Salamone Monica, Rigogliuso Salvatrice, Nicosia Aldo, Campora Simona, Bruno Carmelo Marco, Ghersi Giulio
Abiel s.r.l., c/o Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF) University of Palermo, Viale delle Scienze, Ed. 16, 90128 Palermo, Italy.
Institute for Biomedical Research and Innovation-National Research Council (IRIB-CNR), Via Ugo La Malfa 153, 90146 Palermo, Italy.
Biomedicines. 2021 Jun 27;9(7):739. doi: 10.3390/biomedicines9070739.
Adipose derived microvascular fragments (ad-MVFs) consist of effective vascularization units able to reassemble into efficient microvascular networks. Because of their content in stem cells and related angiogenic activity, ad-MVFs represent an interesting tool for applications in regenerative medicine. Here we show that gentle dissociation of rat adipose tissue provides a mixture of ad-MVFs with a length distribution ranging from 33-955 μm that are able to maintain their original morphology. The isolated units of ad-MVFs that resulted were able to activate transcriptional switching toward angiogenesis, forming tubes, branches, and entire capillary networks when cultured in 3D collagen type-I hydrogel. The proper involvement of metalloproteases (MMP2/MMP9) and serine proteases in basal lamina and extracellular matrix ECM degradation during the angiogenesis were concurrently assessed by the evaluation of alpha-smooth muscle actin (αSMA) expression. These results suggest that collagen type-I hydrogel provides an adequate 3D environment supporting the activation of the vascularization process. As a proof of concept, we exploited 3D collagen hydrogel for the setting of ad-MVF-islet of Langerhans coculture to improve the islets vascularization. Our results suggest potential employment of the proposed in vitro system for regenerative medicine applications, such as the improving of the islet of Langerhans engraftment before transplantation.
脂肪来源的微血管片段(ad-MVFs)由能够重新组装成高效微血管网络的有效血管化单元组成。由于其干细胞含量和相关血管生成活性,ad-MVFs是再生医学应用中一种有趣的工具。在这里,我们表明,大鼠脂肪组织的温和解离提供了一种长度分布在33 - 955μm之间的ad-MVFs混合物,这些混合物能够保持其原始形态。所得到的分离的ad-MVFs单元能够激活向血管生成的转录转换,当在三维I型胶原水凝胶中培养时,形成管、分支和完整的毛细血管网络。通过评估α-平滑肌肌动蛋白(αSMA)的表达,同时评估了金属蛋白酶(MMP2/MMP9)和丝氨酸蛋白酶在血管生成过程中对基膜和细胞外基质ECM降解的适当参与。这些结果表明,I型胶原水凝胶提供了一个支持血管化过程激活的合适三维环境。作为概念验证,我们利用三维胶原水凝胶来设置ad-MVF-胰岛共培养,以改善胰岛的血管化。我们的结果表明,所提出的体外系统在再生医学应用中具有潜在的用途,例如在移植前改善胰岛的植入。