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用于组织工程的表面改性纤维素支架

Surface modified cellulose scaffolds for tissue engineering.

作者信息

Courtenay James C, Johns Marcus A, Galembeck Fernando, Deneke Christoph, Lanzoni Evandro M, Costa Carlos A, Scott Janet L, Sharma Ram I

机构信息

1Centre for Sustainable Chemical Technologies, University of Bath, Claverton Down, Bath, BA2 7AY UK.

2Department of Chemical Engineering, University of Bath, Claverton Down, Bath, BA2 7AY UK.

出版信息

Cellulose (Lond). 2017;24(1):253-267. doi: 10.1007/s10570-016-1111-y. Epub 2016 Nov 9.

DOI:10.1007/s10570-016-1111-y
PMID:32355428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7175690/
Abstract

We report the ability of cellulose to support cells without the use of matrix ligands on the surface of the material, thus creating a two-component system for tissue engineering of cells and materials. Sheets of bacterial cellulose, grown from a culture medium containing organism were chemically modified with glycidyltrimethylammonium chloride or by oxidation with sodium hypochlorite in the presence of sodium bromide and 2,2,6,6-tetramethylpipiridine 1-oxyl radical to introduce a positive, or negative, charge, respectively. This modification process did not degrade the mechanical properties of the bulk material, but grafting of a positively charged moiety to the cellulose surface (cationic cellulose) increased cell attachment by 70% compared to unmodified cellulose, while negatively charged, oxidised cellulose films (anionic cellulose), showed low levels of cell attachment comparable to those seen for unmodified cellulose. Only a minimal level of cationic surface derivitisation (ca 3% degree of substitution) was required for increased cell attachment and mediating proteins were required. Cell adhesion studies exhibited the same trends as the attachment studies, while the mean cell area and aspect ratio was highest on the cationic surfaces. Overall, we demonstrated the utility of positively charged bacterial cellulose in tissue engineering in the absence of proteins for cell attachment.

摘要

我们报道了纤维素在材料表面不使用基质配体的情况下支持细胞的能力,从而创建了一种用于细胞和材料组织工程的双组分系统。从含有生物体的培养基中生长的细菌纤维素片材,用缩水甘油基三甲基氯化铵进行化学修饰,或在溴化钠和2,2,6,6-四甲基哌啶1-氧基自由基存在下用次氯酸钠氧化,分别引入正电荷或负电荷。这种修饰过程没有降低块状材料的机械性能,但与未修饰的纤维素相比,将带正电荷的部分接枝到纤维素表面(阳离子纤维素)使细胞附着增加了70%,而带负电荷的氧化纤维素膜(阴离子纤维素)显示出与未修饰纤维素相当的低水平细胞附着。仅需要最低水平的阳离子表面衍生化(约3%的取代度)即可增加细胞附着,且不需要介导蛋白。细胞黏附研究显示出与附着研究相同的趋势,而阳离子表面上的平均细胞面积和纵横比最高。总体而言,我们证明了在不存在用于细胞附着的蛋白质的情况下,带正电荷的细菌纤维素在组织工程中的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/e3982e35c682/10570_2016_1111_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/171ebd79c300/10570_2016_1111_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/02a81c65a439/10570_2016_1111_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/5d59bbd0f77f/10570_2016_1111_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/eab1ab27221e/10570_2016_1111_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/9e3ca1597357/10570_2016_1111_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/58d33bff9159/10570_2016_1111_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/cd1e0778be5a/10570_2016_1111_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/097e98422a69/10570_2016_1111_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/7f6e347e7081/10570_2016_1111_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/455d1194da6a/10570_2016_1111_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/e3982e35c682/10570_2016_1111_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/171ebd79c300/10570_2016_1111_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/02a81c65a439/10570_2016_1111_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/5d59bbd0f77f/10570_2016_1111_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/eab1ab27221e/10570_2016_1111_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/9e3ca1597357/10570_2016_1111_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/58d33bff9159/10570_2016_1111_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/cd1e0778be5a/10570_2016_1111_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/097e98422a69/10570_2016_1111_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/7f6e347e7081/10570_2016_1111_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/455d1194da6a/10570_2016_1111_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc62/7175690/e3982e35c682/10570_2016_1111_Fig10_HTML.jpg

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