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Novel Soft Alginate Hydrogel Strongly Supports Neurite Growth and Protects Neurons Against Oxidative Stress
Neural tissue engineering focuses on development of biomaterials that could support regeneration of neurons after trauma as well as injury caused by degenerative diseases. In this work we describe novel soft alginate hydrogels, which provide an adhesive matrix for rat and human neurons and facilitat...
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Published in: | Tissue engineering. Part A 2012-01, Vol.18 (1-2), p.55-66 |
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container_title | Tissue engineering. Part A |
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creator | Matyash, Marina Despang, Florian Mandal, Rakesh Fiore, Diccon Gelinsky, Michael Ikonomidou, Chrysanthy |
description | Neural tissue engineering focuses on development of biomaterials that could support regeneration of neurons after trauma as well as injury caused by degenerative diseases. In this work we describe novel soft alginate hydrogels, which provide an adhesive matrix for rat and human neurons and facilitate neurite outgrowth. Only soft hydrogels, prepared with sub-stoichiometric concentrations of Ca
2+
, Ba
2+
, and Sr
2+
cations by cross-linking with no >10% of all potentially available gelation sites in alginate, facilitated rapid and abundant neurite outgrowth in primary neuronal monolayer cultures, neural spheroids, and neurons derived from rat and human neural stem cells. To support neurite growth, hydrogels did not require modification by any extracellular matrix components and were prepared from high as well as low viscous alginates of different origin. In addition, neurons cultured on soft hydrogels were resistant to oxidative stress injury induced by hydrogen peroxide. These findings, which apply both to rat and human neurons, go beyond the well-described role of alginates as inert materials for cell encapsulation. Such soft alginate hydrogels may be useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders, for promoting neuronal regeneration in the peripheral and central nervous system and for neural tissue engineering applications. |
doi_str_mv | 10.1089/ten.tea.2011.0097 |
format | article |
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2+
, Ba
2+
, and Sr
2+
cations by cross-linking with no >10% of all potentially available gelation sites in alginate, facilitated rapid and abundant neurite outgrowth in primary neuronal monolayer cultures, neural spheroids, and neurons derived from rat and human neural stem cells. To support neurite growth, hydrogels did not require modification by any extracellular matrix components and were prepared from high as well as low viscous alginates of different origin. In addition, neurons cultured on soft hydrogels were resistant to oxidative stress injury induced by hydrogen peroxide. These findings, which apply both to rat and human neurons, go beyond the well-described role of alginates as inert materials for cell encapsulation. Such soft alginate hydrogels may be useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders, for promoting neuronal regeneration in the peripheral and central nervous system and for neural tissue engineering applications.</description><identifier>ISSN: 1937-3341</identifier><identifier>EISSN: 1937-335X</identifier><identifier>DOI: 10.1089/ten.tea.2011.0097</identifier><identifier>PMID: 21770866</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Alginates - pharmacology ; Animals ; Barium - pharmacology ; Biomedical materials ; Calcium - pharmacology ; Cell growth ; Cell Survival - drug effects ; Cross-Linking Reagents - pharmacology ; Cytoprotection - drug effects ; Glucuronic Acid - pharmacology ; Hexuronic Acids - pharmacology ; Hydrogel, Polyethylene Glycol Dimethacrylate - pharmacology ; Hydrogels ; Hydrogen Peroxide - pharmacology ; Microscopy, Fluorescence ; Neurites - drug effects ; Neurites - metabolism ; Neurons ; Original Articles ; Oxidative stress ; Oxidative Stress - drug effects ; Rats ; Rats, Wistar ; Spheroids, Cellular - cytology ; Spheroids, Cellular - drug effects ; Strontium - pharmacology ; Tissue engineering</subject><ispartof>Tissue engineering. Part A, 2012-01, Vol.18 (1-2), p.55-66</ispartof><rights>2012, Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2012, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-9e36c0cc5778ee9d326be8d39c5fc322dd9ef0c36592015ddf1253c7d1d0a72b3</citedby><cites>FETCH-LOGICAL-c455t-9e36c0cc5778ee9d326be8d39c5fc322dd9ef0c36592015ddf1253c7d1d0a72b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.liebertpub.com/doi/epdf/10.1089/ten.tea.2011.0097$$EPDF$$P50$$Gmaryannliebert$$H</linktopdf><linktohtml>$$Uhttps://www.liebertpub.com/doi/full/10.1089/ten.tea.2011.0097$$EHTML$$P50$$Gmaryannliebert$$H</linktohtml><link.rule.ids>314,776,780,3029,21702,27901,27902,55266,55278</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21770866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matyash, Marina</creatorcontrib><creatorcontrib>Despang, Florian</creatorcontrib><creatorcontrib>Mandal, Rakesh</creatorcontrib><creatorcontrib>Fiore, Diccon</creatorcontrib><creatorcontrib>Gelinsky, Michael</creatorcontrib><creatorcontrib>Ikonomidou, Chrysanthy</creatorcontrib><title>Novel Soft Alginate Hydrogel Strongly Supports Neurite Growth and Protects Neurons Against Oxidative Stress</title><title>Tissue engineering. Part A</title><addtitle>Tissue Eng Part A</addtitle><description>Neural tissue engineering focuses on development of biomaterials that could support regeneration of neurons after trauma as well as injury caused by degenerative diseases. In this work we describe novel soft alginate hydrogels, which provide an adhesive matrix for rat and human neurons and facilitate neurite outgrowth. Only soft hydrogels, prepared with sub-stoichiometric concentrations of Ca
2+
, Ba
2+
, and Sr
2+
cations by cross-linking with no >10% of all potentially available gelation sites in alginate, facilitated rapid and abundant neurite outgrowth in primary neuronal monolayer cultures, neural spheroids, and neurons derived from rat and human neural stem cells. To support neurite growth, hydrogels did not require modification by any extracellular matrix components and were prepared from high as well as low viscous alginates of different origin. In addition, neurons cultured on soft hydrogels were resistant to oxidative stress injury induced by hydrogen peroxide. These findings, which apply both to rat and human neurons, go beyond the well-described role of alginates as inert materials for cell encapsulation. Such soft alginate hydrogels may be useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders, for promoting neuronal regeneration in the peripheral and central nervous system and for neural tissue engineering applications.</description><subject>Alginates - pharmacology</subject><subject>Animals</subject><subject>Barium - pharmacology</subject><subject>Biomedical materials</subject><subject>Calcium - pharmacology</subject><subject>Cell growth</subject><subject>Cell Survival - drug effects</subject><subject>Cross-Linking Reagents - pharmacology</subject><subject>Cytoprotection - drug effects</subject><subject>Glucuronic Acid - pharmacology</subject><subject>Hexuronic Acids - pharmacology</subject><subject>Hydrogel, Polyethylene Glycol Dimethacrylate - pharmacology</subject><subject>Hydrogels</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Microscopy, Fluorescence</subject><subject>Neurites - drug effects</subject><subject>Neurites - metabolism</subject><subject>Neurons</subject><subject>Original Articles</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Spheroids, Cellular - cytology</subject><subject>Spheroids, Cellular - drug effects</subject><subject>Strontium - pharmacology</subject><subject>Tissue