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Unique Sertoli cell adaptations support enhanced spermatogenesis in chickens
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作者 Gaoqing Xu Zhuoxuan Gu +8 位作者 Ziming Wang Jing Zhao He Ding Hongyu Liu Yi Fang Xin Ma Jing Guo Wenfa Lyu Jun Wang 《Journal of Animal Science and Biotechnology》 2026年第1期192-212,共21页
Background The cellular basis of testicular development and spermatogenesis for the extreme sperm density in chickens(100-fold higher than mammals)remains poorly defined.A comprehensive understanding of the molecular ... Background The cellular basis of testicular development and spermatogenesis for the extreme sperm density in chickens(100-fold higher than mammals)remains poorly defined.A comprehensive understanding of the molecular characteristics driving poultry testicular development is crucial for explaining this enhanced spermatogenic capacity.Results Here,we first established a single-cell transcriptome profile of chicken testes from hatching to maturity,identifying the dynamic transcriptional characteristics of germ cell fate transition and exploring the developmental characteristics of Sertoli cells and Leydig cells.Multi-species comparisons revealed a higher proportion of germ cells and the unique adaptations of Sertoli cells in chicken testes.Most importantly,our results demonstrated that Sertoli cells dominated in somatic composition of mature chicken testes,and proliferating Sertoli cells persisted in chicken testes even after sexual maturity,while no proliferating Sertoli cells in mammals.We also found a richer interaction network between chicken testicular cells,especially the specific activation of Sertoli cell interaction signals,such as TGF-β,BMP,EGF,and activin.These adaptations of Sertoli cells may support the spermatogenic superiority in chickens.Additionally,our results indicated that cAMP responsive element binding protein 5(CREB5)played a crucial role in maintaining the maturation and function of chicken Sertoli cells,and circadian rhythm promoted testosterone secretion and the development of Leydig cells.Conclusion Our study revealed that the sustained proliferative capacity of Sertoli cells,their enriched signaling network,and the regulatory roles of CREB5 and circadian rhythms collectively represented unique testicular adaptations in chickens.These findings may hold extraordinary significance in understanding the molecular characteristics of poultry testicular development,and provide a plausible framework for explaining enhanced spermatogenesis in poultry. 展开更多
关键词 Chicken testes Leydig cells Sertoli cells Single-cell RNA sequencing spermatogenesis
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Microfluidic systems in testicular in vitro culture: a powerful model tool for spermatogenesis and reprotoxicity studies
