StemoniX, La Jolla, CA 92037, USA.
Center for Discovery and Innovation in Parasitic Diseases, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA 92093, USA.
Int J Mol Sci. 2021 Feb 14;22(4):1908. doi: 10.3390/ijms22041908.
With increasing global health threats has come an urgent need to rapidly develop and deploy safe and effective therapies. A common practice to fast track clinical adoption of compounds for new indications is to repurpose already approved therapeutics; however, many compounds considered safe to a specific application or population may elicit undesirable side effects when the dosage, usage directives, and/or clinical context are changed. For example, progenitor and developing cells may have different susceptibilities than mature dormant cells, which may yet be different than mature active cells. Thus, in vitro test systems should reflect the cellular context of the native cell: developing, nascent, or functionally active. To that end, we have developed high-throughput, two- and three-dimensional human induced pluripotent stem cell (hiPSC)-derived neural screening platforms that reflect different neurodevelopmental stages. As a proof of concept, we implemented this in vitro human system to swiftly identify the potential neurotoxicity profiles of 29 therapeutic compounds that could be repurposed as anti-virals. Interestingly, many compounds displayed high toxicity on early-stage neural tissues but not on later stages. Compounds with the safest overall viability profiles were further evaluated for functional assessment in a high-throughput calcium flux assay. Of the 29 drugs tested, only four did not modulate or have other potentially toxic effects on the developing or mature neurospheroids across all the tested dosages. These results highlight the importance of employing human neural cultures at different stages of development to fully understand the neurotoxicity profile of potential therapeutics across normal ontogeny.
随着全球健康威胁的增加,迫切需要快速开发和部署安全有效的治疗方法。一种快速将化合物用于新适应症的临床应用的常见做法是重新利用已批准的治疗药物;然而,许多在特定应用或人群中被认为是安全的化合物,当剂量、使用说明和/或临床环境发生变化时,可能会产生不良的副作用。例如,祖细胞和发育中的细胞可能比成熟休眠细胞更敏感,而成熟休眠细胞可能又与成熟活跃细胞不同。因此,体外测试系统应该反映天然细胞的细胞环境:发育中、新生或功能活跃。为此,我们开发了高通量的二维和三维人诱导多能干细胞(hiPSC)衍生的神经筛选平台,反映了不同的神经发育阶段。作为概念验证,我们将这种体外人类系统应用于快速识别 29 种可重新用于抗病毒治疗的潜在神经毒性化合物的特征。有趣的是,许多化合物对早期神经组织显示出高毒性,但对晚期神经组织没有毒性。具有最安全整体存活特征的化合物进一步在高通量钙通量测定中进行了功能评估。在测试的 29 种药物中,只有 4 种药物在所有测试剂量下对发育中的或成熟的神经球体都没有调节作用或其他潜在的毒性作用。这些结果强调了在不同发育阶段使用人类神经培养物来全面了解潜在治疗药物在正常个体发育过程中的神经毒性特征的重要性。