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Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold

We reported in 2018 that among several extracellular matrices, fibronectin, type I collagen, type IV collagen, laminin I, fibrinogen, and bovine serum albumin, fibronectin is particularly useful for adhesion of porcine pancreatic tissue. Subsequently, we developed a technology that enables the chemi...

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Autores principales: Nakashima, Yoshiki, Iguchi, Hiroki, Takakura, Kenta, Nakamura, Yuta, Izumi, Kenji, Koba, Naoya, Haneda, Satoshi, Tsukahara, Masayoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449504/
https://www.ncbi.nlm.nih.gov/pubmed/36062469
http://dx.doi.org/10.1177/09636897221120500
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author Nakashima, Yoshiki
Iguchi, Hiroki
Takakura, Kenta
Nakamura, Yuta
Izumi, Kenji
Koba, Naoya
Haneda, Satoshi
Tsukahara, Masayoshi
author_facet Nakashima, Yoshiki
Iguchi, Hiroki
Takakura, Kenta
Nakamura, Yuta
Izumi, Kenji
Koba, Naoya
Haneda, Satoshi
Tsukahara, Masayoshi
author_sort Nakashima, Yoshiki
collection PubMed
description We reported in 2018 that among several extracellular matrices, fibronectin, type I collagen, type IV collagen, laminin I, fibrinogen, and bovine serum albumin, fibronectin is particularly useful for adhesion of porcine pancreatic tissue. Subsequently, we developed a technology that enables the chemical coating of the constituent motifs of fibronectin onto cell culture dishes. In this experiment, we used islets (purity ≥ 90%), duct epithelial cells (purity ≥ 60%), and acinar cells (purity ≥ 99%) isolated from human pancreas according to the Edmonton protocol published in 2000 and achieved adhesion to the constituent motifs of fibronectin. A solution including cGMP Prodo Islet Media was used as the assay solution. In islets, adhesion was enhanced with the constitutive motifs of fibronectin compared with uncoated islets. In the functional evaluation of islets, insulin mRNA expression and insulin secretion were enhanced by the constitutive motif of fibronectin compared with non-coated islets. The stimulation index was comparable between non-coated islets and fibronectin motifs. In duct epithelial cells, adhesion was mildly promoted by the fibronectin component compared with non-coated component, while in acinar cells, adhesion was inhibited by the fibronectin component compared with the non-coated component. These data suggest that the constitutive motifs of fibronectin are useful for the adhesion of islets and duct epithelial cells.
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spelling pubmed-94495042022-09-08 Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold Nakashima, Yoshiki Iguchi, Hiroki Takakura, Kenta Nakamura, Yuta Izumi, Kenji Koba, Naoya Haneda, Satoshi Tsukahara, Masayoshi Cell Transplant Original Article We reported in 2018 that among several extracellular matrices, fibronectin, type I collagen, type IV collagen, laminin I, fibrinogen, and bovine serum albumin, fibronectin is particularly useful for adhesion of porcine pancreatic tissue. Subsequently, we developed a technology that enables the chemical coating of the constituent motifs of fibronectin onto cell culture dishes. In this experiment, we used islets (purity ≥ 90%), duct epithelial cells (purity ≥ 60%), and acinar cells (purity ≥ 99%) isolated from human pancreas according to the Edmonton protocol published in 2000 and achieved adhesion to the constituent motifs of fibronectin. A solution including cGMP Prodo Islet Media was used as the assay solution. In islets, adhesion was enhanced with the constitutive motifs of fibronectin compared with uncoated islets. In the functional evaluation of islets, insulin mRNA expression and insulin secretion were enhanced by the constitutive motif of fibronectin compared with non-coated islets. The stimulation index was comparable between non-coated islets and fibronectin motifs. In duct epithelial cells, adhesion was mildly promoted by the fibronectin component compared with non-coated component, while in acinar cells, adhesion was inhibited by the fibronectin component compared with the non-coated component. These data suggest that the constitutive motifs of fibronectin are useful for the adhesion of islets and duct epithelial cells. SAGE Publications 2022-09-05 /pmc/articles/PMC9449504/ /pubmed/36062469 http://dx.doi.org/10.1177/09636897221120500 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Nakashima, Yoshiki
Iguchi, Hiroki
Takakura, Kenta
Nakamura, Yuta
Izumi, Kenji
Koba, Naoya
Haneda, Satoshi
Tsukahara, Masayoshi
Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold
title Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold
title_full Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold
title_fullStr Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold
title_full_unstemmed Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold
title_short Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold
title_sort adhesion characteristics of human pancreatic islets, duct epithelial cells, and acinar cells to a polymer scaffold
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449504/
https://www.ncbi.nlm.nih.gov/pubmed/36062469
http://dx.doi.org/10.1177/09636897221120500
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