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作者 Botho Maximilian Schneider Hande Irem Hamurcu +1 位作者 Andrea Salzbrunn Kathrein von Kopylow 《Asian Journal of Andrology》 2025年第6期659-668,共10页
As prepubertal boys do not yet produce spermatozoa,they cannot rely on sperm cryopreservation for fertility preservation before gonadotoxic therapy,such as high-dose alkylating agents or radiotherapy in the case of ch... As prepubertal boys do not yet produce spermatozoa,they cannot rely on sperm cryopreservation for fertility preservation before gonadotoxic therapy,such as high-dose alkylating agents or radiotherapy in the case of childhood cancers.According to the current guidelines,cryopreservation of testicular biopsies containing spermatogonial stem cells(SSCs)may be proposed to high-risk patients for potential later therapeutic use to fulfill the patients’wish for a biological child.One promising technique for human in vitro spermatogenesis and in vitro propagation of human SSCs is microfluidic(MF)culture,in which cells or tissues are subjected to a continuous flow of medium.This provides exact control over such parameters as nutrient content and gradients,as well as the removal of waste metabolites.While MF has been shown to maintain tissues and cell populations of organs for longer than conventional in vitro culture techniques,it has not been widely used for testicular in vitro culture.MF could advance human testicular in vitro culture and is also applicable to reprotoxicity studies.This review summarizes the findings and achievements of testis-on-chip(ToC)setups to date and discusses the benefits and limitations of these for spermatogenesis in vitro and toxicity assessment. 展开更多
关键词 in vitro spermatogenesis MICROFLUIDICS reprotoxicity spermatogonial stem cells TESTIS testis-on-chip
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A convenient research strategy for functional verification of epigenetic regulators during spermatogenesis
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作者 Shan Li Ying Yuan +9 位作者 Ke-Yu Zhang Yi-Dan Guo Lu-Tong Wang Xiao-Yuan Zhang Shu Zhang Qi Yan Rong Zhang Jie Chen Feng-Tang Yang Jing-Rui Li 《Asian Journal of Andrology》 2025年第2期261-267,共7页
Spermatogenesis is a fundamental process that requires a tightly controlled epigenetic event in spermatogonial stem cells(SSCs).The mechanisms underlying the transition from SSCs to sperm are largely unknown.Most stud... Spermatogenesis is a fundamental process that requires a tightly controlled epigenetic event in spermatogonial stem cells(SSCs).The mechanisms underlying the transition from SSCs to sperm are largely unknown.Most studies utilize gene knockout mice to explain the mechanisms.However,the production of genetically engineered mice is costly and time-consuming.In this study,we presented a convenient research strategy using an RNA interference(RNAi)and testicular transplantation