Moazenchi Maedeh, Sadr Hashemi Nejad Anavasadat, Izadi Mahmoud, Khalaj Maedeh, Samsonchi Zakieh, Tavakol Rad Pouya, Amini Payam, Tahamtani Yaser, Hajizadeh-Saffar Ensiyeh
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Advanced Therapy Medicinal Product Technology Development Center (ATMP-TDC), Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Cell J. 2022 Sep 12;24(9):491-499. doi: 10.22074/cellj.2022.8123.
Isolated pancreatic islets are valuable resources for a wide range of research, including cell replacement studies and cell-based platforms for diabetes drug discovery and disease modeling. Islet isolation is a complex and stepwise procedure aiming to obtain pure, viable, and functional islets for in vitro and in vivo studies. It should be noted that differences in rodent strains, gender, weight, and density gradients may affect the isolated islet's properties. We evaluated the variables affecting the rat islet isolation procedure to reach the maximum islet yield and functionality, which would be critical for further studies on islet regenerative biology.
The present experimental study compared the yield and purity of isolated islets from nondiabetic rats of two different strains. Next, islet particle number (IPN) and islet equivalent (IEQ) were compared between males and females, and the weight range that yields the highest number of islets was investigated. Moreover, the influence of three different density gradients, namely Histopaque, Pancoll, and Lymphodex, on final isolated islets purity and yield were assessed. Finally, the viability and functionality of isolated islets were measured.
The IEQ, IPN, and purity of isolated islets in 15 Lister hooded rats (LHRs) were significantly (P≤0.05) higher than those of the other strains. Male LHRs resulted in significantly higher IEQ compared to females (P≤0.05). Moreover, IPN and IEQ did not significantly vary among different weight groups. Also, the utilization of Histopaque and Pancoll leads to higher yield and purity. In vivo assessments of the isolated islets presented significantly reduced blood glucose percentage in the transplanted group on days 2-5 following transplantation.
Based on these results, an optimal protocol for isolating high-quality rat islets with a constant yield, purity, and function has been established as an essential platform for developing diabetes research.
分离的胰岛是广泛研究的宝贵资源,包括细胞替代研究以及用于糖尿病药物发现和疾病建模的基于细胞的平台。胰岛分离是一个复杂的逐步过程,旨在获得用于体外和体内研究的纯净、有活力且功能正常的胰岛。应当注意,啮齿动物品系、性别、体重和密度梯度的差异可能会影响分离出的胰岛的特性。我们评估了影响大鼠胰岛分离过程的变量,以实现最大的胰岛产量和功能,这对于胰岛再生生物学的进一步研究至关重要。
本实验研究比较了两种不同品系非糖尿病大鼠分离出的胰岛的产量和纯度。接下来,比较了雄性和雌性之间的胰岛颗粒数(IPN)和胰岛当量(IEQ),并研究了产生最高胰岛数量的体重范围。此外,评估了三种不同密度梯度,即Histopaque、Pancoll和Lymphodex,对最终分离出的胰岛纯度和产量的影响。最后,测量了分离出的胰岛的活力和功能。
15只利斯特戴帽大鼠(LHRs)分离出的胰岛的IEQ、IPN和纯度显著(P≤0.05)高于其他品系。与雌性相比,雄性LHRs的IEQ显著更高(P≤0.05)。此外,不同体重组之间的IPN和IEQ没有显著差异。而且,使用Histopaque和Pancoll可提高产量和纯度。对分离出的胰岛的体内评估显示,移植组在移植后第2至5天血糖百分比显著降低。
基于这些结果,已建立了一种用于分离具有恒定产量、纯度和功能的高质量大鼠胰岛的优化方案,作为开展糖尿病研究的重要平台。