Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii

Membrane microdomains or rafts, sterol- and sphingolipid-rich microdomains in the plasma membrane have been studied extensively in mammalian cells. Recently, rafts were found to mediate virulence in a variety of parasites, including Toxoplasma gondii. However, it has been difficult to examine a two-...

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Main Authors: Rikako Konishi, Yuna Kurokawa, Kanna Tomioku, Tatsunori Masatani, Xuenan Xuan, Akikazu Fujita
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:European Journal of Cell Biology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0171933520300881
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spelling doaj-ab9afe7d2a8d49b9b3fdd8a4b708eff62021-04-16T04:48:07ZengElsevierEuropean Journal of Cell Biology0171-93352021-03-011002151149Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondiiRikako Konishi0Yuna Kurokawa1Kanna Tomioku2Tatsunori Masatani3Xuenan Xuan4Akikazu Fujita5Department of Molecular and Cell Biology and Biochemistry, Basic Veterinary Science, Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima, 890-0065, JapanDepartment of Molecular and Cell Biology and Biochemistry, Basic Veterinary Science, Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima, 890-0065, JapanDepartment of Molecular and Cell Biology and Biochemistry, Basic Veterinary Science, Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima, 890-0065, JapanTransboundary Animal Diseases Research Center, Joint Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima, 890-0065, JapanNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, 080-8555, JapanDepartment of Molecular and Cell Biology and Biochemistry, Basic Veterinary Science, Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima, 890-0065, Japan; Corresponding author at: Department of Molecular and Cell Biology and Biochemistry, Basic Veterinary Science, Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima, 890-0065, Japan.Membrane microdomains or rafts, sterol- and sphingolipid-rich microdomains in the plasma membrane have been studied extensively in mammalian cells. Recently, rafts were found to mediate virulence in a variety of parasites, including Toxoplasma gondii. However, it has been difficult to examine a two-dimensional distribution of lipid molecules at a nanometer scale. We tried to determine the distribution of glycosphingolipids GM1 and GM3, putative raft components in the T. gondii cell membrane in this study, using a rapid-frozen and freeze-fractured immuno-electron microscopy method. This method physically stabilized molecules in situ, to minimize the probability of artefactual disruption. Labeling of GM3, but not GM1, was observed in the exoplasmic (or luminal), but not the cytoplasmic, leaflet of the inner membrane complex (IMC) in T. gondii infected in human foreskin fibroblast-1 (HFF-1). No labeling was detected in any leaflet of the T. gondii plasma membrane. In contrast to HFF-1, T. gondii infected in mouse fibroblast (MF), labelings of both GM1 and GM3 were detected in the IMC luminal leaflet, although GM1′s gold labeling density was very low. The same freeze-fracture EM method showed that both GM1 and GM3 were expressed in the exoplasmic leaflet of the MF plasma membrane. However, labeling of only GM3, but not GM1, was detected in the exoplasmic leaflet of the HFF-1 plasma membrane. These results suggest that GM1 or GM3, localized in the IMC, is obtained from the plasma membranes of infected host mammalian cells. Furthermore, the localization of microdomains or rafts in the luminal leaflets of the intracellular confined space IMC organelle of T. gondii suggests a novel characteristic of rafts.http://www.sciencedirect.com/science/article/pii/S0171933520300881MicrodomainLipidFreeze–fractureElectron microscopyNanometer scale
collection DOAJ
language English
format Article
sources DOAJ
author Rikako Konishi
Yuna Kurokawa
Kanna Tomioku
Tatsunori Masatani
Xuenan Xuan
Akikazu Fujita
spellingShingle Rikako Konishi
Yuna Kurokawa
Kanna Tomioku
Tatsunori Masatani
Xuenan Xuan
Akikazu Fujita
Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii
European Journal of Cell Biology
Microdomain
Lipid
Freeze–fracture
Electron microscopy
Nanometer scale
author_facet Rikako Konishi
Yuna Kurokawa
Kanna Tomioku
Tatsunori Masatani
Xuenan Xuan
Akikazu Fujita
author_sort Rikako Konishi
title Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii
title_short Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii
title_full Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii
title_fullStr Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii
title_full_unstemmed Raft microdomain localized in the luminal leaflet of inner membrane complex of living Toxoplasma gondii
title_sort raft microdomain localized in the luminal leaflet of inner membrane complex of living toxoplasma gondii
publisher Elsevier
series European Journal of Cell Biology
issn 0171-9335
publishDate 2021-03-01
description Membrane microdomains or rafts, sterol- and sphingolipid-rich microdomains in the plasma membrane have been studied extensively in mammalian cells. Recently, rafts were found to mediate virulence in a variety of parasites, including Toxoplasma gondii. However, it has been difficult to examine a two-dimensional distribution of lipid molecules at a nanometer scale. We tried to determine the distribution of glycosphingolipids GM1 and GM3, putative raft components in the T. gondii cell membrane in this study, using a rapid-frozen and freeze-fractured immuno-electron microscopy method. This method physically stabilized molecules in situ, to minimize the probability of artefactual disruption. Labeling of GM3, but not GM1, was observed in the exoplasmic (or luminal), but not the cytoplasmic, leaflet of the inner membrane complex (IMC) in T. gondii infected in human foreskin fibroblast-1 (HFF-1). No labeling was detected in any leaflet of the T. gondii plasma membrane. In contrast to HFF-1, T. gondii infected in mouse fibroblast (MF), labelings of both GM1 and GM3 were detected in the IMC luminal leaflet, although GM1′s gold labeling density was very low. The same freeze-fracture EM method showed that both GM1 and GM3 were expressed in the exoplasmic leaflet of the MF plasma membrane. However, labeling of only GM3, but not GM1, was detected in the exoplasmic leaflet of the HFF-1 plasma membrane. These results suggest that GM1 or GM3, localized in the IMC, is obtained from the plasma membranes of infected host mammalian cells. Furthermore, the localization of microdomains or rafts in the luminal leaflets of the intracellular confined space IMC organelle of T. gondii suggests a novel characteristic of rafts.
topic Microdomain
Lipid
Freeze–fracture
Electron microscopy
Nanometer scale
url http://www.sciencedirect.com/science/article/pii/S0171933520300881
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