Engineering a platform combining decellularized ECM and native bone surface topography for investigating osteoblastic function


Erenay B., Özçolak B., Öztatlı H., Erkoç-Biradlı F. Z., Jandt K. D., ODABAŞ S., ...More

Biomedical Materials (Bristol), vol.21, no.1, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Publication Type: Article / Article
  • Volume: 21 Issue: 1
  • Publication Date: 2026
  • Doi Number: 10.1088/1748-605x/ae2558
  • Journal Name: Biomedical Materials (Bristol)
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Chemical Abstracts Core, Compendex, EMBASE, INSPEC, MEDLINE
  • Keywords: biomimetics, cell-derived decellularized ECM, osteogenic function, surface topography
  • Ankara University Affiliated: Yes

Abstract

Utilization of cell derived decellularized extracellular matrices (dECM) is a highly versatile way to introduce complex cell specific native-like microenvironment in vitro. While dECMs have been used in various applications, surface functionalization of biomaterials with cell-derived dECMs that maintain their structural integrity for investigating cell behavior is rarely reported. This study aims to create a biomimetic platform by combining pre-osteoblast derived dECM with native bone surface topography mimicked (BSM) polydimethylsiloxane (PDMS) for in vitro investigation of osteoblastic function. Decellularized extracellular matrix on PDMS and BSM PDMS surfaces preserved their structure and specific matrix components, in addition to having a significant influence on microscale surface topography. Recellularization of BSM PDMS + dECM surfaces supported cell attachment and proliferation of both pre-osteoblasts and human adipose derived mesenchymal stem cells (hADMSCs). BSM PDMS + dECM surfaces showed significantly elevated glycosaminoglycan content, as well as resulted in induction and topography dependent calcification of hADMSCs. Osteogenic induction and dECM presence on BSM PDMS synergistically increased RUNX2 expression of hADMSCs while not having an effect on YAP expression. This work provides insights for designing biomimetic platforms integrating biochemical and biophysical cues for advanced bone tissue engineering.