The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas
Main Author: | |
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Publication Date: | 2024 |
Other Authors: | , , , , , , , , , |
Format: | Other |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.3390/biomimetics9100598 https://hdl.handle.net/11449/304103 |
Summary: | Type 1 diabetes mellitus (T1DM) is a chronic condition primarily managed with insulin replacement, leading to significant treatment costs. Complications include vasculopathy, cardiovascular diseases, nephropathy, neuropathy, and reticulopathy. Pancreatic islet transplantation is an option but its success does not depend solely on adequate vascularization. The main limitations to clinical islet transplantation are the scarcity of human pancreas, the need for immunosuppression, and the inadequacy of the islet isolation process. Despite extensive research, T1DM remains a major global health issue. In 2015, diabetes affected approximately 415 million people, with projected expenditures of USD 1.7 trillion by 2030. Pancreas transplantation faces challenges due to limited organ availability and complex vascularization. T1DM is caused by the autoimmune destruction of insulin-producing pancreatic cells. Advances in biomaterials, particularly the extracellular matrix (ECM), show promise in tissue reconstruction and transplantation, offering structural and regulatory functions critical for cell migration, differentiation, and adhesion. Tissue engineering aims to create bioartificial pancreases integrating insulin-producing cells and suitable frameworks. This involves decellularization and recellularization techniques to develop biological scaffolds. The challenges include replicating the pancreas’s intricate architecture and maintaining cell viability and functionality. Emerging technologies, such as 3D printing and advanced biomaterials, have shown potential in constructing bioartificial organs. ECM components, including collagens and glycoproteins, play essential roles in cell adhesion, migration, and differentiation. Clinical applications focus on developing functional scaffolds for transplantation, with ongoing research addressing immunological responses and long-term efficacy. Pancreatic bioengineering represents a promising avenue for T1DM treatment, requiring further research to ensure successful implementation. |
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The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreasdecellularizationdiabetes mellitusextracellular matrixinsulin-producing cellstissue engineeringType 1 diabetes mellitus (T1DM) is a chronic condition primarily managed with insulin replacement, leading to significant treatment costs. Complications include vasculopathy, cardiovascular diseases, nephropathy, neuropathy, and reticulopathy. Pancreatic islet transplantation is an option but its success does not depend solely on adequate vascularization. The main limitations to clinical islet transplantation are the scarcity of human pancreas, the need for immunosuppression, and the inadequacy of the islet isolation process. Despite extensive research, T1DM remains a major global health issue. In 2015, diabetes affected approximately 415 million people, with projected expenditures of USD 1.7 trillion by 2030. Pancreas transplantation faces challenges due to limited organ availability and complex vascularization. T1DM is caused by the autoimmune destruction of insulin-producing pancreatic cells. Advances in biomaterials, particularly the extracellular matrix (ECM), show promise in tissue reconstruction and transplantation, offering structural and regulatory functions critical for cell migration, differentiation, and adhesion. Tissue engineering aims to create bioartificial pancreases integrating insulin-producing cells and suitable frameworks. This involves decellularization and recellularization techniques to develop biological scaffolds. The challenges include replicating the pancreas’s intricate architecture and maintaining cell viability and functionality. Emerging technologies, such as 3D printing and advanced biomaterials, have shown potential in constructing bioartificial organs. ECM components, including collagens and glycoproteins, play essential roles in cell adhesion, migration, and differentiation. Clinical applications focus on developing functional scaffolds for transplantation, with ongoing research addressing immunological responses and long-term efficacy. Pancreatic bioengineering represents a promising avenue for T1DM treatment, requiring further research to ensure successful implementation.Graduate Program in Anatomy of Domestic and Wild Animals Faculty of Veterinary Medicine and Animal Science University of São Paulo (FMVZ/USP)Postgraduate Department University of Marília (UNIMAR)Postgraduate Program in Structural and Functional Interactions in Rehabilitation University of Marilia (UNIMAR)UNIMAR Beneficent Hospital (HBU) Medical School University of Marilia (UNIMAR)Department of Animal Morphology and Physiology Faculty of Agricultural and Veterinary Sciences São Paulo State UniversityMedical School University Center of Adamantina (UNIFAI)Department of Biological Sciences Bauru School of Dentistry (FOB/USP) University of Sao PauloPostgraduate Program in Animal Health Production and Environment University of Marilia (UNIMAR)Department of Animal Morphology and Physiology Faculty of Agricultural and Veterinary Sciences São Paulo State UniversityUniversidade de São Paulo (USP)University of Marília (UNIMAR)University of Marilia (UNIMAR)Universidade Estadual Paulista (UNESP)University Center of Adamantina (UNIFAI)Santos da Silva, ThamiresSilva-Júnior, Leandro Norberto daHorvath-Pereira, Bianca de OliveiraValbão, Maria Carolina MiglinoGarcia, Matheus Henrique HerminioLopes, Juliana BarbosaReis, Carlos Henrique BertoniBarreto, Rodrigo da Silva Nunes [UNESP]Buchaim, Daniela VieiraBuchaim, Rogerio LeoneMiglino, Maria Angelica2025-04-29T19:33:53Z2024-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/otherhttp://dx.doi.org/10.3390/biomimetics9100598Biomimetics, v. 9, n. 10, 2024.2313-7673https://hdl.handle.net/11449/30410310.3390/biomimetics91005982-s2.0-85207674493Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiomimeticsinfo:eu-repo/semantics/openAccess2025-04-30T14:24:40Zoai:repositorio.unesp.br:11449/304103Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T14:24:40Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