engineering</subject><issn>1937-3341</issn><issn>1937-335X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkU1LJDEQhoMofq0_wIsEL3uaMR-TpHMcxNUFUUGFvTWZpHps7UnGJO3u_HvTzKwHL3ooUlSeeqB4ETqmZExJpc8y-HEGM2aE0jEhWm2hfaq5GnEu_mx_9BO6hw5SeiZEEqnULtpjVClSSbmPXm7CG3T4PjQZT7t5600GfLVyMcyHcY7Bz7sVvu-XyxBzwjfQx7YglzH8zU_YeIfvYshgN3_BJzydm9anjG__tc7k9g0GD6T0A-00pktwtHkP0eOvi4fzq9H17eXv8-n1yE6EyCMNXFpirVCqAtCOMzmDynFtRWM5Y85paIjlUuhyuHCuoUxwqxx1xCg244fo59q7jOG1h5TrRZssdJ3xEPpUa8YZIUKSr0k6kVIJXhXy9BP5HProyxkF4hOlFR10dA3ZGFKK0NTL2C5MXNWU1ENidUmslKmHxOohsbJzshH3swW4j43_ERVArYFhbLzvWphBzN9QvwOuSabl</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Matyash, Marina</creator><creator>Despang, Florian</creator><creator>Mandal, Rakesh</creator><creator>Fiore, Diccon</creator><creator>Gelinsky, Michael</creator><creator>Ikonomidou, Chrysanthy</creator><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20120101</creationdate><title>Novel Soft Alginate Hydrogel Strongly Supports Neurite Growth and Protects Neurons Against Oxidative Stress</title><author>Matyash, Marina ; 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Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matyash, Marina</au><au>Despang, Florian</au><au>Mandal, Rakesh</au><au>Fiore, Diccon</au><au>Gelinsky, Michael</au><au>Ikonomidou, Chrysanthy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Soft Alginate Hydrogel Strongly Supports Neurite Growth and Protects Neurons Against Oxidative Stress</atitle><jtitle>Tissue engineering. Part A</jtitle><addtitle>Tissue Eng Part A</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>18</volume><issue>1-2</issue><spage>55</spage><epage>66</epage><pages>55-66</pages><issn>1937-3341</issn><eissn>1937-335X</eissn><abstract>Neural tissue engineering focuses on development of biomaterials that could support regeneration of neurons after trauma as well as injury caused by degenerative diseases. In this work we describe novel soft alginate hydrogels, which provide an adhesive matrix for rat and human neurons and facilitate neurite outgrowth. Only soft hydrogels, prepared with sub-stoichiometric concentrations of Ca
2+
, Ba
2+
, and Sr
2+
cations by cross-linking with no >10% of all potentially available gelation sites in alginate, facilitated rapid and abundant neurite outgrowth in primary neuronal monolayer cultures, neural spheroids, and neurons derived from rat and human neural stem cells. To support neurite growth, hydrogels did not require modification by any extracellular matrix components and were prepared from high as well as low viscous alginates of different origin. In addition, neurons cultured on soft hydrogels were resistant to oxidative stress injury induced by hydrogen peroxide. These findings, which apply both to rat and human neurons, go beyond the well-described role of alginates as inert materials for cell encapsulation. Such soft alginate hydrogels may be useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders, for promoting neuronal regeneration in the peripheral and central nervous system and for neural tissue engineering applications.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>21770866</pmid><doi>10.1089/ten.tea.2011.0097</doi><tpages>12</tpages></addata></record> |
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subjects | Alginates - pharmacology Animals Barium - pharmacology Biomedical materials Calcium - pharmacology Cell growth Cell Survival - drug effects Cross-Linking Reagents - pharmacology Cytoprotection - drug effects Glucuronic Acid - pharmacology Hexuronic Acids - pharmacology Hydrogel, Polyethylene Glycol Dimethacrylate - pharmacology Hydrogels Hydrogen Peroxide - pharmacology Microscopy, Fluorescence Neurites - drug effects Neurites - metabolism Neurons Original Articles Oxidative stress Oxidative Stress - drug effects Rats Rats, Wistar Spheroids, Cellular - cytology Spheroids, Cellular - drug effects Strontium - pharmacology Tissue engineering |
title | Novel Soft Alginate Hydrogel Strongly Supports Neurite Growth and Protects Neurons Against Oxidative Stress |
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