Chemical imaging of cardiac cell and tissue by using secondary ion mass spectrometry

Mol Imaging Biol. 2011 Dec;13(6):1067-76. doi: 10.1007/s11307-010-0460-4.

Abstract

Purpose: Identification and localization of biomolecules in cells and tissue samples are important for understanding of subcellular structures and can be helpful in biomedical and pharmaceutical research.

Procedures: Isolated cardiac cells and tissue of rats are studied by using time-of-flight secondary ion mass spectrometry. This technique provides chemical composition of cardiac cell membrane and tissue surface in native form.

Results: The result is a spatially resolved chemical imaging of cell and tissue surfaces as a lateral distribution of biologically relevant molecules-phospholipids, along with fatty acids, and cholesterol. Phospholipids are represented by phosphatidylcholine and cardiolipin molecules and their fragments. Phosphatidylcholine polar head group at mass of 184.1 u has an origin in the cell membrane, and a two-dimensional distribution of this fragment provides clear chemical contours of the cell. The high-resolution contrast of the cell is observed within its environment represented with Na(+) ions. Images of PO(4)H(-) fragment and fatty acids with 16 or 18 C atoms are determined in cardiac tissue. Distributions of these 16 and 18 C fatty acids are the same within their groups, and interestingly, these two distribution groups are spatially complementary. Contours of phosphatidylcholine and cardiolipin fragments are also complementary, the distributions of 16 C fatty acids and phosphatidylcholine are identical, and the distributions of 18 C fatty acids and cardiolipin are also the same. This complementarity thus supports the chemical compositions of phosphatidylcholine and cardiolipin based on 16 C and 18 C fatty acids, respectively.

Conclusion: The method provides information not only about cell and tissue morphology, shape, and condition but also about cellular membrane chemical composition and lateral distribution of biologically relevant molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Membranes
  • Myocardium / cytology*
  • Myocardium / metabolism*
  • Principal Component Analysis
  • Rats
  • Rats, Wistar
  • Spectrometry, Mass, Secondary Ion / methods*