Abdelaal Nesma E, Tanga Bereket Molla, Abdelgawad Mai, Allam Sahar, Fathi Mostafa, Saadeldin Islam M, Bang Seonggyu, Cho Jongki
Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Universite Paris-Saclay/Île-de-France, 91198 Gif-sur-Yvette, France.
College of Veterinary Medicine, Chungnam National University, Daejeon 34134, Korea.
Cells. 2021 Jul 14;10(7):1779. doi: 10.3390/cells10071779.
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.
男性不育是一个重大的健康问题,影响着全球约8%至12%的夫妇。精子发生始于胎儿早期,在青春期后完成,历经不同阶段。男性不育可由原发性或先天性、后天性或特发性原因引起。精液中无精子,即无精子症,是由非梗阻性原因(睾丸前和睾丸性)以及睾丸后梗阻性原因导致的。几种药物,如抗高血压药、抗抑郁药、化疗药物和放疗,可能导致精子发生受损并引发非梗阻性无精子症。精原干细胞(SSCs)是男性精子发生和生育能力的基础。精原干细胞的特点是在男性整个生殖生命过程中能够维持自我更新过程并分化为精子,同时将遗传信息传递给下一代。精原干细胞起源于出生后睾丸中的生殖母细胞,而生殖母细胞在胚胎发育期间起源于长寿的原始生殖细胞。男性不育的治疗预后不佳。然而,精原干细胞被视为受损或损伤的精子发生再生的有前景的替代方案。精原干细胞移植是一种有前景的技术,可用于治疗男性不育以及在癌症、放疗和化疗等退行性疾病情况下恢复精子发生。该过程包括在开始癌症治疗前从睾丸活检中分离精原干细胞并进行冷冻保存,随后进行睾丸内干细胞移植。一般来说,即使采用精原干细胞移植治疗男性不育,仍然存在一些障碍。冷冻保存的效率、癌症患者中恶性细胞污染的排除以及社会文化态度仍然是精原干细胞作为替代方案更广泛应用的主要挑战。此外,关于精原干细胞冷冻保存的经验和知识存在局限性。然而,处理和保存睾丸组织的基础设施水平或监管批准的可用性使它们成为治疗非梗阻性无精子症所致男性不育的切实可行且准确的治疗选择,尽管至少到目前为止它们仍处于起步阶段。