Papers

Peer-reviewed International journal
Jun 22, 2015

Peptide-modified Substrate for Modulating Gland Tissue Growth and Morphology In Vitro.

Scientific reports
  • Hiroaki Taketa
  • ,
  • Gulsan Ara Sathi
  • ,
  • Mahmoud Farahat
  • ,
  • Kazi Anisur Rahman
  • ,
  • Takayoshi Sakai
  • ,
  • Yoshiaki Hirano
  • ,
  • Takuo Kuboki
  • ,
  • Yasuhiro Torii
  • ,
  • Takuya Matsumoto

Volume
5
Number
First page
11468
Last page
11468
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1038/srep11468

In vitro fabricated biological tissue would be a valuable tool to screen newly synthesized drugs or understand the tissue development process. Several studies have attempted to fabricate biological tissue in vitro. However, controlling the growth and morphology of the fabricated tissue remains a challenge. Therefore, new techniques are required to modulate tissue growth. RGD (arginine-glycine-aspartic acid), which is an integrin-binding domain of fibronectin, has been found to enhance cell adhesion and survival; it has been used to modify substrates for in vitro cell culture studies or used as tissue engineering scaffolds. In addition, this study shows novel functions of the RGD peptide, which enhances tissue growth and modulates tissue morphology in vitro. When an isolated submandibular gland (SMG) was cultured on an RGD-modified alginate hydrogel sheet, SMG growth including bud expansion and cleft formation was dramatically enhanced. Furthermore, we prepared small RGD-modified alginate beads and placed them on the growing SMG tissue. These RGD-modified beads successfully induced cleft formation at the bead position, guiding the desired SMG morphology. Thus, this RGD-modified material might be a promising tool to modulate tissue growth and morphology in vitro for biological tissue fabrication.

Link information
DOI
https://doi.org/10.1038/srep11468
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26098225
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476418
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000356595900001&DestApp=WOS_CPL
ID information
  • DOI : 10.1038/srep11468
  • ISSN : 2045-2322
  • Pubmed ID : 26098225
  • Pubmed Central ID : PMC4476418
  • Web of Science ID : WOS:000356595900001

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