Literature DB >> 26915109

A2B5+/GFAP+ Cells of Rat Spinal Cord Share a Similar Lipid Profile with Progenitor Cells: A Comparative Lipidomic Study.

Yutaka Itokazu1,2,3,4, Nobuyoshi Tajima2,5, Laura Kerosuo2,6, Pentti Somerharju2, Hannu Sariola2, Robert K Yu3,4, Reijo Käkelä7,8.   

Abstract

The central nervous system (CNS) harbors multiple glial fibrillary acidic protein (GFAP) expressing cell types. In addition to the most abundant cell type of the CNS, the astrocytes, various stem cells and progenitor cells also contain GFAP+ populations. Here, in order to distinguish between two types of GFAP expressing cells with or without the expression of the A2B5 antigens, we performed lipidomic analyses on A2B5+/GFAP+ and A2B5-/GFAP+ cells from rat spinal cord. First, A2B5+/GFAP- progenitors were exposed to the leukemia inhibitory factor (LIF) or bone morphogenetic protein (BMP) to induce their differentiation to A2B5+/GFAP+ cells or A2B5-/GFAP+ astrocytes, respectively. The cells were then analyzed for changes in their phospholipid, sphingolipid or acyl chain profiles by mass spectrometry and gas chromatography. Compared to A2B5+/GFAP- progenitors, A2B5-/GFAP+ astrocytes contained higher amounts of ether phospholipids (especially the species containing arachidonic acid) and sphingomyelin, which may indicate characteristics of cellular differentiation and inability for multipotency. In comparison, principal component analyses revealed that the lipid composition of A2B5+/GFAP+ cells retained many of the characteristics of A2B5+/GFAP- progenitors, but their lipid profile was different from that of A2B5-/GFAP+ astrocytes. Thus, our study demonstrated that two GFAP+ cell populations have distinct lipid profiles with the A2B5+/GFAP+ cells sharing a phospholipid profile with progenitors rather than astrocytes. The progenitor cells may require regulated low levels of lipids known to mediate signaling functions in differentiated cells, and the precursor lipid profiles may serve as one measure of the differentiation capacity of a cell population.

Entities:  

Keywords:  A2B5 antigen; Astrocyte; Glial fibrillary acidic protein; Glial progenitor/precursor cell; Lipidomics; Mass spectrometry; Phospholipid; Sphingolipid

Mesh:

Substances:

Year:  2016        PMID: 26915109     DOI: 10.1007/s11064-016-1867-3

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  72 in total

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Authors:  Nobuyoshi Tajima; Yutaka Itokazu; Esa R Korpi; Pentti Somerharju; Reijo Käkelä
Journal:  J Biol Chem       Date:  2010-12-06       Impact factor: 5.157

Review 2.  It's a lipid's world: bioactive lipid metabolism and signaling in neural stem cell differentiation.

Authors:  Erhard Bieberich
Journal:  Neurochem Res       Date:  2012-01-14       Impact factor: 3.996

3.  The monoclonal antibody A2B5 is specific to ganglioside GQ1c.

Authors:  N Kasai; R K Yu
Journal:  Brain Res       Date:  1983-10-24       Impact factor: 3.252

4.  Long-term fate of neural precursor cells following transplantation into developing and adult CNS.

Authors:  A C Lepore; B Neuhuber; T M Connors; S S W Han; Y Liu; M P Daniels; M S Rao; I Fischer
Journal:  Neuroscience       Date:  2006-02-03       Impact factor: 3.590

5.  Quantitative analysis of biological membrane lipids at the low picomole level by nano-electrospray ionization tandem mass spectrometry.

Authors:  B Brügger; G Erben; R Sandhoff; F T Wieland; W D Lehmann
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-18       Impact factor: 11.205

6.  Amyloid β-peptide 1-42 modulates the proliferation of mouse neural stem cells: upregulation of fucosyltransferase IX and notch signaling.

Authors:  Yutaka Itokazu; Robert K Yu
Journal:  Mol Neurobiol       Date:  2014-01-17       Impact factor: 5.590

7.  Roles of lipid rafts in integrin-dependent adhesion and gp130 signalling pathway in mouse embryonic neural precursor cells.

Authors:  Makoto Yanagisawa; Kazuo Nakamura; Tetsuya Taga
Journal:  Genes Cells       Date:  2004-09       Impact factor: 1.891

8.  Developmental changes of glycosphingolipids and expression of glycogenes in mouse brains.

Authors:  Sathaporn Ngamukote; Makoto Yanagisawa; Toshio Ariga; Susumu Ando; Robert K Yu
Journal:  J Neurochem       Date:  2007-09-19       Impact factor: 5.372

Review 9.  The role of glycosphingolipid metabolism in the developing brain.

Authors:  Robert K Yu; Yoshihiko Nakatani; Makoto Yanagisawa
Journal:  J Lipid Res       Date:  2008-10-09       Impact factor: 5.922

10.  Human astrocytes derived from glial restricted progenitors support regeneration of the injured spinal cord.

Authors:  Christopher Haas; Itzhak Fischer
Journal:  J Neurotrauma       Date:  2013-06-12       Impact factor: 5.269

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  4 in total

1.  Metabolism and phospholipid assembly of polyunsaturated fatty acids in human bone marrow mesenchymal stromal cells.

Authors:  Feven Tigistu-Sahle; Milla Lampinen; Lotta Kilpinen; Minna Holopainen; Petri Lehenkari; Saara Laitinen; Reijo Käkelä
Journal:  J Lipid Res       Date:  2016-11-16       Impact factor: 5.922

Review 2.  Gangliosides in Nerve Cell Specification.

Authors:  Yutaka Itokazu; Jing Wang; Robert K Yu
Journal:  Prog Mol Biol Transl Sci       Date:  2018-01-17       Impact factor: 3.622

Review 3.  Lipid rafts and neurodegeneration: structural and functional roles in physiologic aging and neurodegenerative diseases.

Authors:  Sara Grassi; Paola Giussani; Laura Mauri; Simona Prioni; Sandro Sonnino; Alessandro Prinetti
Journal:  J Lipid Res       Date:  2019-12-23       Impact factor: 5.922

4.  Ganglioside Microdomains on Cellular and Intracellular Membranes Regulate Neuronal Cell Fate Determination.

Authors:  Yutaka Itokazu; Robert K Yu
Journal:  Adv Neurobiol       Date:  2023
  4 in total

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