approach.Histone H3 lysine 9(H3K9)methylation was dynamically regulated during spermatogenesis.As Jumonji domain-containing protein 1A(JMJD1A)and Jumonji domain-containing protein 2C(JMJD2C)demethylases catalyze histone H3 lysine 9 dimethylation(H3K9me2),we firstly analyzed the expression profile of the two demethylases and then investigated their function.Using the convenient research strategy,we showed that normal spermatogenesis is disrupted due to the downregulated expression of both demethylases.These results suggest that this strategy might be a simple and alternative approach for analyzing spermatogenesis relative to the gene knockout mice strategy. 展开更多
关键词 JMJD1A JMJD2C H3K9me2 spermatogenesis spermatogonial stem cell
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Male Reproductive System and Spermatogenesis in Homoptera(Insecta:Hemiptera) 被引量:9
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作者 田润刚 袁锋 张雅林 《Entomotaxonomia》 CSCD 北大核心 2006年第4期241-253,共13页
Morphology of the male reproductive system, chromosome behaviors during meiosis and spem tail structures in Homoptera and Heteroptera are compared in this paper. The sheathed testis is found in Fulgoroidea and Heterop... Morphology of the male reproductive system, chromosome behaviors during meiosis and spem tail structures in Homoptera and Heteroptera are compared in this paper. The sheathed testis is found in Fulgoroidea and Heteroptera, and unsheathed testis occurs in Cicadoidea, Cicadelloidea, Cercopoidea, Membracoidea, Psyloidea, Aphidoidea, Aleyrodoidea and Coccoidea. The testis also can be divide into three types by the shape of testicular follicles. The sphere-shaped type is found in Cicadoidea, Cicadelloidea, Cercopoidea, Membracoidea, Aphidoidea and Aleyrodoidea, the tube-shaped type observed in Fulgoroidea, Psyloidea and Coccoidea, and the lamella-shaped type represented by Heteroptera. It is suggested the unsheathed testis may be the primitive type in Homoptera. Meiosis can be divided into 6 type at least, i.e. 1) Cicadoid type; 2) Fulgoroid type; 3) Psyloid type; 4) Aphidoid type; 5) Aleyrodoid type; and 6) Coccoid type. At least four groups exhibit a diffuse stage during meiosis prophase l, they are Psyloidea, Fulgoroidea, Coccoidea and Heteroptera. Sperm tail structures are similar to those reported from other insects with a typical 9+9+2 axoneme except that in Aleyrodoidea and Coccoidea whose sperm tail is degenerated. 展开更多
关键词 HEMIPTERA HOMOPTERA reproductive system spermatogenesis MEIOSIS sperm structure
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淫羊藿苷通过调钙质改善运动性疲劳模型小鼠精子发生的作用及机制
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作者 唐琨洋 萧闵 +4 位作者 江晓翠 陶晓雪 邹悦 赵纯纯 方志鹏 《中国实验方剂学杂志》 北大核心 2026年第8期117-127,共11页
