Capillary-like formations of endothelial cells in defined patterns generated by laser bioprinting

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Lothar Koch
  • Andrea Deiwick
  • Boris Chichkov

Research Organisations

External Research Organisations

  • NIFE - Lower Saxony Centre for Biomedical Engineering, Implant Research and Development
View graph of relations

Details

Original languageEnglish
Article number1538
JournalMicromachines
Volume12
Issue number12
Publication statusPublished - 10 Dec 2021

Abstract

Bioprinting is seen as a promising technique for tissue engineering, with hopes of one day being able to produce whole organs. However, thick tissue requires a functional vascular network, which naturally contains vessels of various sizes, down to capillaries of ~10 µm in diameter, often spaced less than 200 µm apart. If such thick tissues are to be printed, the vasculature would likely need to be printed at the same time, including the capillaries. While there are many approaches in tissue engineering to produce larger vessels in a defined manner, the small capillaries usually arise only in random patterns by sprouting from the larger vessels or from randomly distributed endothelial cells. Here, we investigated whether the small capillaries could also be printed in predefined patterns. For this purpose, we used a laser-based bioprinting technique that allows for the combination of high resolution and high cell density. Our aim was to achieve the formation of closed tubular structures with lumina by laser-printed endothelial cells along the printed patterns on a surface and in bioprinted tissue. This study shows that such capillaries are directly printable; however, persistence of the printed tubular structures was achieved only in tissue with external stimulation by other cell types.

Keywords

    Biofabrication, Bioprinting, Capillaries, Endothelial cells, Laser, Tissue engineering, Vascularization

ASJC Scopus subject areas

Cite this

Capillary-like formations of endothelial cells in defined patterns generated by laser bioprinting. / Koch, Lothar; Deiwick, Andrea; Chichkov, Boris.
In: Micromachines, Vol. 12, No. 12, 1538, 10.12.2021.

Research output: Contribution to journalArticleResearchpeer review

Koch L, Deiwick A, Chichkov B. Capillary-like formations of endothelial cells in defined patterns generated by laser bioprinting. Micromachines. 2021 Dec 10;12(12):1538. doi: 10.3390/mi12121538
Koch, Lothar ; Deiwick, Andrea ; Chichkov, Boris. / Capillary-like formations of endothelial cells in defined patterns generated by laser bioprinting. In: Micromachines. 2021 ; Vol. 12, No. 12.
Download
@article{8bc92257afc3439889abf0997a9d1ef5,
title = "Capillary-like formations of endothelial cells in defined patterns generated by laser bioprinting",
abstract = "Bioprinting is seen as a promising technique for tissue engineering, with hopes of one day being able to produce whole organs. However, thick tissue requires a functional vascular network, which naturally contains vessels of various sizes, down to capillaries of ~10 µm in diameter, often spaced less than 200 µm apart. If such thick tissues are to be printed, the vasculature would likely need to be printed at the same time, including the capillaries. While there are many approaches in tissue engineering to produce larger vessels in a defined manner, the small capillaries usually arise only in random patterns by sprouting from the larger vessels or from randomly distributed endothelial cells. Here, we investigated whether the small capillaries could also be printed in predefined patterns. For this purpose, we used a laser-based bioprinting technique that allows for the combination of high resolution and high cell density. Our aim was to achieve the formation of closed tubular structures with lumina by laser-printed endothelial cells along the printed patterns on a surface and in bioprinted tissue. This study shows that such capillaries are directly printable; however, persistence of the printed tubular structures was achieved only in tissue with external stimulation by other cell types.",
keywords = "Biofabrication, Bioprinting, Capillaries, Endothelial cells, Laser, Tissue engineering, Vascularization",
author = "Lothar Koch and Andrea Deiwick and Boris Chichkov",
note = "Funding Information: Funding: The research presented here was funded by European Union{\textquoteright}s Horizon 2020 project PLATFORMA, Grant 951890, and German Cluster of Excellence Ex62/2 Rebirth.",
year = "2021",
month = dec,
day = "10",
doi = "10.3390/mi12121538",
language = "English",
volume = "12",
journal = "Micromachines",
issn = "2072-666X",
publisher = "Multidisciplinary Digital Publishing Institute",
number = "12",

}

Download

TY - JOUR

T1 - Capillary-like formations of endothelial cells in defined patterns generated by laser bioprinting

AU - Koch, Lothar

AU - Deiwick, Andrea

AU - Chichkov, Boris

N1 - Funding Information: Funding: The research presented here was funded by European Union’s Horizon 2020 project PLATFORMA, Grant 951890, and German Cluster of Excellence Ex62/2 Rebirth.

PY - 2021/12/10

Y1 - 2021/12/10

N2 - Bioprinting is seen as a promising technique for tissue engineering, with hopes of one day being able to produce whole organs. However, thick tissue requires a functional vascular network, which naturally contains vessels of various sizes, down to capillaries of ~10 µm in diameter, often spaced less than 200 µm apart. If such thick tissues are to be printed, the vasculature would likely need to be printed at the same time, including the capillaries. While there are many approaches in tissue engineering to produce larger vessels in a defined manner, the small capillaries usually arise only in random patterns by sprouting from the larger vessels or from randomly distributed endothelial cells. Here, we investigated whether the small capillaries could also be printed in predefined patterns. For this purpose, we used a laser-based bioprinting technique that allows for the combination of high resolution and high cell density. Our aim was to achieve the formation of closed tubular structures with lumina by laser-printed endothelial cells along the printed patterns on a surface and in bioprinted tissue. This study shows that such capillaries are directly printable; however, persistence of the printed tubular structures was achieved only in tissue with external stimulation by other cell types.

AB - Bioprinting is seen as a promising technique for tissue engineering, with hopes of one day being able to produce whole organs. However, thick tissue requires a functional vascular network, which naturally contains vessels of various sizes, down to capillaries of ~10 µm in diameter, often spaced less than 200 µm apart. If such thick tissues are to be printed, the vasculature would likely need to be printed at the same time, including the capillaries. While there are many approaches in tissue engineering to produce larger vessels in a defined manner, the small capillaries usually arise only in random patterns by sprouting from the larger vessels or from randomly distributed endothelial cells. Here, we investigated whether the small capillaries could also be printed in predefined patterns. For this purpose, we used a laser-based bioprinting technique that allows for the combination of high resolution and high cell density. Our aim was to achieve the formation of closed tubular structures with lumina by laser-printed endothelial cells along the printed patterns on a surface and in bioprinted tissue. This study shows that such capillaries are directly printable; however, persistence of the printed tubular structures was achieved only in tissue with external stimulation by other cell types.

KW - Biofabrication

KW - Bioprinting

KW - Capillaries

KW - Endothelial cells

KW - Laser

KW - Tissue engineering

KW - Vascularization

UR - http://www.scopus.com/inward/record.url?scp=85121618778&partnerID=8YFLogxK

U2 - 10.3390/mi12121538

DO - 10.3390/mi12121538

M3 - Article

AN - SCOPUS:85121618778

VL - 12

JO - Micromachines

JF - Micromachines

SN - 2072-666X

IS - 12

M1 - 1538

ER -