Spermatids

精子细胞
  • 文章类型: Journal Article
    尽管辅助生殖技术取得了进展,不孕症仍然是世界范围内一贯的健康问题.精子化是成熟的精子细胞与支持的支持细胞分离并释放到小管腔中的过程。精子衰竭导致缺乏成熟的精子,如果不是偶尔,会导致无精子症,男性不育的主要原因。精子细胞通过顶端外质特化(aES)分化为精子,一个特定的睾丸,基于肌动蛋白的锚定连接仅限于Sertoli-精子细胞界面。aES有助于精子细胞在生精上皮中的运动,促进精子定位,并防止未成熟精子的释放。为了实现其功能,ES需要进行严格和及时的管制重组。即使aES的组成部分是部分已知的,调节aES的机制仍然难以捉摸。在这次审查中,我们提出了一个小GTP酶Rap1可以调节aES组装/重塑的模型。AES动态中关键参与者的表征,如Rap1,可以为发展预后开辟新的可能性,诊断,以及正在接受不育症治疗的男性患者的治疗方法,这可能导致确定男性避孕的新目标。
    Despite advances in assisted reproductive technologies, infertility remains a consistent health problem worldwide. Spermiation is the process through which mature spermatids detach from the supporting Sertoli cells and are released into the tubule lumen. Spermiation failure leads to lack of mature spermatozoa and, if not occasional, could result into azoospermia, major cause of male infertility in human population. Spermatids are led through their differentiation into spermatozoa by the apical ectoplasmic specialization (aES), a testis-specific, actin-based anchoring junction restricted to the Sertoli-spermatid interface. The aES helps spermatid movement across the seminiferous epithelium, promotes spermatid positioning, and prevents the release of immature spermatozoa. To accomplish its functions, aES needs to undergo tightly and timely regulated restructuring. Even if components of aES are partly known, the mechanism/s through which aES is regulated remains still elusive. In this review, we propose a model by which the small GTPase Rap1 could regulate aES assembly/remodelling. The characterization of key players in the dynamic of aES, such as Rap1, could open new possibility to develop prognostic, diagnostic, and therapeutic approaches for male patients under treatment for infertility as well as it could lead to the identification of new target for male contraception.
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  • 文章类型: Case Reports
    对Chianina牛(BTA)品种的常规细胞遗传学研究表明,在幼年的细胞中,存在比最大(BTA1)和最小(BTA29)染色体更长,更小的染色体,用于繁殖的长相正常的公牛。RBA显带和Ag-NOR技术的应用,以及使用FISH技术和两种BTA11(IL1B,ASS和LGB)和BTA21(SERPINA和D21S45)确定这两个异常染色体是BTA11和BTA21之间相互易位的产物。der(11)和der(21)均为C带阳性,受影响的染色体区域为rcp(11;21)(q28;q12)。这只年轻的公牛身体形态正常,包括外生殖器,睾酮的正常水平(如在对照中)和17β-雌二醇和孕酮的不可检测水平(如在对照中)。在发情的雄性和雌性都存在的情况下,动物从未表现出性欲。经过18个月的屠杀,组织学评估显示睾丸组织正常,精细管和附睾,但主要由精原细胞组成的增殖性差的生殖细胞,中间粗线质精母细胞和早期精子细胞,晚期精子细胞和精子非常罕见。
    Routine cytogenetic investigations of the Chianina cattle (BTA) breed revealed the presence of longer and smaller chromosomes than the largest (BTA1) and smallest (BTA29) chromosomes in the cells of a young, normal-looking bull used for reproduction. Application of both RBA-banding and Ag-NOR techniques, as well as the use of the FISH technique and specific molecular markers of both BTA11 (IL1B, ASS and LGB) and BTA21 (SERPINA and D21S45) established that these two abnormal chromosomes were the product of a reciprocal translocation between BTA11 and BTA21. Both der(11) and der(21) were C-band positive and the chromosome regions affected were rcp(11;21)(q28;q12). The young bull had a normal body conformation, including external genitalia, normal levels of testosterone (as in the control) and non-detectable levels of both 17 beta-estradiol and progesterone (as in the control). The animal never showed libido in the presence of both males and females in oestrus. After slaughter at 18 months, histological evaluation revealed normal organized testes, seminiferous tubules and epididymis but with poor proliferative germ cells consisting mainly of spermatogonia, middle pachytene spermatocytes and early spermatids with late spermatids and spermatozoa being very rare.
