Cellular change and callose accumulation in zygotic embryos of Eleutherococcus senticosus caused by plasmolyzing pretreatment result in high frequency of single-cell-derived somatic embryogenesis
Eleutherococcus senticosus zygotic embryos were pretreated with 1.0 M mannitol or sucrose for 3-24 h. This pretreatment resulted in a high frequency of somatic-embryo formation on hormone-free medium. All the somatic embryos developed directly and independently from single epidermal cells on the sur...
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description | Eleutherococcus senticosus zygotic embryos were pretreated with 1.0 M mannitol or sucrose for 3-24 h. This pretreatment resulted in a high frequency of somatic-embryo formation on hormone-free medium. All the somatic embryos developed directly and independently from single epidermal cells on the surface of zygotic embryos after plasmolyzing pretreatment. Scanning electron microscopic observation revealed that the epidermal cells of hypocotyls rapidly became irregular and showed a random orientation before somatic-embryo development commenced. At the same time, the epidermal cells in the untreated control remained regular. Callose concentration determined by fluorometric analysis increased sharply in E. senticosus zygotic embryos after plasmolyzing pretreatment but remained low in the untreated control. Aniline blue fluorescent staining of callose showed that the plasmolyzing pretreatment of zygotic embryos resulted in heavy accumulation of callose between the plasma membrane and cell walls. On the basis of these results, we suggest that plasmolyzing pretreatment of zygotic embryos induces the accumulation of callose, and the interruption of cell-to-cell communication imposed by this might stimulate the reprogramming of epidermal cells into embryogenically competent cells and finally induce somatic-embryo development from single cells. |
doi_str_mv | 10.1007/s00709-006-0149-3 |
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This pretreatment resulted in a high frequency of somatic-embryo formation on hormone-free medium. All the somatic embryos developed directly and independently from single epidermal cells on the surface of zygotic embryos after plasmolyzing pretreatment. Scanning electron microscopic observation revealed that the epidermal cells of hypocotyls rapidly became irregular and showed a random orientation before somatic-embryo development commenced. At the same time, the epidermal cells in the untreated control remained regular. Callose concentration determined by fluorometric analysis increased sharply in E. senticosus zygotic embryos after plasmolyzing pretreatment but remained low in the untreated control. Aniline blue fluorescent staining of callose showed that the plasmolyzing pretreatment of zygotic embryos resulted in heavy accumulation of callose between the plasma membrane and cell walls. On the basis of these results, we suggest that plasmolyzing pretreatment of zygotic embryos induces the accumulation of callose, and the interruption of cell-to-cell communication imposed by this might stimulate the reprogramming of epidermal cells into embryogenically competent cells and finally induce somatic-embryo development from single cells.</description><identifier>ISSN: 0033-183X</identifier><identifier>EISSN: 1615-6102</identifier><identifier>DOI: 10.1007/s00709-006-0149-3</identifier><identifier>PMID: 16736252</identifier><language>eng</language><publisher>Austria: Springer Nature B.V</publisher><subject>Aniline ; Cell interactions ; Cell walls ; Cells ; Eleutherococcus - embryology ; Eleutherococcus - metabolism ; Eleutherococcus senticosus ; Embryonic Development ; Embryos ; Glucans - metabolism ; Hypocotyl - cytology ; Hypocotyl - drug effects ; Hypocotyl - ultrastructure ; Hypocotyls ; Mannitol ; Mannitol - pharmacology ; Plant Epidermis - ultrastructure ; Scanning electron microscopy ; Seeds - cytology ; Seeds - drug effects ; Seeds - metabolism ; Somatic embryogenesis ; Sucrose ; Sucrose - pharmacology ; Wound healing</subject><ispartof>Protoplasma, 2006-05, Vol.227 (2-4), p.105-112</ispartof><rights>Springer-Verlag 2006</rights><rights>Springer-Verlag 2006.