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人小梁网器官培养。一种新方法。

Human trabecular meshwork organ culture. A new method.

作者信息

Johnson D H, Tschumper R C

出版信息

Invest Ophthalmol Vis Sci. 1987 Jun;28(6):945-53.

PMID:3583633
Abstract

A new method has been developed for organ culture of human trabecular meshwork. Human eyebank eyes are sectioned at the equator and lens and vitreous are removed. The anterior segments are placed in a modified culture dish, cornea side up, and then sealed in place. Culture media (Dulbecco's modified Eagle media) are perfused through a cannula built into the bottom of the dish. The sealed system forces media to flow through the trabecular meshwork, Schlemm's canal, and exit through the normal limbal pathways. Intraocular pressure can be maintained at normal (or elevated) levels throughout the culture period. Corneal clarity is maintained. Trabecular cells remain in normal position on trabecular beams and maintain many of their usual morphologic characteristics. Cultures appear to be viable for up to 4 weeks. This technique should allow study of intact human trabecular meshwork in a controlled experimental fashion.

摘要

一种用于人小梁网器官培养的新方法已经被开发出来。从人类眼库获取的眼球在赤道处切开,移除晶状体和玻璃体。将前段部分角膜面朝上放置在一个改良的培养皿中,然后固定密封。通过内置在培养皿底部的插管灌注培养基(杜尔贝科改良伊格尔培养基)。密封系统迫使培养基流经小梁网、施莱姆管,并通过正常的角膜缘途径流出。在整个培养期间,眼内压可以维持在正常(或升高)水平。角膜保持透明。小梁细胞在小梁束上保持正常位置,并维持许多其通常的形态学特征。培养物在长达4周的时间内似乎都具有活性。这项技术应该能够以可控的实验方式对完整的人小梁网进行研究。

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