Mesenchymal stem cell 3D encapsulation technologies for biomimetic microenvironment in tissue regeneration

Hyerim Kim, Chaewon Bae, Yun Min Kook, Won Gun Koh, Kangwon Lee, Min Hee Park

Research output: Contribution to journalReview article

4 Citations (Scopus)

Abstract

Mesenchymal stem cell (MSC) encapsulation technique has long been emerged in tissue engineering as it plays an important role in implantation of stem cells to regenerate a damaged tissue. MSC encapsulation provides a mimic of a three-dimensional (3D) in vivo environment to maintain cell viability and to induce the stem cell differentiation which regulates MSC fate into multi-lineages. Moreover, the 3D matrix surrounding MSCs protects them from the human innate immune system and allows the diffusion of biomolecules such as oxygen, cytokines, and growth factors. Therefore, many technologies are being developed to create MSC encapsulation platforms with diverse materials, shapes, and sizes. The conditions of the platform are determined by the targeted tissue and translation method. This review introduces several details of MSC encapsulation technologies such as micromolding, electrostatic droplet extrusion, microfluidics, and bioprinting and their application for tissue regeneration. Lastly, some of the challenges and future direction of MSC encapsulation technologies as a cell therapy-based tissue regeneration method will be discussed.

Original languageEnglish
Article number51
JournalStem Cell Research and Therapy
Volume10
Issue number1
DOIs
Publication statusPublished - 2019 Feb 7

Fingerprint

Tissue regeneration
Biomimetics
Stem cells
Mesenchymal Stromal Cells
Encapsulation
Regeneration
Technology
Bioprinting
Stem Cells
Microfluidics
Tissue Engineering
Tissue
Cell- and Tissue-Based Therapy
Static Electricity
Cell Differentiation
Immune system
Immune System
Cell Survival
Intercellular Signaling Peptides and Proteins
Biomolecules

All Science Journal Classification (ASJC) codes

  • Medicine (miscellaneous)
  • Molecular Medicine
  • Biochemistry, Genetics and Molecular Biology (miscellaneous)
  • Cell Biology

Cite this

Kim, Hyerim ; Bae, Chaewon ; Kook, Yun Min ; Koh, Won Gun ; Lee, Kangwon ; Park, Min Hee. / Mesenchymal stem cell 3D encapsulation technologies for biomimetic microenvironment in tissue regeneration. In: Stem Cell Research and Therapy. 2019 ; Vol. 10, No. 1.
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Mesenchymal stem cell 3D encapsulation technologies for biomimetic microenvironment in tissue regeneration. / Kim, Hyerim; Bae, Chaewon; Kook, Yun Min; Koh, Won Gun; Lee, Kangwon; Park, Min Hee.

In: Stem Cell Research and Therapy, Vol. 10, No. 1, 51, 07.02.2019.

Research output: Contribution to journalReview article

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T1 - Mesenchymal stem cell 3D encapsulation technologies for biomimetic microenvironment in tissue regeneration

AU - Kim, Hyerim

AU - Bae, Chaewon

AU - Kook, Yun Min

AU - Koh, Won Gun

AU - Lee, Kangwon

AU - Park, Min Hee

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Y1 - 2019/2/7

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AB - Mesenchymal stem cell (MSC) encapsulation technique has long been emerged in tissue engineering as it plays an important role in implantation of stem cells to regenerate a damaged tissue. MSC encapsulation provides a mimic of a three-dimensional (3D) in vivo environment to maintain cell viability and to induce the stem cell differentiation which regulates MSC fate into multi-lineages. Moreover, the 3D matrix surrounding MSCs protects them from the human innate immune system and allows the diffusion of biomolecules such as oxygen, cytokines, and growth factors. Therefore, many technologies are being developed to create MSC encapsulation platforms with diverse materials, shapes, and sizes. The conditions of the platform are determined by the targeted tissue and translation method. This review introduces several details of MSC encapsulation technologies such as micromolding, electrostatic droplet extrusion, microfluidics, and bioprinting and their application for tissue regeneration. Lastly, some of the challenges and future direction of MSC encapsulation technologies as a cell therapy-based tissue regeneration method will be discussed.

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