using molecular docking with HEX version 8.0. Electron microscope used to measure the density and number of cluster cells of adipocyte derivative stem cells.

Results: The strongest bound to scaffold is between MSC from SVF to hydroxyapatite in both receptor which was Integrin Alpha V to Hydroxyapatite which need a total energy of -89.24 (J/Mol) and Integrin Beta 2 to Hydroxyapatite which need a total energy of -177.8 (J/Mol). The highest impact obtained from hydroxyapatite-calcium phosphate with an average value of 12.66 cluster cells counting per 100 µm2 scaffold material observed by electron microscope.

Conclusion: This study showed that MSC from SVF could attach to scaffold with stronger binding between Integrin Alpha V and Integrin Beta 2 to hydroxyapatite. From microscope electron study we can prove that MSC can make a cluster cell in those scaffolds with hydroxyapatite-calcium sulphate having the biggest cluster cell counting.

Keywords: Hydroxyapatite; Integrin Alpha V; Integrin Beta 2; Mesenchymal stem cell; Scanning electron microscope; Stromal vascular fraction.

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References

Eltom Abdalla, Zhong Gaoyan, and Muhammad Ameen. Scaffold Techniques and Designs in Tissue Engineering Functions and Purposes: A Review. Advances in Materials Sciences and Engineering. 2019. Page 1-13.

Tatara Alexander M., Mikos Antonios G. Tissue Engineering in Orthopaedics. The Journal of Bone and Joint Surgery. 2016. 98: 1132-9.

Ramakrishnan VM, Boyd NL. The Adipose Stromal Vascular Fraction as a Complex Cellular Source for Tissue Engineering Appications. Tissue Eng Part B Rev. 2018. 24(4): 289-299.

Mankos M., Shadman K., Persson H.H.J., N’Diaye A.T.N., Schmid A.K., Davis R.W. A Novel Low Energy Electron Microscope for DNA Sequencing and Surface Analysis. Ultramicroscopy. 2014. 145: 36-49.

Ritchie D.W. Recent progress and future directions in protein-protein docking. Curr Prot Pep Sci. 2008. 9(1): 1-15.

Kim K, Dean D, Mikos AG, Fisher JP. Effect of initial cell seeding density on early osteogenic signal expression of rat bone marrow stromal cells cultured on cross-linked poly (propylene fumarate) disks. Biomacromolecules. 2009. 10:1810-17.

Macindoe Gary, Mavridis Lazaros, Venkatraman Vishwesh, Devignes Marie-Dominique, and Ritchie David W. HexServer: an FFT-based protein docking server powered by graphics processors. Nucleic Acids Research. 2010. 38: W445-W449.

Mahmood Saffanah Khuder, Zakaria Md Zuki Abu Bakar, Razak Intan Shameha Binti Abdul, Yusof Loqman Mohamed, Jaji Alhaji Zubair, Tijani Isa, Hammadi Nahidah Ibrahim. Preparation and characterization of cockle shell aragonite nanocomposite porous 3D scaffolds for bone repair. Biochemistry and Biophysics Reports. 2017. 10: 237-251.

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