目的:研究淫羊藿苷对运动性疲劳影响小鼠精子发生过程的作用并探讨有关的机制。方法:将ICR雄性小鼠进行游泳筛选并随机分为正常组,模型组,维生素C组,淫羊藿苷低、中、高剂量组,淫羊藿苷中剂量+N-硝基-L-精氨酸甲酯(L-NAME)组,每组10只... 目的:研究淫羊藿苷对运动性疲劳影响小鼠精子发生过程的作用并探讨有关的机制。方法:将ICR雄性小鼠进行游泳筛选并随机分为正常组,模型组,维生素C组,淫羊藿苷低、中、高剂量组,淫羊藿苷中剂量+N-硝基-L-精氨酸甲酯(L-NAME)组,每组10只。除正常组外各组通过负重游泳训练建立运动性疲劳模型。负重训练前2周不进行灌胃处理,第3~4周淫羊藿苷低、中、高剂量组分别给予0.03、0.06、0.12 g·kg^(-1)淫羊藿苷灌胃,维生素C组给予0.2 g·kg^(-1)维生素C灌胃,LNAME组给予0.06 g·kg^(-1)淫羊藿苷灌胃和0.01 g·kg^(-1) L-NAMA腹腔注射,正常组和模型组灌服等量的生理盐水。实验结束后,记录各组小鼠体质量、末次力竭游泳时间;试剂盒检测各组小鼠血清尿素氮(BUN)、乳酸(LA)、乳酸脱氢酶(LDH)、丙二醛(MDA)、睾丸睾酮(T)、睾丸Ca^(2+)/Mg^(2+)-ATP酶(微量法)、睾丸环磷酸鸟苷(cGMP)水平和流式细胞术检测精子CD46水平,苏木素-伊红(HE)染色法观察睾丸生精小管并进行睾丸生精功能评分(TMS)评分;蛋白免疫印迹法(Western blot)检测睾丸调钙质(RGN,SMP30)、环磷酸鸟苷依赖性蛋白激酶1(PKG)、环磷酸鸟苷依赖性蛋白激酶锚定蛋白(GKAP1)的蛋白表达;免疫荧光法(IF)检测睾丸Regucalcin的表达;显微镜下观察小鼠附睾精子质量;免疫组化(IHC)观察睾丸生精小管视黄酸刺激8(STRA8)、突触复合体蛋白3(SCP3)、过渡蛋白1(TNP1)荧光染色切片。结果:与正常组比较,模型组小鼠体质量下降、游泳力竭时间显著降低(P<0.01),疲劳标志物LA、LDH、BUN和脂质过氧化产物MDA水平显著升高(P<0.01),睾丸组织RGN、PKG、GKAP1、睾酮、Ca^(2+)/Mg^(2+)-ATP酶、cGMP水平显著下降(P<0.01),精子活力降低、精子数量减少、TMS评分下降,STRA8、SCP3、TNP1表达减少;与模型组比较,淫羊藿苷高剂量组游泳力竭时间显著增加(P<0.01),LA、LDH、BUN、MDA水平显著下降(P<0.01),SOD水平显著升高(P<0.01),睾丸组织RGN、PKG、GKAP1、睾酮、Ca^(2+)/Mg^(2+)-ATP酶、cGMP水平显著升高(P<0.01),精子活力升高、精子数量增加、TMS评分上升,STRA8、SCP3、TNP1表达增多;与L-NAME组比较,淫羊藿苷中剂量组睾丸组织STRA8、SCP3、TNP1表达显著增加(P<0.01),cGMP、GKAP1水平显著升高(P<0.01)。结论:运动性疲劳使得小鼠RGN和cGMP/PKG/GKAP1信号通路蛋白表达减少,并经由这一途径导致小鼠精子发生出现异常,影响生殖功能;淫羊藿苷通过促进RGN和cGMP/PKG/GKAP1信号通路蛋白表达进而改善运动性疲劳小鼠精子发生障碍,缓解运动性疲劳对生殖系统的损伤。 展开更多
关键词 运动性疲劳 精子发生 淫羊藿苷 调钙质
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TEKT3在高黎贡山猪睾丸发育中的表达特征与功能调控
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作者 周君蘭 霍海龙 +6 位作者 郭一鸣 牛一范 文飞滴 赵桂英 和胜 和塍 霍金龙 《河北农业大学学报》 北大核心 2026年第1期77-85,130,共10页
本研究旨在解析高黎贡山猪TEKT3(Tektin 3)的序列特征、分子结构及在睾丸发育中的表达调控情况,探究其在精子发生中的潜在功能。基于高黎贡山猪睾丸转录组测序数据,分析TEKT3的表达水平,并构建多物种系统进化树和蛋白互作网络。结果发现... 本研究旨在解析高黎贡山猪TEKT3(Tektin 3)的序列特征、分子结构及在睾丸发育中的表达调控情况,探究其在精子发生中的潜在功能。基于高黎贡山猪睾丸转录组测序数据,分析TEKT3的表达水平,并构建多物种系统进化树和蛋白互作网络。结果发现,TEKT3基因位于猪的12号染色体,含8个外显子,编码490个氨基酸。进化分析表明TEKT3在哺乳动物中高度保守,与单峰驼亲缘关系比较近。ceRNA网络分析发现sscmiR-125a、ssc-miR-125b和ssc-miR-10384靶向调控TEKT3,并与lncRNA竞争性结合ssc-miR-10384。KEGG富集分析和GO功能注释发现,该基因主要涉及微管稳定性和精子鞭毛运动等。互作蛋白网络提示TEKT3与EFCAB6、CCDC173等蛋白存在互作关系。组织发育表达谱显示TEKT3在睾丸中表达量随性成熟显著上调。免疫荧光(IF)定位显示TEKT3在睾丸组织及精子不同发育阶段的细胞分布,主要定位于精细胞与精子中。本研究揭示了高黎贡山猪TEKT3基因的分子特征及调控网络,为其在精子发生中的功能研究提供了理论基础。 展开更多
关键词 高黎贡山猪(Gaoligongshan pig) TEKT3 转录调控 精子发生
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基于microRNA与生物信息学筛选非梗阻性无精子症的生物标志物
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作者 李志宏 陈淼琪 +10 位作者 袁晓珺 黄华君 黄琬婷 周飘雁 曾晨 冯许诺 杨洛瑶 黄树强 谭翠钰 陈彩蓉 颜秋霞 《遗传》 北大核心 2026年第3期301-312,共12页
microRNA(miRNA)在非梗阻性无精子症(non-obstructive azoospermia,NOA)的发生中发挥着重要作用,但目前仍缺乏对其调控靶基因表达介导NOA发生分子机制的研究。本研究从GEO数据库获取NOA相关的miRNA数据集,通过差异分析、加权基因共表达... microRNA(miRNA)在非梗阻性无精子症(non-obstructive azoospermia,NOA)的发生中发挥着重要作用,但目前仍缺乏对其调控靶基因表达介导NOA发生分子机制的研究。本研究从GEO数据库获取NOA相关的miRNA数据集,通过差异分析、加权基因共表达网络分析(weighted correlation network analysis,WGCNA)和LASSO回归筛选得到4个关键miRNA。基于miRDB数据库预测miRNA的靶点基因,与NOA转录组数据集的差异表达基因(differential expressed genes,DEGs)取交集,获得18个DEGs。精子发生评分模型显示18个DEGs总表达水平与精子发生评分呈显著正相关,证明上述DEGs可能与NOA的发生相关。将18个DEGs纳入机器学习,最终鉴定出4个最具有诊断价值的关键基因MGARP、FER1L5、SNX2和PAPOLB。在NOA小鼠模型中,MGARP与SNX2表达上调,而FER1L5与PAPOLB表达下调,与NOA数据集表达趋势一致。以上结果表明MGARP、FER1L5、SNX2和PAPOLB可作为NOA的新型标志物,为NOA的机制研究与临床诊断提供理论基础和实验依据。 展开更多
