Journal
LANGMUIR
Volume 29, Issue 24, Pages 7362-7368Publisher
AMER CHEMICAL SOC
DOI: 10.1021/la303459v
Keywords
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Funding
- Funding Program for Next Generation World-Leading Researchers (NEXT Program) [LR026]
- Japan Society for the Promotion of Science (JSPS) [A232250040]
- Grants-in-Aid for Scientific Research [23225004] Funding Source: KAKEN
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In recent approaches to tissue engineering, cells face various stresses from physical, chemical, and environmental stimuli. For example, coating cell membranes with nanofilms using layer-by-layer (LbL) assembly requires many cycles of centrifugation, causing physical (gravity) stress. Damage to cell membranes can cause the leakage of cytosol molecules or sometimes cell death. Accordingly, we evaluated the effectiveness of LbL films prepared on cell membranes in protecting cells from physical stresses. After two steps of LbL assembly using Tris-HCl buffer solution without polymers or proteins (four centrifugation cycles including washing), hepatocyte carcinoma (HepG2) cells showed extremely high cell death and the viability was ca. 15%. Their viability ultimately decreased to 6% after 9 steps of LbL assembly (18 cycles of centrifugation), which is the typical number of steps involved in preparing LbL nanofilms. However, significantly higher viability (>85%) of HepG2 cells was obtained after nine steps of LbL assembly employing fibronectin (FN)-gelatin (G) or type IV collagen (Col IV)-laminin (LN) solution combinations, which are typical components of an extracellular matrix (ECM), to fabricate 10-nm-thick LbL films. When LbL films of synthetic polymers created via electrostatic interactions were employed instead of the ECM films described above, the viability of the HepG2 cells after the same nine steps slightly decreased to 61%. The protective effects of LbL films were strongly dependent on their thickness, and the critical thickness was >5 nm. Surprisingly, a high viability of over 85% was achieved even under extreme physical stress conditions (10 000 rpm). We evaluated the leakage of lactate dehydrogenase (LDH) during the LbL assembly processes to clarify the protective effect, and a reduction in LDH leakage was clearly observed when using FN-G nanofilms. Moreover, the LbL films do not inhibit cell growth during cell culturing, suggesting that these coated cells can be useful for other experiments. LbL nanofilm coatings, especially ECM nanofilm coatings, will be important techniques for protecting cell membranes from physical stress during tissue engineering.
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