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Glycolipids: Essential regulator of neuro-inflammation, metabolism and gliomagenesis.

Authors :
Furukawa K
Ohmi Y
Ji S
Zhang P
Bhuiyan RH
Ohkawa Y
Tajima O
Hashimoto N
Furukawa K
Source :
Biochimica et biophysica acta. General subjects [Biochim Biophys Acta Gen Subj] 2017 Oct; Vol. 1861 (10), pp. 2479-2484. Date of Electronic Publication: 2017 Jun 07.
Publication Year :
2017

Abstract

Gene knockout mice of glycosyltransferases have clearly showed roles of their products in the bodies, while there are examples where phenotype of knockout was much less severe than expected probably due to functional redundancy. The most striking novel finding obtained from ganglioside-deficient mice was that progressive inflammatory reaction took place, leading to neurodegeneration. In particular, dysfunction of complement-regulatory proteins due to deteriorated architecture of lipid rafts seemed to be essential mechanisms for the inflammation. Furthermore, roles of gangliosides in neurons were demonstrated by neuron-specific transgenic of B4galnt1 with genetic background of B4galnt1 deficiency. From study of gene knockout mice of St8sia1, new roles of b-series gangliosides in leptin secretion from adipocytes, and roles of a-series gangliosides in leptin receptor, ObR in hypothalamus were demonstrated, leading to apparent intact balance of energy. Essential roles of b-series gangliosides in malignant properties of gliomas were also shown, suggesting their roles in the regulation of inflammation and proliferation in nervous tissues. How to apply these findings for the control of newly discovered patients with ganglioside deficiency remains to be investigated. This article is part of a Special Issue entitled Neuro-glycoscience, edited by Kenji Kadomatsu and Hiroshi Kitagawa.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
0304-4165
Volume :
1861
Issue :
10
Database :
MEDLINE
Journal :
Biochimica et biophysica acta. General subjects
Publication Type :
Academic Journal
Accession number :
28602513
Full Text :
https://doi.org/10.1016/j.bbagen.2017.06.007