| Literature DB >> 31204806 |
Emi Takeo1, Yuki Sugiura2, Tatsuki Uemura3, Koshiro Nishimoto2,4, Masanori Yasuda5, Eiji Sugiyama2, Sumio Ohtsuki3, Tatsuya Higashi6, Tetsuo Nishikawa7, Makoto Suematsu2, Eiichiro Fukusaki1, Shuichi Shimma1.
Abstract
Visualizing tissue distribution of steroid hormones is a promising application of MALDI mass spectrometry imaging (MSI). On-tissue chemical derivatization using Girard's T reagent has enhanced the ionization efficiency of steroids. However, discriminating between structural isomers with distinct bioactivities remains a challenge. Herein, we used ion trap MS/tandem MS (MS3) to distinguish a mineralcorticoid aldosterone (Aldo) and a glucocorticoid cortisol (F), from their structural isomers. Our method is also useful to detect hybrid steroids (18-hydroxycortisol [18-OHF] and 18-oxocortisol) with sufficient signal-to-noise ratio. The clinical applicability of the tandem MS method was evaluated by analyzing F, Aldo, and 18-OHF distributions in human adrenal glands. In such clinical specimens, small Aldo-producing cell clusters (APCCs) were identified and were first found to produce a high level of Aldo and not to contain F. Moreover, a part of APCCs produced 18-OHF, presumably converted from F by APCC-specific CYP11B2 activity. Catecholamine species were also visualized with another derivatization reagent (TAHS), and those profiling successfully discriminated pheochromocytoma species. These tandem MSI-methods, coupled with on-tissue chemical derivatization has proven to be useful for detecting low-abundance steroids, including Aldo and hybrid steroids and thus identifying steroid hormone-producing lesions.Entities:
Year: 2019 PMID: 31204806 DOI: 10.1021/acs.analchem.9b00619
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986