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软骨寡聚基质蛋白-血管生成素-1增强分离胰岛的血管生成并在移植后维持正常血糖水平。

Cartilage oligomeric matrix protein-angiopoientin-1 enhances angiogenesis of isolated islet and maintains normoglycemia following transplantation.

作者信息

Park K S, Shim E Y, Choi B K, Moon C, Kim S H, Kim Y S, Kwon C H, Joh J W, Koh G Y, Kim S J

机构信息

Department of Molecular Medicine, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

出版信息

Transplant Proc. 2010 Sep;42(7):2653-7. doi: 10.1016/j.transproceed.2010.04.048.

Abstract

Islet transplantation (ITx) has potential as a therapy for patients with type 1 diabetes. For successful engraftment and insulin independence, the transplanted islets must establish an adequate, stable blood supply. Angiopoientin-1 (Ang1) is a specific growth factor that induces vascularization via the Tie2 or Tie1 receptor. In this study, we used an in vitro angiogenesis assay to evaluate islet function following transplantation and the effect of the Ang1 variant cartilage oligomeric matrix protein (COMP) Ang1 on isolated islets. The enhanced function of islets transduced with COMP-Ang1 was also confirmed in a streptozotocin (STZ)-induced diabetic mice model. In a three-dimensional collagen-based culture system, the transduction of COMP-Ang1 into islets significantly increased angiogenesis compared with the bacterial-β-galactosidase (LacZ)-transduced controls and an intact, nontransduced islet negative control group. COMP-Ang1 transduced islets also attenuated hyperglycemia in syngeneic diabetic C57BL/6 mice and enhanced glucose tolerance by areas under the curves of intraperitoneal glucose tolerance tests. These findings demonstrated the capacity of COMP-Ang1 to promote revascularization in cultured islets, which may contribute to successful transplantation in vivo.

摘要

胰岛移植(ITx)对1型糖尿病患者具有潜在的治疗作用。为了实现成功植入并实现胰岛素非依赖,移植的胰岛必须建立充足、稳定的血液供应。血管生成素-1(Ang1)是一种通过Tie2或Tie1受体诱导血管形成的特异性生长因子。在本研究中,我们使用体外血管生成试验来评估移植后胰岛的功能以及Ang1变体软骨寡聚基质蛋白(COMP)-Ang1对分离胰岛的影响。在链脲佐菌素(STZ)诱导的糖尿病小鼠模型中也证实了用COMP-Ang1转导的胰岛功能增强。在基于三维胶原蛋白的培养系统中,与细菌β-半乳糖苷酶(LacZ)转导的对照组和完整、未转导的胰岛阴性对照组相比,将COMP-Ang1转导到胰岛中可显著增加血管生成。转导了COMP-Ang1的胰岛还可减轻同基因糖尿病C57BL/6小鼠的高血糖症,并通过腹腔内葡萄糖耐量试验曲线下面积提高葡萄糖耐量。这些发现证明了COMP-Ang1促进培养胰岛血管再生的能力,这可能有助于体内的成功移植。

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