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Sperm preparation: state-of-the-art—physiological aspects and application of advanced sperm preparation methods

机译:精子制备:最新的生理学方面和先进的精子制备方法的应用

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摘要

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.
机译:对于辅助生殖技术(ART),开发了许多技术来分离能够使卵母细胞受精的精子。尽管早期方法仅专注于分离活的,能活动的精子,但随着ART的进展,尤其是胞浆内精子注射(ICSI),显然这些参数不足以鉴定最合适的受精精子。常规的精子制备技术,如游泳,密度梯度离心和玻璃棉过滤,效率不足以产生没有DNA损伤的精子群体,因为这些技术不是生理性的,并且没有模拟严格的精子选择过程。女性生殖道。这些过程仅允许数千万个雄性生殖细胞与卵母细胞融合。女性生殖道中精子选择的部位是子宫颈,子宫,输卵管交界处,输卵管,卵丘和透明带。较新的精子制备策略基于:(i)通过“活动精子细胞器形态学检查(MSOME)”进行形态学评估;(ii)电荷; (iii)精细胞的分子结合特性。基于电荷的分离方法利用了精子对试管表面的粘附或在电泳中进行分离,而分子结合技术则使用膜联蛋白V或透明质酸(HA)作为底物。此类技术包括磁活化细胞分选,膜联蛋白V活化玻璃棉过滤,流式细胞术和从HA涂层培养皿和含HA的培养基中提取用于ICSI(PICSI)的精子。未来的发展可能包括拉曼光谱,共聚焦光吸收和散射光谱显微镜以及偏振显微镜。

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