研究目的
Investigating the temporal and spatial evolution of extracellular pH (pHe) during cell apoptosis using surface-enhanced Raman spectroscopy (SERS).
研究成果
The developed SERS-based method allows in situ monitoring of pHe of single living cells, showing potential for understanding cellular processes on the single cell level. The method demonstrated differences in pHe between cancer and normal cells and tracked pHe changes during apoptosis induced by TGF-β.
研究不足
The study is limited to in vitro conditions and specific cell lines. The spatial resolution and sensitivity of SERS may vary with different substrates and experimental conditions.
1:Experimental Design and Method Selection:
The study used 4-MPy modified Au nanoparticles-assembled solid SERS substrate for in situ pHe sensing.
2:Sample Selection and Data Sources:
Human tongue squamous carcinoma cells (SCC-4, TCA-8113A cell line) and mouse calvaria osteoblast precursor cells (MC3T3-E1 cell line) were cultured.
3:List of Experimental Equipment and Materials:
Au nanoparticles, 4-MPy, TGF-β, SEM, UV?vis spectrometer, Nanophoton Raman-11 system.
4:Experimental Procedures and Operational Workflow:
Cells were cultured on the substrate, and pHe was monitored before and after TGF-β addition.
5:Data Analysis Methods:
SERS spectra were analyzed for pH response, and statistical histogram analysis was performed for pH distribution.
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