关键词 MIRNA 非梗阻性无精子症 精子发生 机器学习 生物信息学
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基于睾丸组织共培养体系的Ddit3-Trib3-Akt信号通路与大鼠精子发生相关性的研究
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作者 李妍 刘珊珊 +4 位作者 高林 孔令怡 云霞 张岩 刘陶迪 《安徽医科大学学报》 北大核心 2026年第1期91-97,共7页
目的通过构建睾丸体外共培养体系来验证Ddit3-Trib3-Akt信号通路与大鼠精子发生相关。方法取20~25日龄雄性大鼠摘取睾丸组织块置于体外培养体系中,每隔2~3 d更换1次培养液。利用PCR验证各级生精细胞的标记基因。利用RNA干扰技术验证信... 目的通过构建睾丸体外共培养体系来验证Ddit3-Trib3-Akt信号通路与大鼠精子发生相关。方法取20~25日龄雄性大鼠摘取睾丸组织块置于体外培养体系中,每隔2~3 d更换1次培养液。利用PCR验证各级生精细胞的标记基因。利用RNA干扰技术验证信号通路Ddit3-Trib3-Akt与大鼠精子发生的相关性。结果该共培养体系可在体外连续培养超过2.5月,PCR结果显示精原细胞、精母细胞和精子细胞特异标记基因均有表达。利用RNA干扰技术,分别抑制Ddit3和Trib3后,Trib3和Akt基因的RNA和蛋白表达变化证明Ddit3-Trib3-Akt信号通路在大鼠精子发生中存在。结论该培养体系能够短暂维持干细胞的增殖和分化,在简单的体系上同时实现了维持与稳定的精子发生。Ddit3-Trib3-Akt信号通路的成功验证也说明该培养体系可用于体外研究精子发生的可能分子机制。 展开更多
关键词 组织共培养体系 精子发生 Ddit3-Trib3-Akt信号通路 大鼠 RNA干扰
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精母细胞的胞质桥必不可少——遗传、发育教材中减数分裂配图的讨论
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作者 任翔 唐朝晖 《生物学教学》 北大核心 2026年第4期90-92,共3页
探讨了减数分裂过程中精细胞间胞质桥的发现历程及其结构功能,指出当前教材中普遍存在的图示偏差:将减数分裂产物描绘为独立细胞,而实际上它们通过胞质桥连接,以合胞体形式存在。这对理解发育学和遗传学基础概念具有重要意义。
关键词 减数分裂 胞质桥 精子发生 教材配图
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龟龄集通过调节血清葡萄糖-6-磷酸水平改善小鼠少弱精子症的机制研究
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作者 徐瑶 戈榭 +2 位作者 向伊健 冯雨明 姚兵 《生殖医学杂志》 2026年第3期356-363,共8页
目的探索龟龄集(GLJ)改善少弱精子症的相关机制。方法将72只8周龄C57BL/6J雄性小鼠随机分为对照组(CTL组)、奥硝唑模型组(Orn组)、不同浓度GLJ组(Orn+GLJ组)和不同浓度葡萄糖-6-磷酸(G6P)组(Orn+G6P组),检测各组小鼠附睾尾精子浓度和精... 目的探索龟龄集(GLJ)改善少弱精子症的相关机制。方法将72只8周龄C57BL/6J雄性小鼠随机分为对照组(CTL组)、奥硝唑模型组(Orn组)、不同浓度GLJ组(Orn+GLJ组)和不同浓度葡萄糖-6-磷酸(G6P)组(Orn+G6P组),检测各组小鼠附睾尾精子浓度和精子活力,ELISA法检测血清卵泡刺激素(FSH)、黄体生成素(LH)、抑制素B(INHB)、睾酮(T)水平,苏木精-伊红(HE)染色观察睾丸和附睾组织结构,免疫荧光分析各级生殖细胞的数量。另将SD大鼠分为空白组(Base组)、GLJ组(灌胃)、GLJ+3-溴丙酮酸(3-BP)组(GLJ+3-BP组,腹腔注射),检测各组大鼠血清中G6P浓度并取各组血清加入培养基,进行小鼠精原细胞系(GC1)、精母细胞系(GC2)和支持细胞系(TM4)培养,观察血清中G6P浓度对睾丸各细胞系的影响。结果与Orn组小鼠比较,Orn+GLJ组和Orn+G6P组小鼠的血清G6P含量均显著增加(P<0.05),血清中FSH、LH、INHB水平均得到显著改善(P<0.05),精子浓度和精子活力均显著升高(P<0.05),睾丸内的生殖细胞数量均显著增加(P<0.05)。细胞培养结果显示,与Base组相比,GLJ组的GC1、GC2、TM4的细胞活力显著上升(P<0.05),且TM4的ATP水平显著增加(P<0.05);与GLJ组比较,GLJ+3-BP组中改善效果被显著抑制(P<0.01)。结论GLJ可能通过升高血清中G6P水平,增强生精微环境中的细胞能量代谢活性,促进各级生殖细胞及支持细胞的活力,最终改善OA模型小鼠的精子发生功能。 展开更多
关键词 龟龄集 葡萄糖-6-磷酸 精子发生 少弱精子症
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成纤维细胞生长因子受体1杂合缺失损伤小鼠精子活力
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作者 李晨阳 李婷 +4 位作者 王曦 聂敏 伍学焱 茅江峰 韩钦 《基础医学与临床》 2026年第4期524-530,共7页
