Zur Hauptnavigation wechseln Zur Suche wechseln Zum Hauptinhalt wechseln

Gelatin-Methacryloyl (GelMA) Formulated with Human Platelet Lysate Supports Mesenchymal Stem Cell Proliferation and Differentiation and Enhances the Hydrogel’s Mechanical Properties

  • Marline Kirsch
  • , Luise Birnstein
  • , Iliyana Pepelanova
  • , Wiebke Handke
  • , Jessica Rach
  • , Axel Seltsam
  • , Thomas Scheper
  • , Antonina Lavrentieva*
  • *Korrespondierende*r Autor*in für diese Arbeit

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Abstract

Three-dimensional (3D) cell culture is a major focus of current research, since cultivation under physiological conditions provides more reliable information about in vivo cell behavior. 3D cell cultures are used in basic research to better understand intercellular and cell-matrix interactions. However, 3D cell culture plays an increasingly important role in the in vitro testing of bioactive substances and tissue engineering. Gelatin-methacryloyl (GelMA) hydrogels of different degrees of functionalization (DoFs) are a versatile tool for 3D cell culture and related applications such as bioprinting. Human platelet lysate (hPL) has already demonstrated positive effects on 2D cell cultures of different cell types and has proven a valuable alternative to fetal calf serum (FCS). Traditionally, all hydrogels are formulated using buffers. In this study, we supplemented GelMA hydrogels of different DoF with hPL during adipose tissue-derived mesenchymal stem cell (AD-MSCs) encapsulation. We studied the effect of hPL supplementation on the spreading, proliferation, and osteogenic differentiation of AD-MSCs. In addition, the influence of hPL on hydrogel properties was also investigated. We demonstrate that the addition of hPL enhanced AD-MSC spreading, proliferation, and osteogenic differentiation in a concentration-dependent manner. Moreover, the addition of hPL also increased GelMA viscosity and stiffness.

OriginalspracheEnglisch
Aufsatznummer76
FachzeitschriftBioengineering
Jahrgang6
Ausgabenummer3
Elektronisch veröffentlicht (E-Pub)28 Aug. 2019
DOIs
PublikationsstatusVeröffentlicht - Sept. 2019

ASJC Scopus Sachgebiete

  • Bioengineering

Dieses zitieren