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内脏间皮糖萼的结构杂多糖黏附。

Structural Heteropolysaccharide Adhesion to the Glycocalyx of Visceral Mesothelium.

机构信息

1 Laboratory of Adaptive and Regenerative Biology, Brigham and Women's Hospital , Harvard Medical School, Boston, Massachusetts.

2 Institute of Functional and Clinical Anatomy, University Medical Center of the Johannes Gutenberg-University , Mainz, Germany .

出版信息

Tissue Eng Part A. 2018 Feb;24(3-4):199-206. doi: 10.1089/ten.TEA.2017.0042. Epub 2017 Jun 30.

Abstract

Bioadhesives are biopolymers with potential applications in wound healing, drug delivery, and tissue engineering. Pectin, a plant-based heteropolysaccharide, has recently demonstrated potential as a mucoadhesive in the gut. Since mucoadhesion is a process likely involving the interpenetration of the pectin polymer with mucin chains, we hypothesized that pectin may also be effective at targeting the glycocalyx of the visceral mesothelium. To explore the potential role of pectin as a mesothelial bioadhesive, we studied the interaction of various pectin formulations with the mesothelium of the lung, liver, bowel, and heart. Tensile strength, peel strength, and shear resistance of the bioadhesive-mesothelial interaction were measured by load/displacement measurements. In both high-methoxyl pectins (HMP) and low-methoxyl pectins, bioadhesion was greatest with an equal weight % formulation with carboxymethylcellulose (CMC). The tensile strength of the high-methoxyl pectin was consistently greater than low-methoxyl or amidated low-methoxyl formulations (p < 0.05). Consistent with a mechanism of polymer-glycocalyx interpenetration, the HMP adhesion to tissue mesothelium was reversed with hydration and limited by enzyme treatment (hyaluronidase, pronase, and neuraminidase). Peel and shear forces applied to the lung/pectin adhesion resulted in a near-interface structural failure and the efficient isolation of intact en face pleural mesothelium. These data indicate that HMP, in an equal weight % mixture with CMC, is a promising mesothelial bioadhesive for use in experimental and therapeutic applications.

摘要

生物黏附剂是具有潜在应用价值的生物聚合物,可用于伤口愈合、药物输送和组织工程。果胶是一种植物源杂多糖,最近在肠道黏附方面显示出潜力。由于黏附是一个聚合物与黏蛋白链相互渗透的过程,我们假设果胶也可能有效地靶向内脏间皮的糖萼。为了探索果胶作为间皮生物黏附剂的潜在作用,我们研究了各种果胶配方与肺、肝、肠和心脏间皮的相互作用。通过负载/位移测量来测量生物黏附-间皮相互作用的拉伸强度、剥离强度和抗剪强度。在高甲氧基果胶 (HMP) 和低甲氧基果胶中,与羧甲基纤维素 (CMC) 等重量%配方的生物黏附性最强。高甲氧基果胶的拉伸强度始终大于低甲氧基果胶或酰胺化低甲氧基果胶配方(p < 0.05)。与聚合物-糖萼相互渗透的机制一致,HMP 对组织间皮的黏附作用被水合作用逆转,并受到酶处理(透明质酸酶、蛋白酶和神经氨酸酶)的限制。施加在肺/果胶黏附物上的剥离和剪切力导致近界面结构失效,并有效地分离完整的胸膜间皮。这些数据表明,HMP 与 CMC 以等重量%的混合物形式,是一种有前途的间皮生物黏附剂,可用于实验和治疗应用。

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