目的探究先天性低促性腺激素性性腺功能减退症(CHH)中成纤维细胞生长因子受体1(FGFR1)杂合缺失对生殖功能的作用。方法构建FGFR1杂合敲除小鼠模型(FGFR1^(+/-)),运用聚合酶链反应(PCR)与Sanger测序方法进行分析,验证目标外显子的敲除情... 目的探究先天性低促性腺激素性性腺功能减退症(CHH)中成纤维细胞生长因子受体1(FGFR1)杂合缺失对生殖功能的作用。方法构建FGFR1杂合敲除小鼠模型(FGFR1^(+/-)),运用聚合酶链反应(PCR)与Sanger测序方法进行分析,验证目标外显子的敲除情况。采用免疫组化与Western blot,对蛋白表达进行检测。对小鼠的生殖能力、生殖功能(精子浓度、活力、前进性)展开测定,测量小鼠的BMI、睾丸质量、睾丸体积,以及各类性激素水平(包括T、E2、AMH、FSH、LH和INH-B),并进行统计学分析。结果研究构建了FGFR1杂合敲除的小鼠模型,PCR测序结果显示小鼠FGFR1外显子4、5被成功敲除,Western blot与免疫组化结果显示FGFR1蛋白表达减少。与野生型(WT)相比,FGFR1^(+/-)小鼠的精子活力更差(P<0.001),前进精子数量更少(P<0.01)。与WT小鼠相比,FGFR1^(+/-)小鼠的INH-B水平略有升高(P<0.05)。结论FGFR1杂合缺失影响小鼠精子活力,为深入探究先天性低促性腺激素性性腺功能减退症生殖功能障碍的发病机制提供了关键依据。 展开更多
关键词 成纤维细胞生长因子受体1 精子发生 睾丸发育 先天性低促性腺激素性性腺功能减退症
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男性年龄相关的雄激素变化及其意义
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作者 韦妮妮 袁书凝 +1 位作者 杨晓玉 崔毓桂 《中华男科学杂志》 2026年第1期69-75,共7页
在男性不同年龄阶段,雄激素水平呈现独特变化规律。胎儿期较高水平的雄激素促进性别分化和男性生殖器官初始发育;青春期雄激素持续渐进分泌,推动第二性征发育和生殖系统成熟;成年期雄激素大量合成分泌,保障性功能和精子生成;步入中老年... 在男性不同年龄阶段,雄激素水平呈现独特变化规律。胎儿期较高水平的雄激素促进性别分化和男性生殖器官初始发育;青春期雄激素持续渐进分泌,推动第二性征发育和生殖系统成熟;成年期雄激素大量合成分泌,保障性功能和精子生成;步入中老年期,雄激素水平因睾丸微环境改变而持续降低,甚至发生迟发性性腺功能减退。不同时期雄激素水平特征性的生理性波动,是男性生殖系统发育、第二性征、生精功能、性功能的源动力,与肌肉骨骼、代谢、心血管系统均密切相关。雄激素补充/替代治疗和抗氧化剂治疗为解决雄激素不足提供了有效手段。本文阐述男性不同年龄阶段的雄激素变化及其生理意义,探讨雄激素缺乏的临床治疗方案及其新路径。 展开更多
关键词 雄激素 第二性征 性成熟 精子生成 雄激素不足
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Transcriptomic landscape of Marchantia polymorpha sexual organs at single-nucleus resolution
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作者 Yuying Zeng Yuqing Cai +10 位作者 Zhencheng Tu Jingyi Liao Xiayi Chen Xing Guo Sibo Wangg Linzhou Li Yan Xu Shanshan Dong Huanming Yang Tong Wei Yang Liu 《Journal of Genetics and Genomics》 2026年第1期58-74,共17页
Marchantia polymorpha,a model liverwort,provides a valuable system for investigating the evolution of plant sexual reproduction.To explore the cellular landscape of its reproductive structures,we generate a single-nuc... Marchantia polymorpha,a model liverwort,provides a valuable system for investigating the evolution of plant sexual reproduction.To explore the cellular landscape of its reproductive structures,we generate a single-nucleus transcriptomic atlas of the antheridiophore,archegoniophore,and sporophyte.Using singlenucleus RNA sequencing(snRNA-seq),we capture over 30,000 high-quality nuclei and identify distinct cel populations.In the male organ,we characterize stages of spermatogenesis from early antheridium cells to mature sperm,revealing dynamic transcriptional programs including cell cycle regulation,chromatin remodeling,and calcium signaling.In the female organ,we define cell types including archegonial layers and secondary central cells.Sporophyte clusters are annotated as spores,elaters,capsule wall,foot,and seta cells,with transcriptional signatures related to structural support,stress response,and reproductive functions.Cross-species analysis indicates that capsule wall cells in liverworts are similar to tapetum cells.Notably,foot cells exhibit high expression of genes involved in sporopollenin biosynthesis and signaling pathways,serving as a central hub that mediates communication between the maternal gametophyte and the developing sporophyte.This study provides a comprehensive cellular and molecular map of M.polymorpha reproductive organs and sporophyte,establishing a framework for investigating the development and evolution of sexual reproduction in early land plants. 展开更多
