4.7 Article

Three-dimensional imaging of lipids and metabolites in tissues by nanospray desorption electrospray ionization mass spectrometry

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 407, 期 8, 页码 2063-2071

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-014-8174-0

关键词

Three-dimensional (3D) imaging mass spectrometry; Nanospray desorption electrospray ionization (nano-DESI); Mouse embryo; Phospholipids; Metabolites

资金

  1. US Department of Energy (DOE) [DE-AC05-76RL01830]
  2. DOE's Office of Biological and Environmental Research
  3. NIH [HD068524, DA06668]
  4. March of Dimes
  5. Ruth L. Kirschstein Predoctoral NRSA Fellowship [F30AG040858]

向作者/读者索取更多资源

Three-dimensional (3D) imaging of tissue sections is a new frontier in mass spectrometry imaging (MSI). Here, we report on fast 3D imaging of lipids and metabolites associated with mouse uterine decidual cells and embryo at the implantation site on day 6 of pregnancy. 2D imaging of 16-20 serial tissue sections deposited on the same glass slide was performed using nanospray desorption electrospray ionization (nano-DESI)-an ambient ionization technique that enables sensitive localized analysis of analytes on surfaces without special sample pretreatment. In this proof-of-principle study, nano-DESI was coupled to a high-resolution Q-Exactive instrument operated at high repetition rate of > 5 Hz with moderate mass resolution of 35,000 (m/Delta m at m/z 200), which enabled acquisition of the entire 3D image with a spatial resolution of similar to 150 mu m in less than 4.5 h. The results demonstrate localization of acetylcholine in the primary decidual zone (PDZ) of the implantation site throughout the depth of the tissue examined, indicating an important role of this signaling molecule in decidualization. Choline and phosphocholine-metabolites associated with cell growth-are enhanced in the PDZ and abundant in other cellular regions of the implantation site. Very different 3D distributions were obtained for fatty acids (FA), oleic acid and linoleic acid (FA 18:1 and FA 18:2), differing only by one double bond. Localization of FA 18:2 in the PDZ indicates its important role in decidualization while FA 18:1 is distributed more evenly throughout the tissue. In contrast, several lysophosphatidylcholines (LPC) observed in this study show donut-like distributions with localization around the PDZ. Complementary distributions with minimal overlap were observed for LPC 18:0 and FA 18:2 while the 3D image of the potential precursor phosphatidylcholine 36:2 (PC 36:2) showed a significant overlap with both LPC 18:0 and FA 18:2.

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