Transport and uptake effects of marine complex lipid liposomes in small intestinal epithelial cell models

Nowadays, marine complex lipids, including starfish phospholipids (SFP) and cerebrosides (SFC) separated from Asterias amurensis as well as sea cucumber phospholipids (SCP) and cerebrosides (SCC) isolated from Cucumaria frondosa , have received much attention because of their potent biological activ...

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Veröffentlicht in:Food & function 2016-04, Vol.7 (4), p.194-1914
Hauptverfasser: Du, Lei, Yang, Yu-Hong, Xu, Jie, Wang, Yu-Ming, Xue, Chang-Hu, Kurihara, Hideyuki, Takahashi, Koretaro
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container_end_page 1914
container_issue 4
container_start_page 194
container_title Food & function
container_volume 7
creator Du, Lei
Yang, Yu-Hong
Xu, Jie
Wang, Yu-Ming
Xue, Chang-Hu
Kurihara, Hideyuki
Takahashi, Koretaro
description Nowadays, marine complex lipids, including starfish phospholipids (SFP) and cerebrosides (SFC) separated from Asterias amurensis as well as sea cucumber phospholipids (SCP) and cerebrosides (SCC) isolated from Cucumaria frondosa , have received much attention because of their potent biological activities. However, little information is known on the transport and uptake of these lipids in liposome forms in small intestinal cells. Therefore, this study was undertaken to investigate the effects of these complex lipid liposomes on transport and uptake in Caco-2 and M cell monolayer models. The results revealed that SFP and SCP contained 42% and 47.9% eicosapentaenoic acid (EPA), respectively. The average particle sizes of liposomes prepared in this study were from 169 to 189 nm. We found that the transport of the liposomes across the M cell monolayer model was much higher than the Caco-2 cell monolayer model. The liposomes consisting of SFP or SCP showed significantly higher transport and uptake than soy phospholipid (soy-PL) liposomes in both Caco-2 and M cell monolayer models. Our results also exhibited that treatment with 1 mM liposomes composed of SFP or SCP for 3 h tended to increase the EPA content in phospholipid fractions of both differentiated Caco-2 and M cells. Moreover, it was also found that the hybrid liposomes consisting of SFP/SFC/cholesterol (Chol) revealed higher transport and uptake across the M cell monolayer in comparison with other liposomes. Furthermore, treatment with SFP/SFC/Chol liposomes could notably decrease the trans-epithelial electrical resistance (TEER) values of Caco-2 and M cell monolayers. The present data also showed that the cell viability of differentiated Caco-2 and M cells was not affected after the treatment with marine complex lipids or soy-PL liposomes. Based on the data in this study, it was suggested that marine complex lipid liposomes exhibit prominent transport and uptake in small intestinal epithelial cell models. Transport and uptake effects of marine complex lipid liposomes in Caco-2 and M cell monolayer models.
doi_str_mv 10.1039/c6fo00066e
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However, little information is known on the transport and uptake of these lipids in liposome forms in small intestinal cells. Therefore, this study was undertaken to investigate the effects of these complex lipid liposomes on transport and uptake in Caco-2 and M cell monolayer models. The results revealed that SFP and SCP contained 42% and 47.9% eicosapentaenoic acid (EPA), respectively. The average particle sizes of liposomes prepared in this study were from 169 to 189 nm. We found that the transport of the liposomes across the M cell monolayer model was much higher than the Caco-2 cell monolayer model. The liposomes consisting of SFP or SCP showed significantly higher transport and uptake than soy phospholipid (soy-PL) liposomes in both Caco-2 and M cell monolayer models. Our results also exhibited that treatment with 1 mM liposomes composed of SFP or SCP for 3 h tended to increase the EPA content in phospholipid fractions of both differentiated Caco-2 and M cells. Moreover, it was also found that the hybrid liposomes consisting of SFP/SFC/cholesterol (Chol) revealed higher transport and uptake across the M cell monolayer in comparison with other liposomes. Furthermore, treatment with SFP/SFC/Chol liposomes could notably decrease the trans-epithelial electrical resistance (TEER) values of Caco-2 and M cell monolayers. The present data also showed that the cell viability of differentiated Caco-2 and M cells was not affected after the treatment with marine complex lipids or soy-PL liposomes. Based on the data in this study, it was suggested that marine complex lipid liposomes exhibit prominent transport and uptake in small intestinal epithelial cell models. 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Yang, Yu-Hong ; Xu, Jie ; Wang, Yu-Ming ; Xue, Chang-Hu ; Kurihara, Hideyuki ; Takahashi, Koretaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-3936433bf5cb9145431f56e917d68a9d6717fee8fa9833855bf776985e5d073c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Asterias</topic><topic>Asterias - chemistry</topic><topic>Asteroidea</topic><topic>Biological Transport</topic><topic>Caco-2 Cells</topic><topic>Cell Survival</topic><topic>Cerebrosides - chemistry</topic><topic>Cerebrosides - metabolism</topic><topic>Cucumaria - chemistry</topic><topic>Cucumaria frondosa</topic><topic>Epithelial Cells - metabolism</topic><topic>Holothurioidea</topic><topic>Humans</topic><topic>Intestine, Small - metabolism</topic><topic>Liposomes - chemistry</topic><topic>Liposomes - metabolism</topic><topic>Marine</topic><topic>Models, Biological</topic><topic>Phospholipids - chemistry</topic><topic>Phospholipids - metabolism</topic><topic>Seafood - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Du, Lei</creatorcontrib><creatorcontrib>Yang, Yu-Hong</creatorcontrib><creatorcontrib>Xu, Jie</creatorcontrib><creatorcontrib>Wang, Yu-Ming</creatorcontrib><creatorcontrib>Xue, Chang-Hu</creatorcontrib><creatorcontrib>Kurihara, Hideyuki</creatorcontrib><creatorcontrib>Takahashi, Koretaro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science &amp; 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Moreover, it was also found that the hybrid liposomes consisting of SFP/SFC/cholesterol (Chol) revealed higher transport and uptake across the M cell monolayer in comparison with other liposomes. Furthermore, treatment with SFP/SFC/Chol liposomes could notably decrease the trans-epithelial electrical resistance (TEER) values of Caco-2 and M cell monolayers. The present data also showed that the cell viability of differentiated Caco-2 and M cells was not affected after the treatment with marine complex lipids or soy-PL liposomes. Based on the data in this study, it was suggested that marine complex lipid liposomes exhibit prominent transport and uptake in small intestinal epithelial cell models. Transport and uptake effects of marine complex lipid liposomes in Caco-2 and M cell monolayer models.</abstract><cop>England</cop><pmid>27001385</pmid><doi>10.1039/c6fo00066e</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Animals
Asterias
Asterias - chemistry
Asteroidea
Biological Transport
Caco-2 Cells
Cell Survival
Cerebrosides - chemistry
Cerebrosides - metabolism
Cucumaria - chemistry
Cucumaria frondosa
Epithelial Cells - metabolism
Holothurioidea
Humans
Intestine, Small - metabolism
Liposomes - chemistry
Liposomes - metabolism
Marine
Models, Biological
Phospholipids - chemistry
Phospholipids - metabolism
Seafood - analysis
title Transport and uptake effects of marine complex lipid liposomes in small intestinal epithelial cell models
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