Yoshida Naoko, Perry Anthony C F
Laboratory of Mammalian Molecular Embryology, RIKEN Center for Developmental Biology, 2-2-3 Minatojima Minamimachi, Chuo-ku, Kobe 650-0047, Japan.
Nat Protoc. 2007;2(2):296-304. doi: 10.1038/nprot.2007.7.
The mouse is a genetically tractable model organism widely used to study mammalian development and disease. However, mouse metaphase II (mII) oocytes are exquisitely sensitive and intracytoplasmic sperm injection (ICSI) with conventional pipettes generally kills them. This problem can be solved with piezo-actuated micromanipulation, in which the piezo-electric effect (crystal deformation in response to an externally applied voltage) propels a microinjection needle tip forward in a precise and rapid movement. Piezo-actuated micromanipulation enhances the penetration of membranes and matrices, and mouse ICSI is a major application. Here we describe a comprehensive, step-by-step mouse piezo ICSI protocol for non-specialists that can be completed in 2-4 h. The protocol is a basic prelude to multiple applications, including nuclear transfer cloning, spermatid injection, blastocyst injection, mII transgenesis, and streamlining micromanipulation in primates and livestock. Moreover, piezo ICSI can be used to obtain offspring from 'dead' (non-motile) sperm, enabling trivial sperm freezing protocols for mouse strain storage and shipment.
小鼠是一种遗传上易于操作的模式生物,被广泛用于研究哺乳动物的发育和疾病。然而,小鼠减数分裂中期II(mII)卵母细胞极其敏感,使用传统移液管进行胞浆内精子注射(ICSI)通常会导致其死亡。这个问题可以通过压电驱动的显微操作来解决,其中压电效应(晶体响应外部施加的电压而变形)使显微注射针尖以精确且快速的运动向前推进。压电驱动的显微操作增强了对膜和基质的穿透能力,小鼠ICSI是其主要应用之一。在此,我们为非专业人员描述了一个全面的、分步的小鼠压电ICSI方案,该方案可在2至4小时内完成。该方案是多种应用的基本前奏,包括核移植克隆、精子细胞注射、囊胚注射、mII转基因,以及简化灵长类动物和家畜的显微操作。此外,压电ICSI可用于从“死”(无运动能力)精子中获得后代,从而实现用于小鼠品系保存和运输的简单精子冷冻方案。