细胞外基质
背景(考古学)
生物
转录组
计算生物学
细胞生物学
蛋白质组学
系统生物学
基因表达
遗传学
基因
古生物学
作者
Grace C. Bingham,Fred Lee,Alexandra Naba,Thomas H. Barker
出处
期刊:Matrix Biology
[Elsevier BV]
日期:2020-09-01
卷期号:91-92: 152-166
被引量:59
标识
DOI:10.1016/j.matbio.2020.04.004
摘要
Complex intercellular interactions as well as biomolecular and biomechanical cues from the extracellular matrix (ECM) profoundly affect cellular functions. Traditional transcriptomic and proteomic approaches have provided insight into disease progression by identifying discrete cellular subpopulations or microenvironmental signatures characteristic of normal or pathological tissues, however these techniques do not examine how a given cellular state relates to its interactions with neighboring cells or its surrounding ECM with multiparametric characterization (i.e. ECM alignment, mechanical forces, crosslinking, etc.). Emerging spatial-omic techniques can provide high-resolution mapping of expression profiles similar to scRNA-seq and mass spectroscopy directly within tissues. The ability to preserve the spatial context of cells within samples, their cellular geometry, as well as their surrounding ECM gives spatial-omics the opportunity to interrogate previously unexplored signaling modalities, which has the potential to revolutionize ECM research and our understanding of fibrotic diseases. In this review, we present current spatial transcriptomic and proteomic techniques and discuss how they may be applied to investigate cell-ECM interactions.
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