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  • 文章类型: Journal Article
    为了确定非梗阻性无精子症男性不孕症的减数分裂标准,在巴黎(法国)的男性部门组织了一项前瞻性和多中心的研究,罗马(意大利)和布达佩斯(匈牙利)。在117例非梗阻性无精子症男性中,核型正常且无Y染色体微缺失,对双侧双极睾丸活检进行了组织学和减数分裂研究。组织学上,40例患者(34%)出现精母细胞或精子细胞停滞,39例(33%),而其余患者(33%)未观察到减数分裂细胞。细胞遗传学,减数分裂数据只能从两个前组织学组中获得。共有44例患者(37.6%)观察到减数分裂异常,其中9例(7.7%)患有严重的I类和IIB类异常,19例(16.2%)患有IIC类环境相关减数分裂异常。这些结果为准确的临床管理提供了必要的线索。对于无减数分裂图的患者和I类和IIB类异常的患者,荷尔蒙刺激是虚幻的,应该直接提出精子礼物。应该向所有其他患者建议激素刺激,对于出现IIC类异常的患者,直接或在治疗睾丸微环境之后。在妊娠的情况下,产前染色体分析的遗传风险和可能性应清楚地暴露于所有IIA型病例中的所有夫妇,存在III或IV异常。该治疗策略已应用于我们系列中的所有患者。
    To identify meiotic criteria for infertility management in non-obstructive azoospermic men, a prospective and multicentric study was organized in Andrological Departments of Paris (France), Roma (Italy) and Budapest (Hungary). In 117 non-obstructive azoospermic men with normal karyotype and no Y-chromosome microdeletion, histology and meiotic studies on bilateral bipolar testicular biopsies were done. Histologically, 40 patients (34%) presented spermatocyte or spermatid arrest, 39 (33%) hypospermatogenesis whereas no meiotic cell could be observed in the remaining patients (33%). Cytogenetically, meiotic figures could only be obtained from the two first histological groups. Meiotic abnormalities were observed in a total of 44 patients (37.6%) including nine patients (7.7%) with severe class I and class IIB anomalies and 19 patients (16.2%) with class IIC environmentally linked meiotic abnormalities. These results provided essential clues for an accurate clinical management. For patients with no meiotic figures and patients with class I and class IIB anomalies, an hormonal stimulation is illusory and a sperm gift should be directly proposed. An hormonal stimulation should be proposed to all the other patients, either directly or following the treatment of the testicular microenvironment for the patients presenting class IIC anomalies. The genetic risk and possibility of prenatal chromosomal analysis in case of pregnancy should be clearly exposed to all the couples in all the cases where type IIA, III or IV anomalies are present. This therapeutical strategy has been applied to all the patients in our series.
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    文章类型: Case Reports
    这是在无精子症男性患者中成功治疗男性不育的报告。使用睾丸精子提取技术(TESE)并检索圆形细胞精子细胞。使用圆形细胞精子细胞注射技术(ROSI)进行体外受精。经腹腔镜将受精卵转入右输卵管,实现宫内妊娠。妊娠38周时进行剖宫产,产生体重2820g的健康男婴。随访2年后,孩子的身心发育正常。
    This is a report of a success in the treatment of male infertility in a case of azoospermic male patient. Testicular sperm extraction technique (TESE) was used and round cell spermatids were retrieved. In vitro fertilization was carried out using round cell spermatid injection technique (ROSI). The zygotes were laparoscopically transferred into right fallopian tube and intrauterine pregnancy was achieved. Cesarean delivery was performed at thirty eighth week of gestation yielding a healthy male infant weighing 2820 g. The child\'s physical and mental developments were normal after 2 years of follow-up.
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  • 文章类型: Journal Article
    众所周知,Diplozoon显示出一种特殊的生殖生物学:雌雄同体的成年人永久融合在一起,并且它们的生殖器导管进行交流。与所有其他精子表现出均匀的双鞭毛虫结构的单基因组相反,二倍体的精子是无尾藻。它是丝状的,由细胞质区域和细胞核区域组成。细胞质区域显示线粒体,一个发育良好的平滑内质网,和高达450纵向单线微管。微管显示它们之间的联系;从横截面看,它们排列为行或多边形。精子核区域包含被皮质纵向微管包围的核。精子发生没有分化区域,在所有其他寄生平台中发现的典型结构。Diplozoon是在寄生的Platyhelminthes中发现的首例无胶精子。不典型的精子结构与系统发育无关,但与非典型的生殖生物学密切相关。
    Diplozoon is known to display an exceptional biology of reproduction: the hermaphroditic adults are permanently fused together and their genital ducts communicate. In contrast to all other polyopisthocotylean monogeneans in which the spermatozoa show an homogeneous biflagellate structure, the spermatozoon of Diplozoon is aflagellate. It is filiform, and composed of a cytoplasmic region and a nuclear region. The cytoplasmic region exhibits mitochondria, a well-developed smooth endoplasmic reticulum, and up to 450 longitudinal singlet microtubules. The microtubules show links between them; seen in cross section, they are arranged as rows or polygons. The spermatozoon nuclear region contains the nucleus surrounded by cortical longitudinal microtubules. The spermiogenesis shows no zone of differentiation, a typical structure found in all other parasitic Platyhelminthes. Diplozoon is the first case of aflagellate spermatozoon found in the parasitic Platyhelminthes. The atypical sperm structure is not linked with phylogeny, but is well correlated with the atypical biology of reproduction.
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  • 文章类型: Journal Article
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