4.8 Article

Identifying Individual Cell Types in Heterogeneous Cultures Using Secondary Ion Mass Spectrometry Imaging with C60 Etching and Multivariate Analysis

期刊

ANALYTICAL CHEMISTRY
卷 84, 期 2, 页码 893-900

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac201179t

关键词

-

资金

  1. National ESCA
  2. Surface Analysis Center for Biomedical Problems (NESAC/BIO) through National Institutes of Health at the University of Washington [EB-002027]
  3. University of Washington Engineered Biomaterials 21st Century (UWEB21) center, an Engineering Research Center

向作者/读者索取更多资源

Tissue engineering approaches fabricate and subsequently, implant cell-seeded and unseeded scaffold biomaterials. Once in the body, these biomaterials are repopulated with somatic cells of various phenotypes whose identification upon explantation can be expensive and time-consuming. We show that imaging time-of-flight secondary ion mass spectrometry (TOF-SIMS) can be used to distinguish mammalian cell types in heterogeneous cultures. Primary rat esophageal epithelial cells (REEC) were cultured with NIH 3T3 mouse fibroblasts on tissue culture polystyrene and freeze-dried before TOF-SIMS imaging. Results show that a short etching sequence with C-60(+) can be used to clean the sample surface and improve the TOF-SIMS image quality. Principal component analysis (PCA) and partial least-squares discriminant analysis (PLS-DA) were used to identify peaks whose contributions to the total variance in the multivariate model Were due to either the two cell types or the substrate. Using PLS-DA, unknown regions of cellularity that were otherwise unidentifiable by SIMS could be classified. From the loadings in the PLS-DA model, peaks were selected that were indicative of the two cell types and TOF-SIMS images were created and overlaid that showed the ability of this method to distinguish features visually..

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据