4.7 Article

Determining the stages of cellular differentiation using deep ultraviolet resonance Raman spectroscopy

期刊

TALANTA
卷 227, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2021.122164

关键词

Deep-ultraviolet Raman resonance spectroscopy; Vibrational spectroscopy; Myoblasts; Cellular differentiation; Chemometrics

资金

  1. SUNY startup
  2. American Heart Association [AHA 17SDG33670339]
  3. National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIAMS [R15AR074728]
  4. NIH training Grant [T32 GM13206]
  5. Government of the Russian Federation [N.2020-220-08-2389]

向作者/读者索取更多资源

Cellular differentiation is a crucial biological process that starts from embryonic development and continues into adulthood. Using deep ultraviolet resonance Raman spectroscopy in combination with chemometric techniques, different stages of cellular differentiation can be easily distinguished, offering great potential for detecting abnormal cellular differentiation in pathological conditions in the future.
Cellular differentiation is a fundamental process in which one cell type changes into one or more specialized cell types. Cellular differentiation starts at the beginning of embryonic development when a simple zygote begins to transform into a complex multicellular organism composed of various cell and tissue types. This process continues into adulthood when adult stem cells differentiate into more specialized cells for normal growth, regeneration, repair, and cellular turnover. Any abnormalities associated with this fundamental process of cellular differentiation are linked to life-threatening conditions, including degenerative diseases and cancers. Detection of undifferentiated and different stages of differentiated cells can be used for disease diagnosis but is often challenging due to the laborious procedures, expensive tools, and specialized technical skills which are required. Here, a novel approach, called deep ultraviolet resonance Raman spectroscopy, is used to study various stages of cellular differentiation using a well-known myoblast cell line as a model system. These cells proliferate in the growth medium and spontaneously differentiate in differentiation medium into myocytes and later into myotubes. The cellular and molecular characteristics of these cells mimic very well actual muscle tissue in vivo. We have found that undifferentiated myoblast cells and myoblast cells differentiated at three different stages are able to be easily separated using deep ultraviolet resonance Raman spectroscopy in combination with chemometric techniques. Our study has a great potential to study cellular differentiation during normal development as well as to detect abnormal cellular differentiation in human pathological conditions in future studies.

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