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交联血红蛋白对微囊化胰岛功能和活力的影响。

Effect of cross-linked hemoglobin on functionality and viability of microencapsulated pancreatic islets.

作者信息

Chae Su Young, Kim Sung Wan, Bae You Han

机构信息

Center for Biomaterials and Biotechnology, Department of Materials Science and Engineering, Kwangju Institute of Science and Technology, Kwangju, South Korea.

出版信息

Tissue Eng. 2002 Jul;8(3):379-94. doi: 10.1089/107632702760184655.

Abstract

Of many obstacles involved in developing a bioartificial pancreas, which consists of encapsulated and physically immunoprotected islets, for long-term implantation in insulin-dependent diabetic patients, the impaired functionality and decreasing viability of encapsulated islets over time are critical factors in determining the size and longevity of the implant. These factors are closely associated with short oxygen supply to the encaged islets from the implant site. To facilitate oxygen transport to islets in the capsules, we coencapsulated hemoglobin cross-linked with difunctional polyethylene glycol (Hb-conjugate, Hb-C) which is large in size (>100 kDa), thus preventing diffusional loss through the immunoprotecting membrane. The coencapsulation of Hb-C with islets in alginate-poly-L-lysine microcapsules by dissolving Hb-C in an islet-suspended alginate solution at a concentration of 0.25 mM improved the insulin secretion and viability of the islets. At week 0, the islets, coencapsulated with Hb-C, cultured at P(O2) = 40 mmHg (assumed oxygen partial pressure in the most common implant site, the peritoneal cavity), secreted 200% more insulin compared with the control islets without Hb-C at glucose concentrations of both 100 and 300 mg/dL. The Hb-C effect became more significant with time at higher glucose concentrations. After culturing the islets for 8 weeks at 40 mmHg, the insulin secretion was enhanced 200 and 550% at glucose concentrations of 100 and 300 mg/dL as compared with the control, respectively. The results were closely associated with improved viability and suggest that the introduction of Hb-C is an effective approach to maintaining the oxygen supply to encapsulated islets. In addition, Hb-C coencapsulation with pancreatic islets may (1) provide a partial clue to reducing the large size of the biohybrid artificial pancreas, (2) lead to a reduced need for pancreas donation, and (3) prolong the longevity of the biohybrid artificial pancreas in the body.

摘要

在开发一种生物人工胰腺的过程中存在诸多障碍,这种生物人工胰腺由包裹起来并在物理上实现免疫保护的胰岛组成,用于长期植入胰岛素依赖型糖尿病患者体内。随着时间推移,包裹的胰岛功能受损和活力下降是决定植入物大小和寿命的关键因素。这些因素与植入部位向被包裹胰岛的氧气供应不足密切相关。为促进氧气向胶囊内胰岛的输送,我们将血红蛋白与双功能聚乙二醇交联(血红蛋白缀合物,Hb-C)共同包裹,该缀合物尺寸较大(>100 kDa),从而防止其通过免疫保护膜扩散流失。通过将Hb-C以0.25 mM的浓度溶解在悬浮有胰岛的海藻酸盐溶液中,在海藻酸盐-聚-L-赖氨酸微胶囊中与胰岛共同包裹Hb-C,改善了胰岛的胰岛素分泌和活力。在第0周时,与不含Hb-C的对照胰岛相比,在P(O2)=40 mmHg(假定为最常见植入部位腹腔的氧分压)条件下培养的、与Hb-C共同包裹的胰岛,在葡萄糖浓度为100和300 mg/dL时分泌的胰岛素多200%。在较高葡萄糖浓度下,随着时间推移Hb-C的作用变得更加显著。在40 mmHg条件下将胰岛培养8周后,与对照组相比,在葡萄糖浓度为100和300 mg/dL时,胰岛素分泌分别增强了200%和550%。这些结果与活力的改善密切相关,表明引入Hb-C是维持向包裹胰岛供氧的有效方法。此外,Hb-C与胰岛共同包裹可能(1)为减小生物杂交人工胰腺的大尺寸提供部分线索,(2)减少对胰腺捐赠的需求,(3)延长生物杂交人工胰腺在体内的寿命。

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