Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)

Detalhes bibliográficos
Autor(a) principal: Machado, Silvia Rodrigues [UNESP]
Data de Publicação: 2021
Outros Autores: Rodrigues, Tatiane Maria [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00425-021-03663-8
http://hdl.handle.net/11449/229075
Resumo: Main conclusion: The cytological changes underlying the formation of an apoplasmic barrier in the multi-layered extrafloral nectaries of Citharexylum myrianthum are compatible with the synthesis, transport and deposition of suberin. In terms of ontogenesis and function, the intermediate layers of these nectaries are homologous with the stalks of nectar-secreting trichomes. Abstract: Anticlinal cell wall impregnations are common in trichomatic nectaries and their functions as endodermis-like barriers have been discussed because of possible direct effects on the nectary physiology, mainly in the nectar secretion and resorption. However, the cytological events linked to nectary wall impregnations remain little explored. This study documents the ontogenesis and the fine structure of the EFN cells, and cytological events linked to the wall impregnations of multi-layered extrafloral nectaries (EFNs) in Citharexylum myrianthum Cham. (Verbenaceae). EFNs are patelliform, and differentiated into (a) a multicellular foot, which is compound in structure and vascularised with phloem strands, (b) a bi-layered intermediate region with thickened cell walls and (c) a single-layered secretory region with palisade-like cells. EFNs are protodermal in origin, starting with a single protodermal cell and ending with the complex, multi-layered structure. The cell wall impregnations first appear in the very young EFN and increase towards maturity. Lipid patches (assumed to be suberin) are deposited on the inner faces of the primary walls, first along the anticlinal walls and then extend to the periclinal walls. On both walls, plasmodesmata remain apparently intact during the maturation of the EFNs. In the peripheral cytoplasm there are abundant polymorphic plastids, well-developed Golgi bodies often close to rough endoplasmic reticulum profiles, mitochondria and polyribosomes. Cytological events linked to the wall impregnations are consistent with suberin synthesis, transport and deposition. Our findings offer new insights into the structure-properties of specialised nectary cell walls and so should contribute to our knowledge of the physiological and protective roles of this structure in nectar glands.
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spelling Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)Cell wall impregnationLipid barrierNectar secretionPatelliform extrafloral nectaryUltrastructureMain conclusion: The cytological changes underlying the formation of an apoplasmic barrier in the multi-layered extrafloral nectaries of Citharexylum myrianthum are compatible with the synthesis, transport and deposition of suberin. In terms of ontogenesis and function, the intermediate layers of these nectaries are homologous with the stalks of nectar-secreting trichomes. Abstract: Anticlinal cell wall impregnations are common in trichomatic nectaries and their functions as endodermis-like barriers have been discussed because of possible direct effects on the nectary physiology, mainly in the nectar secretion and resorption. However, the cytological events linked to nectary wall impregnations remain little explored. This study documents the ontogenesis and the fine structure of the EFN cells, and cytological events linked to the wall impregnations of multi-layered extrafloral nectaries (EFNs) in Citharexylum myrianthum Cham. (Verbenaceae). EFNs are patelliform, and differentiated into (a) a multicellular foot, which is compound in structure and vascularised with phloem strands, (b) a bi-layered intermediate region with thickened cell walls and (c) a single-layered secretory region with palisade-like cells. EFNs are protodermal in origin, starting with a single protodermal cell and ending with the complex, multi-layered structure. The cell wall impregnations first appear in the very young EFN and increase towards maturity. Lipid patches (assumed to be suberin) are deposited on the inner faces of the primary walls, first along the anticlinal walls and then extend to the periclinal walls. On both walls, plasmodesmata remain apparently intact during the maturation of the EFNs. In the peripheral cytoplasm there are abundant polymorphic plastids, well-developed Golgi bodies often close to rough endoplasmic reticulum profiles, mitochondria and polyribosomes. Cytological events linked to the wall impregnations are consistent with suberin synthesis, transport and deposition. Our findings offer new insights into the structure-properties of specialised nectary cell walls and so should contribute to our knowledge of the physiological and protective roles of this structure in nectar glands.