Department of Bioengineering and QB3 Institute, University of California, Berkeley, Berkeley, CA, USA.
Keck Graduate Institute, The Claremont Colleges, Claremont, CA, USA.
Nat Protoc. 2022 Nov;17(11):2469-2493. doi: 10.1038/s41596-022-00731-5. Epub 2022 Aug 19.
We describe a small-animal blood exchange approach developed for aging research as an alternative to heterochronic parabiosis or plasma injections. In parabiosis, animals are surgically coupled, which has several disadvantages, including difficulty controlling experimental procedure, the effects of shared organs, environmental enrichment from jointly exploring the housing enclosure, involuntary exercise and an imprecise onset of blood sharing. Likewise, in plasma injections, the added volumes need to be small, and there is little flexibility in changing the relative contributions of ectopic to endogenous blood components. These factors complicate the conclusions and interpretations, including the identification of key mechanisms and molecular or cellular determinants. Our approach, where blood is exchanged between animals without them being surgically coupled, is less invasive than parabiosis. The percentage of exchanged blood or other exchanged fluids is known and precise. The age of plasma and cells can be mixed and matched at all desired relative contributions to the endogenous systemic milieu, and the onset of the effects can be accurately delineated. In this protocol, we describe the preparatory and animal surgery steps required for small-animal blood exchange in mice and compare this process with parabiosis and plasma injections. We also provide the design, hardware and software for the blood exchange device and compare automated and manual exchange methods. Lastly, we report mathematical modeling of the dilution of blood factors. The fluid exchange takes ~30 min when performed by a well-trained biomedical scientist; the entire process takes ~2 h.
我们描述了一种用于衰老研究的小动物血液交换方法,作为异体共生或血浆注射的替代方法。在异体共生中,动物通过手术连接,这有几个缺点,包括难以控制实验程序、共享器官的影响、从共同探索住房环境中获得的环境丰富、无意识的运动以及血液共享的不准确开始。同样,在血浆注射中,添加的体积需要很小,并且改变异位到内源性血液成分的相对贡献的灵活性很小。这些因素使结论和解释复杂化,包括确定关键机制和分子或细胞决定因素。我们的方法是在不进行手术连接的情况下在动物之间交换血液,这种方法比异体共生侵入性更小。交换的血液或其他交换液的百分比是已知且精确的。可以根据需要以所有期望的相对贡献混合和匹配血浆和细胞的年龄,并且可以准确描绘出效果的开始。在本方案中,我们描述了在小鼠中小动物血液交换所需的准备和动物手术步骤,并将此过程与异体共生和血浆注射进行了比较。我们还提供了血液交换设备的设计、硬件和软件,并比较了自动和手动交换方法。最后,我们报告了血液因子稀释的数学模型。当由训练有素的生物医学科学家执行时,流体交换大约需要 30 分钟;整个过程大约需要 2 小时。