Suppr超能文献

用于小鼠耳蜗三维培养的蛋白质工程水凝胶封装

Protein-engineered hydrogel encapsulation for 3-D culture of murine cochlea.

作者信息

Chang David T, Chai Renjie, DiMarco Rebecca, Heilshorn Sarah C, Cheng Alan G

机构信息

*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.

出版信息

Otol Neurotol. 2015 Mar;36(3):531-8. doi: 10.1097/MAO.0000000000000518.

Abstract

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.

摘要

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。

相似文献

1
Protein-engineered hydrogel encapsulation for 3-D culture of murine cochlea.
Otol Neurotol. 2015 Mar;36(3):531-8. doi: 10.1097/MAO.0000000000000518.
2
BMP signaling is necessary for patterning the sensory and nonsensory regions of the developing mammalian cochlea.
J Neurosci. 2010 Nov 10;30(45):15044-51. doi: 10.1523/JNEUROSCI.3547-10.2010.
3
Peptide- and collagen-based hydrogel substrates for in vitro culture of chick cochleae.
Biomaterials. 2008 Mar;29(8):1028-42. doi: 10.1016/j.biomaterials.2007.11.006. Epub 2007 Nov 26.
4
An in vitro preparation to access cellular and neuronal components in the mouse inner ear.
J Neurocytol. 2000 Sep;29(9):645-52. doi: 10.1023/a:1010831303845.
5
Math1 gene transfer generates new cochlear hair cells in mature guinea pigs in vivo.
J Neurosci. 2003 Jun 1;23(11):4395-400. doi: 10.1523/JNEUROSCI.23-11-04395.2003.
6
Hair cell differentiation in the developing chick cochlea and in embryonic cochlear organ culture.
J Comp Neurol. 1991 Dec 15;314(3):614-25. doi: 10.1002/cne.903140315.
7
β-Catenin is required for radial cell patterning and identity in the developing mouse cochlea.
Proc Natl Acad Sci U S A. 2019 Oct 15;116(42):21054-21060. doi: 10.1073/pnas.1910223116. Epub 2019 Sep 30.
8
Expression of , , and in the mature cochlea reprograms nonsensory cells into hair cells.
Proc Natl Acad Sci U S A. 2024 Jan 30;121(5):e2304680121. doi: 10.1073/pnas.2304680121. Epub 2024 Jan 24.
9
Transfection of mouse cochlear explants by electroporation.
Curr Protoc Neurosci. 2010 Apr;Chapter 4:Unit 4.34.1-10. doi: 10.1002/0471142301.ns0434s51.
10
Primary culture and plasmid electroporation of the murine organ of Corti.
J Vis Exp. 2010 Feb 4(36):1685. doi: 10.3791/1685.

引用本文的文献

1
Optimizing Factors in Murine Whole-Organ Cochlea Culture.
Int J Mol Sci. 2025 Apr 21;26(8):3908. doi: 10.3390/ijms26083908.
2
Enhancing Peptide Biomaterials for Biofabrication.
Polymers (Basel). 2021 Aug 4;13(16):2590. doi: 10.3390/polym13162590.
3
Protein-Engineered Functional Materials.
Adv Healthc Mater. 2019 Jun;8(11):e1801374. doi: 10.1002/adhm.201801374. Epub 2019 Apr 2.
4
Approaches for the study of epigenetic modifications in the inner ear and related tissues.
Hear Res. 2019 May;376:69-85. doi: 10.1016/j.heares.2019.01.007. Epub 2019 Jan 12.
5
In vitro culture of mammalian inner ear hair cells.
J Zhejiang Univ Sci B. 2019;20(2):170-179. doi: 10.1631/jzus.B1700613. Epub 2018 Sep 6.

本文引用的文献

1
3D cell culture systems modeling tumor growth determinants in cancer target discovery.
Adv Drug Deliv Rev. 2014 Apr;69-70:29-41. doi: 10.1016/j.addr.2014.03.001. Epub 2014 Mar 15.
2
Three-dimensional cell culture technique and pathophysiology.
Adv Drug Deliv Rev. 2014 Jul;74:95-103. doi: 10.1016/j.addr.2014.01.003. Epub 2014 Jan 22.
3
The application of 3D cell models to support drug safety assessment: opportunities & challenges.
Adv Drug Deliv Rev. 2014 Apr;69-70:179-89. doi: 10.1016/j.addr.2013.12.005. Epub 2013 Dec 27.
5
Role of cell-matrix interactions on VIC phenotype and tissue deposition in 3D PEG hydrogels.
J Tissue Eng Regen Med. 2016 Oct;10(10):E443-E453. doi: 10.1002/term.1836. Epub 2013 Oct 16.
6
Hydrogels that mimic developmentally relevant matrix and N-cadherin interactions enhance MSC chondrogenesis.
Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10117-22. doi: 10.1073/pnas.1214100110. Epub 2013 Jun 3.
8
A feeder-free, defined three-dimensional polyethylene glycol-based extracellular matrix niche for culture of human embryonic stem cells.
Biomaterials. 2013 May;34(14):3571-80. doi: 10.1016/j.biomaterials.2013.01.073. Epub 2013 Feb 17.
9
A novel role of cytosolic protein synthesis inhibition in aminoglycoside ototoxicity.
J Neurosci. 2013 Feb 13;33(7):3079-93. doi: 10.1523/JNEUROSCI.3430-12.2013.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验