Chojnacka-Puchta L, Kasperczyk K, Płucienniczak G, Sawicka D, Bednarczyk M
Institute of Biotechnology and Antibiotics, Staroscinska 5, 02-516 Warszawa, Poland.
Pol J Vet Sci. 2012;15(1):181-8. doi: 10.2478/v10181-011-0132-6.
The transgenic chicken has great potential as a bioreactor for the production of valuable pharmaceutical proteins, notably in the oviduct/egg. Whereas conventional transgenic approaches have significant limitations in this species, an alternative approach employing primordial germ cells (PGCs), the progenitor cells to ova and spermatozoa, has now been successfully applied to the insertion of exogenous genes into birds. Recent developments in manipulating avian embryos make it possible to produce germline chimeras derived from transferred PGCs. In this review we describe the migration pathway of chicken PGCs during early development. We then summarize different methods for the isolation of PGCs and the diversity of techniques used to introduce genes into these cells. Finally, we describe an in vitro assay for testing tissue-specific vectors designed to express heterologous proteins in transgenic chickens.
转基因鸡作为生产有价值药用蛋白质的生物反应器具有巨大潜力,尤其是在输卵管/鸡蛋中。尽管传统的转基因方法在该物种中存在重大局限性,但一种利用原始生殖细胞(PGCs)(卵子和精子的祖细胞)的替代方法现已成功应用于将外源基因插入鸟类。操纵禽类胚胎的最新进展使得产生源自转移PGCs的种系嵌合体成为可能。在这篇综述中,我们描述了鸡PGCs在早期发育过程中的迁移途径。然后,我们总结了分离PGCs的不同方法以及用于将基因导入这些细胞的技术多样性。最后,我们描述了一种体外试验,用于测试旨在在转基因鸡中表达异源蛋白质的组织特异性载体。