Bhartiya Deepa, Anand Sandhya, Parte Seema
Stem Cell Biology Department, National Institute for Research in Reproductive Health, JM Street, Parel, Mumbai, 400 012, India.
J Ovarian Res. 2015 Nov 17;8:75. doi: 10.1186/s13048-015-0199-2.
Infertility is an undesirable side effect and gonadal tissue banking is advocated in young cancer patients who are unable to preserve embryos or gametes prior to oncotherapy to achieve biological parenthood later on. Banking gonadal tissue is challenging and protocols to mature gametes in vitro are not yet clinically established. Transplanting ovarian cortical tissue at hetero-or orthotopic sites in women and bone marrow transplantation (BMT) in both men and women has resulted in spontaneous recovery of fertility, pregnancy and live births. Various studies in humans and mice suggest that genetic origin of offspring after BMT is similar to transplanted patient and not the donor. Thus the source of oocytes/sperm which result in spontaneous pregnancies still remains contentious.
Very small embryonic-like stem cells (VSELs) have been reported in adult human testis and ovary, in azoospermic testicular biopsies from survivors of childhood cancer and also in women with premature ovarian failure and menopause. VSELs survive chemotherapy because of their quiescent nature and can be detected in chemoablated mice gonads at protein and mRNA level and also by flow cytometry. Surviving VSELs spontaneously differentiate into oocyte-like structures and sperm when inhibitory factors are overcome in vitro. Transplantation of mesenchymal cells (isolated from different sources) has led to regeneration of chemoablated mouse gonads and also live births. Spermatogenesis is also restored from endogenous stem cells on inter-tubular transplantation of Sertoli cells in chemoablated mouse testis.
Endogenous VSELs (which survive oncotherapy) can possibly regenerate non-functional gonads in cancer survivors when exposed to a healthy niche in vitro or in vivo (by way of transplanting mesenchymal cells which secrete trophic factors required for endogenous VSELs to differentiate into gametes). Presence of VSELs can also explain spontaneous pregnancies after BMT and cortical tissue transplantation (at heterotopic or orthotopic sites). This understanding once verified and accepted by the scientific community could obviate the need to remove whole ovary or testicular biopsy for cryopreservation prior to oncotherapy.
不孕是一种不良副作用,对于那些在接受肿瘤治疗前无法保存胚胎或配子、希望日后实现生育的年轻癌症患者,提倡进行性腺组织储存。储存性腺组织具有挑战性,且体外配子成熟方案尚未在临床上确立。在女性的异位或原位移植卵巢皮质组织以及在男性和女性中进行骨髓移植(BMT)均已导致生育能力自发恢复、怀孕及活产。人类和小鼠的各种研究表明,BMT后子代的遗传来源与移植患者相似,而非供体。因此,导致自然怀孕的卵母细胞/精子来源仍存在争议。
在成年人类睾丸和卵巢、儿童癌症幸存者的无精子症睾丸活检组织以及卵巢早衰和绝经女性中均已报道存在非常小的胚胎样干细胞(VSELs)。VSELs因其静止特性在化疗中存活,并且在化疗后的小鼠性腺中可通过蛋白质和mRNA水平以及流式细胞术检测到。当体外克服抑制因子时,存活的VSELs可自发分化为卵母细胞样结构和精子。间充质细胞(从不同来源分离)的移植已导致化疗后小鼠性腺再生以及活产。在化疗后的小鼠睾丸中,将支持细胞进行管间移植后,内源性干细胞也可恢复精子发生。
内源性VSELs(在肿瘤治疗中存活)在体外或体内暴露于健康微环境时(通过移植分泌内源性VSELs分化为配子所需营养因子的间充质细胞),有可能使癌症幸存者中无功能的性腺再生。VSELs的存在也可以解释BMT和皮质组织移植(异位或原位)后的自然怀孕。一旦这一认识得到科学界的验证和认可,可能无需在肿瘤治疗前切除整个卵巢或进行睾丸活检以进行冷冻保存。