Kobayashi Hideyuki, Nagao Koichi, Nakajima Koichi, Miura Kazukiyo, Ishii Nobuhisa
Department of Urology Toho University School of Medicine 6-11-1 Omori-Nishi, Ota-ku 143-8541 Tokyo Japan.
Reprod Med Biol. 2009 Apr 28;8(2):71-77. doi: 10.1007/s12522-009-0014-0. eCollection 2009 Jun.
Spermatogonial stem cells (SSCs) are self-renewing cells whose progeny are committed to differentiate into spermatozoa; this is a life-long process in male mammals. There are several methods for obtaining enriched populations of mouse SSCs, and immunological separation using surface antigens is a commonly used technique. The study of human SSCs is much less advanced.
We used biopsied human testicular tissues [obstructive azoospermia patients ( = 5) and patients who underwent a testis biopsy as part of an evaluation for infertility ( = 7)] to obtain Thy-1 cells. Thy-1-a glycosyl phosphatidylinositol-anchored surface antigen-is a marker uniquely expressed on SSCs that is used to isolate SSC-enriched cell populations in mice. The Thy-1 cells from human testicular tissues were cultured in a basic system consisting of serum-free medium and mitotically inactivated STO (SIM mouse embryo-derived thioguanine- and ouabain-resistant) cell feeders with added growth factors: glial cell line-derived neurotrophic factor (GDNF), basic fibroblast growth factor (bFGF), and GDNF-family receptor α1 (GFRα-1).
The Thy-1 cells were maintained in vitro using this system for 1 week. The Thy-1 cells expressed OCT3/4 and alkaline phosphatase, like mouse SSCs. They also expressed NANOG. Thy-1 cells injected into nude mice did not cause tumor formation over a period of at least 6 months.
These results support the possibility that the Thy-1 cell population included human SSCs, and that Thy-1 may be a marker for human SSCs.
精原干细胞(SSCs)是具有自我更新能力的细胞,其后代会分化为精子;这是雄性哺乳动物一生的过程。有几种方法可用于获得富集的小鼠精原干细胞群体,利用表面抗原进行免疫分离是一种常用技术。人类精原干细胞的研究则相对滞后得多。
我们使用活检的人类睾丸组织[梗阻性无精子症患者(n = 5)和作为不育评估一部分接受睾丸活检的患者(n = 7)]来获取Thy-1细胞。Thy-1是一种糖基磷脂酰肌醇锚定的表面抗原,是精原干细胞上独特表达的标志物,用于在小鼠中分离富集精原干细胞的细胞群体。将来自人类睾丸组织的Thy-1细胞在一个基本体系中培养,该体系由无血清培养基和有丝分裂失活的STO(SIM小鼠胚胎来源的硫代鸟嘌呤和哇巴因抗性)细胞饲养层以及添加的生长因子组成:胶质细胞源性神经营养因子(GDNF)、碱性成纤维细胞生长因子(bFGF)和GDNF家族受体α1(GFRα-1)。
使用该体系,Thy-1细胞在体外维持了1周。Thy-1细胞像小鼠精原干细胞一样表达OCT3/4和碱性磷酸酶。它们也表达NANOG。注射到裸鼠体内的Thy-1细胞在至少6个月的时间内未导致肿瘤形成。
这些结果支持这样一种可能性,即Thy-1细胞群体中包含人类精原干细胞,并且Thy-1可能是人类精原干细胞的一个标志物。