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-fd430786aaa7a92856e162b189704d5c1750c8dcdd0e05df3c8e3185a57810183</citedby><cites>FETCH-LOGICAL-c379t-fd430786aaa7a92856e162b189704d5c1750c8dcdd0e05df3c8e3185a57810183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16736252$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>You, X.L</creatorcontrib><creatorcontrib>Yi, J.S</creatorcontrib><creatorcontrib>Choi, Y.E</creatorcontrib><title>Cellular change and callose accumulation in zygotic embryos of Eleutherococcus senticosus caused by plasmolyzing pretreatment result in high frequency of single-cell-derived somatic embryogenesis</title><title>Protoplasma</title><addtitle>Protoplasma</addtitle><description>Eleutherococcus senticosus zygotic embryos were pretreated with 1.0 M mannitol or sucrose for 3-24 h. This pretreatment resulted in a high frequency of somatic-embryo formation on hormone-free medium. All the somatic embryos developed directly and independently from single epidermal cells on the surface of zygotic embryos after plasmolyzing pretreatment. Scanning electron microscopic observation revealed that the epidermal cells of hypocotyls rapidly became irregular and showed a random orientation before somatic-embryo development commenced. At the same time, the epidermal cells in the untreated control remained regular. Callose concentration determined by fluorometric analysis increased sharply in E. senticosus zygotic embryos after plasmolyzing pretreatment but remained low in the untreated control. Aniline blue fluorescent staining of callose showed that the plasmolyzing pretreatment of zygotic embryos resulted in heavy accumulation of callose between the plasma membrane and cell walls. On the basis of these results, we suggest that plasmolyzing pretreatment of zygotic embryos induces the accumulation of callose, and the interruption of cell-to-cell communication imposed by this might stimulate the reprogramming of epidermal cells into embryogenically competent cells and finally induce somatic-embryo development from single cells.</description><subject>Aniline</subject><subject>Cell interactions</subject><subject>Cell walls</subject><subject>Cells</subject><subject>Eleutherococcus - embryology</subject><subject>Eleutherococcus - metabolism</subject><subject>Eleutherococcus senticosus</subject><subject>Embryonic Development</subject><subject>Embryos</subject><subject>Glucans - metabolism</subject><subject>Hypocotyl - cytology</subject><subject>Hypocotyl - drug effects</subject><subject>Hypocotyl - ultrastructure</subject><subject>Hypocotyls</subject><subject>Mannitol</subject><subject>Mannitol - pharmacology</subject><subject>Plant Epidermis - ultrastructure</subject><subject>Scanning electron microscopy</subject><subject>Seeds - cytology</subject><subject>Seeds - drug effects</subject><subject>Seeds - metabolism</subject><subject>Somatic embryogenesis</subject><subject>Sucrose</subject><subject>Sucrose - pharmacology</subject><subject>Wound healing</subject><issn>0033-183X</issn><issn>1615-6102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9ksGKFDEQhhtR3NnVB_CiAcFbayWZpNNHGVZXWPCgC95CJl3d00u6M6a6F3pfzxczzQwsePBSVZCvfn5Sf1G84fCRA1SfKBeoSwBdAt_WpXxWbLjmqtQcxPNiAyBlyY38dVFcEt0DgBKgXhYXXFdSCyU2xZ8dhjAHl5g_uLFD5saGeRdCpDx7Pw_5cerjyPqRPS5dnHrPcNinJRKLLbsOOE8HTNHHDBMjHDMRKY_ezYQN2y_sGBwNMSyP_dixY8IpoZuGTLKENIdp1T703YG1CX_POPpllaZMByx9Nlg2mPqHLEZxcE8OOhyRenpVvGhdIHx97lfF3Zfrn7ub8vb712-7z7ell1U9lW2zlVAZ7ZyrXC2M0si12HNTV7BtlOeVAm8a3zSAoJpWeoOSG-VUZTjkb7wqPpx0jylmmzTZoafVnhsxzmS1ASFMBRl8_w94H-c0Zm9WaL0VwLmu_0dxqJVWOtdM8RPlUyRK2Npj6geXlgzZNQX2lAKbU2DXFFiZd96elef9gM3TxvnsGXh3AloXretST_buR7YlgYPhxgj5F_bTuuE</recordid><startdate>20060501</startdate><enddate>20060501</enddate><creator>You, X.L</creator><creator>Yi, J.S</creator><creator>Choi, Y.E</creator><general>Springer Nature B.V</general><scope>FBQ</scope><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>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</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>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20060501</creationdate><title>Cellular change and callose accumulation in zygotic embryos of Eleutherococcus senticosus caused by plasmolyzing