Chang David T, Chai Renjie, DiMarco Rebecca, Heilshorn Sarah C, Cheng Alan G
*Department of Otolaryngology-Head and Neck Surgery, Stanford University School of Medicine; and †Departments of Bioengineering, and ‡Materials Science and Engineering, Stanford University School of Engineering, Stanford, California, U.S.A.
Otol Neurotol. 2015 Mar;36(3):531-8. doi: 10.1097/MAO.0000000000000518.
HYPOTHESIS: Elastin-like protein (ELP) hydrogel helps maintain the three-dimensional (3-D) cochlear structure in culture. BACKGROUND: Whole-organ culture of the cochlea is a useful model system facilitating manipulation and analysis of live sensory cells and surrounding nonsensory cells. The precisely organized 3-D cochlear structure demands a culture method that preserves this delicate architecture; however, current methods have not been optimized to serve such a purpose. METHODS: A protein-engineered ELP hydrogel was used to encapsulate organ of Corti isolated from neonatal mice. Cultured cochleae were immunostained for markers of hair cells and supporting cells. Organ of Corti hair cell and supporting cell density and organ dimensions were compared between the ELP and nonencapsulated systems. These culture systems were then compared with noncultured cochlea. RESULTS: After 3 days in vitro, vital dye uptake and immunostaining for sensory and nonsensory cells show that encapsulated cochlea contain viable cells with an organized architecture. In comparison with nonencapsulated cultured cochlea, ELP-encapsulated cochleae exhibit higher densities of hair cells and supporting cells and taller and narrower organ of Corti dimensions that more closely resemble those of noncultured cochleae. However, we found compromised cell viability when the culture period extended beyond 3 days. CONCLUSION: We conclude that the ELP hydrogel can help preserve the 3-D architecture of neonatal cochlea in short-term culture, which may be applicable to in vitro study of the physiology and pathophysiology of the inner ear.
假设:类弹性蛋白(ELP)水凝胶有助于在培养过程中维持三维(3-D)耳蜗结构。 背景:耳蜗全器官培养是一种有用的模型系统,便于对活的感觉细胞和周围的非感觉细胞进行操作和分析。精确组织的三维耳蜗结构需要一种能保留这种精细结构的培养方法;然而,目前的方法尚未优化以实现这一目的。 方法:使用蛋白质工程化的ELP水凝胶包裹从新生小鼠分离的柯蒂氏器。对培养的耳蜗进行免疫染色,以检测毛细胞和支持细胞的标志物。比较ELP系统和未包裹系统中柯蒂氏器毛细胞和支持细胞的密度以及器官尺寸。然后将这些培养系统与未培养的耳蜗进行比较。 结果:体外培养3天后,对感觉细胞和非感觉细胞进行活性染料摄取和免疫染色显示,包裹的耳蜗含有具有有序结构的活细胞。与未包裹的培养耳蜗相比,ELP包裹的耳蜗显示出更高的毛细胞和支持细胞密度,以及更高且更窄的柯蒂氏器尺寸,更类似于未培养的耳蜗。然而,我们发现当培养期超过3天时,细胞活力会受损。 结论:我们得出结论,ELP水凝胶可有助于在短期培养中保留新生耳蜗的三维结构,这可能适用于内耳生理学和病理生理学的体外研究。
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