Department of Medical Biosciences, University of the Western Cape, Bellville 7535, South Africa.
Asian J Androl. 2012 Mar;14(2):260-9. doi: 10.1038/aja.2011.133. Epub 2011 Dec 5.
For assisted reproduction technologies (ART), numerous techniques were developed to isolate spermatozoa capable of fertilizing oocytes. While early methodologies only focused on isolating viable, motile spermatozoa, with progress of ART, particularly intracytoplasmic sperm injection (ICSI), it became clear that these parameters are insufficient for the identification of the most suitable spermatozoon for fertilization. Conventional sperm preparation techniques, namely, swim-up, density gradient centrifugation and glass wool filtration, are not efficient enough to produce sperm populations free of DNA damage, because these techniques are not physiological and not modeled on the stringent sperm selection processes taking place in the female genital tract. These processes only allow one male germ cell out of tens of millions to fuse with the oocyte. Sites of sperm selection in the female genital tract are the cervix, uterus, uterotubal junction, oviduct, cumulus oophorus and the zona pellucida. Newer strategies of sperm preparation are founded on: (i) morphological assessment by means of 'motile sperm organelle morphological examination (MSOME)'; (ii) electrical charge; and (iii) molecular binding characteristics of the sperm cell. Whereas separation methods based on electrical charge take advantage of the sperm's adherence to a test tube surface or separate in an electrophoresis, molecular binding techniques use Annexin V or hyaluronic acid (HA) as substrates. Techniques in this category are magnet-activated cell sorting, Annexin V-activated glass wool filtration, flow cytometry and picked spermatozoa for ICSI (PICSI) from HA-coated dishes and HA-containing media. Future developments may include Raman microspectrometry, confocal light absorption and scattering spectroscopic microscopy and polarization microscopy.
对于辅助生殖技术(ART),已经开发了许多技术来分离能够受精卵母细胞的精子。虽然早期的方法学仅专注于分离有活力、有活力的精子,但随着 ART 的进展,特别是胞浆内单精子注射(ICSI),很明显,这些参数不足以识别最适合受精的精子。传统的精子制备技术,即泳动、密度梯度离心和玻璃纤维过滤,不足以产生无 DNA 损伤的精子群体,因为这些技术不是生理性的,也没有模拟女性生殖道中严格的精子选择过程。这些过程只允许数千万个男性生殖细胞中的一个与卵母细胞融合。女性生殖道中的精子选择部位是宫颈、子宫、子宫输卵管连接处、输卵管、卵丘和透明带。较新的精子制备策略基于:(i)通过“运动精子细胞器形态检查(MSOME)”进行形态评估;(ii)电荷;和(iii)精子细胞的分子结合特性。而基于电荷的分离方法利用精子附着在试管表面或在电泳中分离,分子结合技术则使用 Annexin V 或透明质酸(HA)作为底物。该类技术包括磁激活细胞分选、 Annexin V 激活的玻璃纤维过滤、流式细胞术和从 HA 涂层培养皿中挑选用于 ICSI(PICSI)的精子和含有 HA 的培养基。未来的发展可能包括拉曼微光谱学、共聚焦光吸收和散射光谱显微镜和偏振显微镜。