title |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
spellingShingle |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas Santos da Silva, Thamires decellularization diabetes mellitus extracellular matrix insulin-producing cells tissue engineering |
title_short |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
title_full |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
title_fullStr |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
title_full_unstemmed |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
title_sort |
The Role of the Pancreatic Extracellular Matrix as a Tissue Engineering Support for the Bioartificial Pancreas |
author |
Santos da Silva, Thamires |
author_facet |
Santos da Silva, Thamires Silva-Júnior, Leandro Norberto da Horvath-Pereira, Bianca de Oliveira Valbão, Maria Carolina Miglino Garcia, Matheus Henrique Herminio Lopes, Juliana Barbosa Reis, Carlos Henrique Bertoni Barreto, Rodrigo da Silva Nunes [UNESP] Buchaim, Daniela Vieira Buchaim, Rogerio Leone Miglino, Maria Angelica |
author_role |
author |
author2 |
Silva-Júnior, Leandro Norberto da Horvath-Pereira, Bianca de Oliveira Valbão, Maria Carolina Miglino Garcia, Matheus Henrique Herminio Lopes, Juliana Barbosa Reis, Carlos Henrique Bertoni Barreto, Rodrigo da Silva Nunes [UNESP] Buchaim, Daniela Vieira Buchaim, Rogerio Leone Miglino, Maria Angelica |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) University of Marília (UNIMAR) University of Marilia (UNIMAR) Universidade Estadual Paulista (UNESP) University Center of Adamantina (UNIFAI) |
dc.contributor.author.fl_str_mv |
Santos da Silva, Thamires Silva-Júnior, Leandro Norberto da Horvath-Pereira, Bianca de Oliveira Valbão, Maria Carolina Miglino Garcia, Matheus Henrique Herminio Lopes, Juliana Barbosa Reis, Carlos Henrique Bertoni Barreto, Rodrigo da Silva Nunes [UNESP] Buchaim, Daniela Vieira Buchaim, Rogerio Leone Miglino, Maria Angelica |
dc.subject.por.fl_str_mv |
decellularization diabetes mellitus extracellular matrix insulin-producing cells tissue engineering |
topic |
decellularization diabetes mellitus extracellular matrix insulin-producing cells tissue engineering |
description |
Type 1 diabetes mellitus (T1DM) is a chronic condition primarily managed with insulin replacement, leading to significant treatment costs. Complications include vasculopathy, cardiovascular diseases, nephropathy, neuropathy, and reticulopathy. Pancreatic islet transplantation is an option but its success does not depend solely on adequate vascularization. The main limitations to clinical islet transplantation are the scarcity of human pancreas, the need for immunosuppression, and the inadequacy of the islet isolation process. Despite extensive research, T1DM remains a major global health issue. In 2015, diabetes affected approximately 415 million people, with projected expenditures of USD 1.7 trillion by 2030. Pancreas transplantation faces challenges due to limited organ availability and complex vascularization. T1DM is caused by the autoimmune destruction of insulin-producing pancreatic cells. Advances in biomaterials, particularly the extracellular matrix (ECM), show promise in tissue reconstruction and transplantation, offering structural and regulatory functions critical for cell migration, differentiation, and adhesion. Tissue engineering aims to create bioartificial pancreases integrating insulin-producing cells and suitable frameworks. This involves decellularization and recellularization techniques to develop biological scaffolds. The challenges include replicating the pancreas’s intricate architecture and maintaining cell viability and functionality. Emerging technologies, such as 3D printing and advanced biomaterials, have shown potential in constructing bioartificial organs. ECM components, including collagens and glycoproteins, play essential roles in cell adhesion, migration, and differentiation. Clinical applications focus on developing functional scaffolds for transplantation, with ongoing research addressing immunological responses and long-term efficacy. Pancreatic bioengineering represents a promising avenue for T1DM treatment, requiring further research to ensure successful implementation. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-10-01 2025-04-29T19:33:53Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/other |
format |
other |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3390/biomimetics9100598 Biomimetics, v. 9, n. 10, 2024. 2313-7673 https://hdl.handle.net/11449/304103 10.3390/biomimetics9100598 2-s2.0-85207674493 |
url |
http://dx.doi.org/10.3390/biomimetics9100598 https://hdl.handle.net/11449/304103 |
identifier_str_mv |
Biomimetics, v. 9, n. 10, 2024. 2313-7673 10.3390/biomimetics9100598 2-s2.0-85207674493 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Biomimetics |
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 |
repositoriounesp@unesp.br |
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1834482507897110528 |