pretreatment result in high frequency of single-cell-derived somatic embryogenesis</title><author>You, X.L ; Yi, J.S ; Choi, Y.E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-fd430786aaa7a92856e162b189704d5c1750c8dcdd0e05df3c8e3185a57810183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aniline</topic><topic>Cell interactions</topic><topic>Cell walls</topic><topic>Cells</topic><topic>Eleutherococcus - embryology</topic><topic>Eleutherococcus - metabolism</topic><topic>Eleutherococcus senticosus</topic><topic>Embryonic Development</topic><topic>Embryos</topic><topic>Glucans - metabolism</topic><topic>Hypocotyl - cytology</topic><topic>Hypocotyl - drug effects</topic><topic>Hypocotyl - ultrastructure</topic><topic>Hypocotyls</topic><topic>Mannitol</topic><topic>Mannitol - pharmacology</topic><topic>Plant Epidermis - ultrastructure</topic><topic>Scanning electron microscopy</topic><topic>Seeds - cytology</topic><topic>Seeds - drug effects</topic><topic>Seeds - metabolism</topic><topic>Somatic embryogenesis</topic><topic>Sucrose</topic><topic>Sucrose - pharmacology</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>You, X.L</creatorcontrib><creatorcontrib>Yi, J.S</creatorcontrib><creatorcontrib>Choi, Y.E</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Protoplasma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>You, X.L</au><au>Yi, J.S</au><au>Choi, Y.E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular change and callose accumulation in zygotic embryos of Eleutherococcus senticosus caused by plasmolyzing pretreatment result in high frequency of single-cell-derived somatic embryogenesis</atitle><jtitle>Protoplasma</jtitle><addtitle>Protoplasma</addtitle><date>2006-05-01</date><risdate>2006</risdate><volume>227</volume><issue>2-4</issue><spage>105</spage><epage>112</epage><pages>105-112</pages><issn>0033-183X</issn><eissn>1615-6102</eissn><abstract>Eleutherococcus senticosus zygotic embryos were pretreated with 1.0 M mannitol or sucrose for 3-24 h. This pretreatment resulted in a high frequency of somatic-embryo formation on hormone-free medium. All the somatic embryos developed directly and independently from single epidermal cells on the surface of zygotic embryos after plasmolyzing pretreatment. Scanning electron microscopic observation revealed that the epidermal cells of hypocotyls rapidly became irregular and showed a random orientation before somatic-embryo development commenced. At the same time, the epidermal cells in the untreated control remained regular. Callose concentration determined by fluorometric analysis increased sharply in E. senticosus zygotic embryos after plasmolyzing pretreatment but remained low in the untreated control. Aniline blue fluorescent staining of callose showed that the plasmolyzing pretreatment of zygotic embryos resulted in heavy accumulation of callose between the plasma membrane and cell walls. On the basis of these results, we suggest that plasmolyzing pretreatment of zygotic embryos induces the accumulation of callose, and the interruption of cell-to-cell communication imposed by this might stimulate the reprogramming of epidermal cells into embryogenically competent cells and finally induce somatic-embryo development from single cells.</abstract><cop>Austria</cop><pub>Springer Nature B.V</pub><pmid>16736252</pmid><doi>10.1007/s00709-006-0149-3</doi><tpages>8</tpages></addata></record> |
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subjects | Aniline Cell interactions Cell walls Cells Eleutherococcus - embryology Eleutherococcus - metabolism Eleutherococcus senticosus Embryonic Development Embryos Glucans - metabolism Hypocotyl - cytology Hypocotyl - drug effects Hypocotyl - ultrastructure Hypocotyls Mannitol Mannitol - pharmacology Plant Epidermis - ultrastructure Scanning electron microscopy Seeds - cytology Seeds - drug effects Seeds - metabolism Somatic embryogenesis Sucrose Sucrose - pharmacology Wound healing |
title | Cellular change and callose accumulation in zygotic embryos of Eleutherococcus senticosus caused by plasmolyzing pretreatment result in high frequency of single-cell-derived somatic embryogenesis |
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