TY - JOUR
T1 - Convenient rapid prototyping microphysiological niche for mimicking liver native basement membrane
T2 - Liver sinusoid on a chip
AU - Ebrahimi, Aliakbar
AU - Ghorbanpoor, Hamed
AU - Apaydın, Elif
AU - Demir Cevizlidere, Bahar
AU - Özel, Ceren
AU - Tüfekçioğlu, Emre
AU - Koç, Yücel
AU - Topal, Ahmet Emin
AU - Tomsuk, Özlem
AU - Güleç, Kadri
AU - Abdullayeva, Nuran
AU - Kaya, Murat
AU - Ghorbani, Aynaz
AU - Şengel, Tayfun
AU - Benzait, Zineb
AU - Uysal, Onur
AU - Eker Sarıboyacı, Ayla
AU - Doğan Güzel, Fatma
AU - Singh, Hemant
AU - Hassan, Shabir
AU - Ankara, Hüseyin
AU - Pat, Suat
AU - Atalay, Eray
AU - Avci, Huseyin
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2025/1
Y1 - 2025/1
N2 - Liver is responsible for the metabolization processes of up to 90 % of compounds and toxins in the body. Therefore liver-on-a-chip systems, as an in vitro promising cell culture platform, have great importance for fundamental science and drug development. In most of the liver-on-a-chip studies, seeding cells on both sides of a porous membrane, which represents the basement membrane, fail to resemble the native characteristics of biochemical, biophysical, and mechanical properties. In this study, polycarbonate (PC) and polyethylene terephthalate (PET) membranes were coated with gelatin to address this issue by accurately mimicking the native basement membrane present in the space of Disse. Various coating methods were used, including doctor blade, gel micro-injection, electrospinning, and spin coating. Spin coating was demonstrated to be the most effective technique owing to the ability to produce thin gel thickness with desirable surface roughness for cell interactions on both sides of the membrane. HepG2 and EA.HY926 cells were seeded on the upper and bottom sides of the gelatin-coated PET membrane and cultured on-chip for 7 days. Cell viability increased from 90 % to 95 %, while apoptotic index decreased. Albumin secretion notably rose between days 1–7 and 4–7, while GST-α secretion decreased from day 1 to day 7. In conclusion, the optimized spin coating process reported here can effectively modify the membranes to better mimic the native basement membrane niche characteristics.
AB - Liver is responsible for the metabolization processes of up to 90 % of compounds and toxins in the body. Therefore liver-on-a-chip systems, as an in vitro promising cell culture platform, have great importance for fundamental science and drug development. In most of the liver-on-a-chip studies, seeding cells on both sides of a porous membrane, which represents the basement membrane, fail to resemble the native characteristics of biochemical, biophysical, and mechanical properties. In this study, polycarbonate (PC) and polyethylene terephthalate (PET) membranes were coated with gelatin to address this issue by accurately mimicking the native basement membrane present in the space of Disse. Various coating methods were used, including doctor blade, gel micro-injection, electrospinning, and spin coating. Spin coating was demonstrated to be the most effective technique owing to the ability to produce thin gel thickness with desirable surface roughness for cell interactions on both sides of the membrane. HepG2 and EA.HY926 cells were seeded on the upper and bottom sides of the gelatin-coated PET membrane and cultured on-chip for 7 days. Cell viability increased from 90 % to 95 %, while apoptotic index decreased. Albumin secretion notably rose between days 1–7 and 4–7, while GST-α secretion decreased from day 1 to day 7. In conclusion, the optimized spin coating process reported here can effectively modify the membranes to better mimic the native basement membrane niche characteristics.
KW - Co-culture
KW - EA.HY926
KW - HepG2
KW - Liver-on-a-chip
KW - Space of disse
KW - Spin coating
UR - https://www.scopus.com/pages/publications/85205713417
U2 - 10.1016/j.colsurfb.2024.114292
DO - 10.1016/j.colsurfb.2024.114292
M3 - Article
C2 - 39383580
AN - SCOPUS:85205713417
SN - 0927-7765
VL - 245
JO - Colloids and Surfaces B: Biointerfaces
JF - Colloids and Surfaces B: Biointerfaces
M1 - 114292
ER -