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Cellular Therapy via Spermatogonial Stem Cells for Treating Impaired Spermatogenesis Non-Obstructive Azoospermia

机译:细胞疗法通过精牙科干细胞治疗损伤的精子发生非阻塞性​​血吸虫

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摘要

Male infertility is a major health problem affecting about 8–12% of couples worldwide. Spermatogenesis starts in the early fetus and completes after puberty, passing through different stages. Male infertility can result from primary or congenital, acquired, or idiopathic causes. The absence of sperm in semen, or azoospermia, results from non-obstructive causes (pretesticular and testicular), and post-testicular obstructive causes. Several medications such as antihypertensive drugs, antidepressants, chemotherapy, and radiotherapy could lead to impaired spermatogenesis and lead to a non-obstructive azoospermia. Spermatogonial stem cells (SSCs) are the basis for spermatogenesis and fertility in men. SSCs are characterized by their capacity to maintain the self-renewal process and differentiation into spermatozoa throughout the male reproductive life and transmit genetic information to the next generation. SSCs originate from gonocytes in the postnatal testis, which originate from long-lived primordial germ cells during embryonic development. The treatment of infertility in males has a poor prognosis. However, SSCs are viewed as a promising alternative for the regeneration of the impaired or damaged spermatogenesis. SSC transplantation is a promising technique for male infertility treatment and restoration of spermatogenesis in the case of degenerative diseases such as cancer, radiotherapy, and chemotherapy. The process involves isolation of SSCs and cryopreservation from a testicular biopsy before starting cancer treatment, followed by intra-testicular stem cell transplantation. In general, treatment for male infertility, even with SSC transplantation, still has several obstacles. The efficiency of cryopreservation, exclusion of malignant cells contamination in cancer patients, and socio-cultural attitudes remain major challenges to the wider application of SSCs as alternatives. Furthermore, there are limitations in experience and knowledge regarding cryopreservation of SSCs. However, the level of infrastructure or availability of regulatory approval to process and preserve testicular tissue makes them tangible and accurate therapy options for male infertility caused by non-obstructive azoospermia, though in their infancy, at least to date.
机译:男性不育症是影响全球的夫妇约8-12%的主要健康问题。精子发生开始于青春期后的早期胎儿和完成,通过不同的阶段。男性不育可以导致从原发性或先天性的,获得的,或特发性的原因。在精液,无精子症或从非梗阻性原因(pretesticular和睾丸),和睾丸后阻塞性原因的结果不存在精子。一些药物,如降压药,抗抑郁药,化疗和放疗可能导致生精障碍,并导致非梗阻性无精子症。精原干细胞(SSCS)是男性精子发生和生育能力的基础。共享服务中心是由他们保持整个男性生殖生活和传输遗传信息传给下一代的自我更新过程,并分化成精子的能力特点。精原干细胞在出生后睾丸的生殖母细胞,其胚胎发育过程中,从长寿命的原始生殖细胞起源起源。不孕不育的男性治疗预后差。然而,精原干细胞被视为对受损的或受损的精子发生的再生有前途的替代。 SSC移植是男性不育治疗和精子发生的恢复在退化性疾病,如癌症,放射疗法和化学疗法的情况下,有前途的技术。该过程涉及从睾丸活检SSC的分离和冷冻保存开始癌症治疗,随后帧内睾丸干细胞移植之前。在一般情况下,治疗男性不育症,甚至与移植SSC,仍然存在一些障碍。冷冻保存的效率,在癌症患者恶性细胞污染的排斥,以及社会文化的态度仍然是精原干细胞作为替代品的广泛应用主要挑战。此外,也有经验和知识的局限性有关精原干细胞冷冻保存。然而,基础设施和监管部门的批准过程的可用性和保护睾丸组织水平,使他们所造成的非梗阻性无精子男​​性不育有形的和准确的治疗方案,虽然处于起步阶段,至少到目前为止。

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