Ryan Anne R, Cleaver Ondine
Department of Molecular Biology, Center for Regenerative Science and Medicine (CRSM), University of Texas Southwestern Medical Center, Dallas, TX, United States.
Department of Molecular Biology, Center for Regenerative Science and Medicine (CRSM), University of Texas Southwestern Medical Center, Dallas, TX, United States.
Curr Top Dev Biol. 2022;148:165-194. doi: 10.1016/bs.ctdb.2022.02.013. Epub 2022 Apr 5.
The formation, growth and maintenance of our organs, such as our kidneys or pancreas, requires their coordinated growth alongside the intricate vasculature that pervades them. Blood vessels course through nearly every tissue in our bodies, facilitating the essential exchange of gases, nutrition and wastes, as well as the rapid circulation of hormones and other signaling molecules. Endothelial cells (ECs) that line all of our blood vessels are therefore the gatekeepers for communication between the circulation and organ-specific cell types. We and many others have sought to understand: (1) how endothelial cell progenitors initially assemble to form blood vessels in the embryo, and (2) how the embryonic vascular tree expands to perfuse growing organs. Here, we review what we have learned from embryonic blood vessels and how this knowledge instructs our approaches to vascularize laboratory generated tissues, such as organoids. We will assess our general understanding of blood vessel formation, and discuss recent studies of the growing kidney vasculature. Furthermore, we will assess the challenges and limitations faced by organoid technologies, including the difficulties in achieving the patterned vascular network that is essential to organ function. Lastly, we will then review recent studies of kidney organoid blood vessels and propose approaches that improve vascularization. Understanding the ontogeny of organ-specific vasculatures will help propel regenerative therapeutic approaches.
我们的器官,如肾脏或胰腺的形成、生长和维持,需要它们与遍布其中的复杂脉管系统协调生长。血管遍布我们身体的几乎每一个组织,促进气体、营养物质和废物的重要交换,以及激素和其他信号分子的快速循环。因此,衬于我们所有血管内的内皮细胞是循环系统与器官特异性细胞类型之间通讯的守门人。我和其他许多人一直在试图弄清楚:(1)内皮细胞祖细胞最初是如何在胚胎中组装形成血管的,以及(2)胚胎血管树是如何扩展以灌注生长中的器官的。在这里,我们回顾我们从胚胎血管中学到的知识,以及这些知识如何指导我们使实验室生成的组织(如类器官)血管化的方法。我们将评估我们对血管形成的总体理解,并讨论关于生长中的肾脏脉管系统的最新研究。此外,我们将评估类器官技术面临的挑战和局限性,包括难以实现对器官功能至关重要的有模式的血管网络。最后,我们将回顾关于肾脏类器官血管的最新研究,并提出改善血管化的方法。了解器官特异性脉管系统的个体发生将有助于推动再生治疗方法的发展。