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! d5 \" I* _8 H4 ^俺的理解: 在分离和长期培养人ESC和IPS cell 的过程中,消除动物材料,比如动物血清 。这样一来胚胎干细胞在临床应用方面 就会更加安全, 会降低免疫排斥反应 ,消除动物材料所带来的 非人类的病原体。
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) X2 m! i1 |# ?具体参考:uman embryonic stem cells (hESCs) hold great promise for future clinical cell therapies in the fields of, for example, diabetes, cardiac infarction, and neurodegenerative diseases, because of their unique potential to differentiate into all cell types found in the human body. In addition, it has recently been revealed that hESCs and their differentiated derivatives are less susceptible to immune rejection than adult cells [1], which is encouraging news for future clinical application. However, the majority of hESC lines available to date have been directly or indirectly exposed to animal material during their derivation and/or propagation in vitro. Transplanting xeno-contaminated hESCs to patients will increase the risk of graft rejection [2] and transfer of nonhuman pathogens, suggesting that the existing hESC lines are unsuitable for clinical applications. Closer inspection of previous attempts to establish xeno-free hESC lines reveals, in each case, that not all animal products had been replaced. For example, several recent hESC derivation reports [3, [4]–5] used Knock-Out serum replacement (SR), which contains animal protein and is a source of nonhuman sialic acid [2]. Although Richards et al. [6] used human serum (HS) and human feeder cells, and Ludwig et al. [7] recently presented the derivation of two human ES cell lines (WA15 and WA16) in a chemically defined cell culture system, they both used immunosurgery to isolate the inner cell mass (ICM). Immunosurgery is a method commonly used to remove the outer trophectoderm epithelial cell layer from the blastocyst by incubation in polyclonal rabbit anti-human whole-serum antibodies and guinea pig complement. Consequently, although these culture systems may be free of animal products, the derivation procedure is not, and therefore, these hESC lines should be considered potentially xeno-contaminated. |
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