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Centre of Electron Microscopy (CME) Institute of Biosciences of Botucatu (IBB) São Paulo State University (UNESP)Department of Biostatistics Plant Biology Parasitology and Zoology Institute of Biosciences of Botucatu (IBB) São Paulo State University (UNESP)Centre of Electron Microscopy (CME) Institute of Biosciences of Botucatu (IBB) São Paulo State University (UNESP)Department of Biostatistics Plant Biology Parasitology and Zoology Institute of Biosciences of Botucatu (IBB) São Paulo State University (UNESP)CNPq: 303981/2018-0CNPq: 308982/2020-7CNPq: 401053/2016-4Universidade Estadual Paulista (UNESP)Machado, Silvia Rodrigues [UNESP]Rodrigues, Tatiane Maria [UNESP]2022-04-29T08:30:15Z2022-04-29T08:30:15Z2021-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s00425-021-03663-8Planta, v. 254, n. 2, 2021.1432-20480032-0935http://hdl.handle.net/11449/22907510.1007/s00425-021-03663-82-s2.0-85109070793Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlantainfo:eu-repo/semantics/openAccess2024-04-11T19:33:51Zoai:repositorio.unesp.br:11449/229075Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:08:34.223267Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
title Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
spellingShingle Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
Machado, Silvia Rodrigues [UNESP]
Cell wall impregnation
Lipid barrier
Nectar secretion
Patelliform extrafloral nectary
Ultrastructure
title_short Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
title_full Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
title_fullStr Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
title_full_unstemmed Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
title_sort Apoplasmic barrier in the extrafloral nectary of Citharexylum myrianthum (Verbenaceae)
author Machado, Silvia Rodrigues [UNESP]
author_facet Machado, Silvia Rodrigues [UNESP]
Rodrigues, Tatiane Maria [UNESP]
author_role author
author2 Rodrigues, Tatiane Maria [UNESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Machado, Silvia Rodrigues [UNESP]
Rodrigues, Tatiane Maria [UNESP]
dc.subject.por.fl_str_mv Cell wall impregnation
Lipid barrier
Nectar secretion
Patelliform extrafloral nectary
Ultrastructure
topic Cell wall impregnation
Lipid barrier
Nectar secretion
Patelliform extrafloral nectary
Ultrastructure
description Main conclusion: The cytological changes underlying the formation of an apoplasmic barrier in the multi-layered extrafloral nectaries of Citharexylum myrianthum are compatible with the synthesis, transport and deposition of suberin. In terms of ontogenesis and function, the intermediate layers of these nectaries are homologous with the stalks of nectar-secreting trichomes. Abstract: Anticlinal cell wall impregnations are common in trichomatic nectaries and their functions as endodermis-like barriers have been discussed because of possible direct effects on the nectary physiology, mainly in the nectar secretion and resorption. However, the cytological events linked to nectary wall impregnations remain little explored. This study documents the ontogenesis and the fine structure of the EFN cells, and cytological events linked to the wall impregnations of multi-layered extrafloral nectaries (EFNs) in Citharexylum myrianthum Cham. (Verbenaceae). EFNs are patelliform, and differentiated into (a) a multicellular foot, which is compound in structure and vascularised with phloem strands, (b) a bi-layered intermediate region with thickened cell walls and (c) a single-layered secretory region with palisade-like cells. EFNs are protodermal in origin, starting with a single protodermal cell and ending with the complex, multi-layered structure. The cell wall impregnations first appear in the very young EFN and increase towards maturity. Lipid patches (assumed to be suberin) are deposited on the inner faces of the primary walls, first along the anticlinal walls and then extend to the periclinal walls. On both walls, plasmodesmata remain apparently intact during the maturation of the EFNs. In the peripheral cytoplasm there are abundant polymorphic plastids, well-developed Golgi bodies often close to rough endoplasmic reticulum profiles, mitochondria and polyribosomes. Cytological events linked to the wall impregnations are consistent with suberin synthesis, transport and deposition. Our findings offer new insights into the structure-properties of specialised nectary cell walls and so should contribute to our knowledge of the physiological and protective roles of this structure in nectar glands.
publishDate 2021
dc.date.none.fl_str_mv 2021-08-01
2022-04-29T08:30:15Z
2022-04-29T08:30:15Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s00425-021-03663-8
Planta, v. 254, n. 2, 2021.
1432-2048
0032-0935
http://hdl.handle.net/11449/229075
10.1007/s00425-021-03663-8
2-s2.0-85109070793
url http://dx.doi.org/10.1007/s00425-021-03663-8
http://hdl.handle.net/11449/229075
identifier_str_mv Planta, v. 254, n. 2, 2021.
1432-2048
0032-0935
10.1007/s00425-021-03663-8
2-s2.0-85109070793
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Planta
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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