Laffafian I, Hallett M B
Molecular Signaling Group, University Department of Surgery, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, Wales.
Biophys J. 1998 Nov;75(5):2558-63. doi: 10.1016/S0006-3495(98)77700-8.
The microinjection of synthetic molecules, proteins, and nucleic acids into the cytosol of living cells is a powerful technique in cell biology. However, the insertion of a glass micropipette into the cell is a potentially damaging event, which presents significant problems, especially for small mammalian cells (spherical diameter = 2-15 micron), especially if they are only loosely adherent. The current technique is therefore limited to cells that are both sufficiently large or robust and firmly attached to a substrate. We describe here a modification of the standard technique that overcomes some of the problems associated with conventional microinjection but that does not involve the insertion of a micropipette deep into the cell cytoplasm. Instead, this method depends on lipid fusion at the micropipette tip to form a continuous but temporary conductance pathway between the interiors of the micropipette and cell. This technique thus also provides a novel method of transferring lipids and lipid-associated molecules to the plasma membrane of cells.
将合成分子、蛋白质和核酸显微注射到活细胞的细胞质中是细胞生物学中的一项强大技术。然而,将玻璃微吸管插入细胞是一个潜在的损伤事件,会带来重大问题,尤其是对于小型哺乳动物细胞(球形直径 = 2 - 15微米),特别是如果它们只是松散附着的情况下。因此,当前技术仅限于足够大或强壮且牢固附着于基质的细胞。我们在此描述了一种对标准技术的改进,该改进克服了与传统显微注射相关的一些问题,且不涉及将微吸管深入插入细胞质中。相反,此方法依赖于微吸管尖端的脂质融合,以在微吸管内部和细胞之间形成连续但临时的导电通路。因此,该技术还提供了一种将脂质和脂质相关分子转移到细胞质膜的新方法。