关键词 Marchantia polymorpha Single-nucleus RNA sequencing Reproductive organ spermatogenesis Sporopollenin biosynthesis Cross-species comparison
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Dissecting the development of bovine testicular tissue using spatial transcriptomics
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作者 Haoyan Jin Yuan Ma +5 位作者 Yaru Xie Shunkai Yang Xiaoxu Chen Nana Wang Lingkai Zhang Yun Ma 《Journal of Animal Science and Biotechnology》 2026年第2期749-767,共19页
Background Mammalian spermatogenesis is critical for the transmission of male genetic information,and singlecell sequencing technology can reveal its complex process.However,at present,there is no research on the dyna... Background Mammalian spermatogenesis is critical for the transmission of male genetic information,and singlecell sequencing technology can reveal its complex process.However,at present,there is no research on the dynamic transcription of bovine germ cell population.Results In this study,we used Stereo-seq to construct a spatial transcription map of bovine testicular tissue at two ages.Four germ cell groups and five somatic cell groups were determined,and functional enrichment characterized their different biological functions and the differences between calves and adult bulls.At the same time,we also defined the subpopulations of cells and marker genes,then,clarified the communications between germ cells.Conclusion Our study constructed a spatial transcription map of bovine testicular tissue for the first time,and systematically described the dynamic transcription changes during spermatogenesis.These data laid the foundation for the study of spermatogenesis in large mammals and elucidated the transcriptional dynamics underlying male germ cell development. 展开更多
关键词 BOVINE Spatial transcriptome spermatogenesis
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精子发生领域下支持细胞研究热点与趋势的文献计量学分析
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作者 陈豪斌 刘晏平 +3 位作者 郭红梅 徐锦江 王智瀚 王权胜 《中国性科学》 2026年第2期35-43,共9页
目的采用文献计量学方法,分析2004年—2024年支持细胞在精子发生领域的研究热点和发展趋势。方法检索2004年—2024年Web of Science核心数据库、中国知网收录的支持细胞相关研究,共筛选出5679篇英文文献和455篇中文文献,采用CiteSpace... 目的采用文献计量学方法,分析2004年—2024年支持细胞在精子发生领域的研究热点和发展趋势。方法检索2004年—2024年Web of Science核心数据库、中国知网收录的支持细胞相关研究,共筛选出5679篇英文文献和455篇中文文献,采用CiteSpace软件对发文量、研究机构、作者合作网络及关键词进行系统性分析。结果英文关于支持细胞的研究发文量显著多于中文,且英文研究机构如Population Council在国际合作网络中处于核心地位,而中文研究机构的国际合作相对较少。英文作者在研究持续性、团队协作及发文量方面较有优势,而中文作者的研究多为短期或独立完成。关键词分析表明,英文研究主要聚焦于支持细胞的分子机制如基因表达、血睾屏障、精原干细胞等,而中文研究则更多关注传统动物模型及新兴领域如中药研究、铁死亡、信号通路等。结论基于文献计量分析结果,当前支持细胞在精子发生领域的研究中,英文文献在发文规模、合作网络、研究连续性及国际影响力上均显著占优,其研究已深入分子机制并整合多种前沿技术;中文研究则侧重于传统动物模型,并聚焦于中药干预与铁死亡等新兴方向。未来,中文研究需加强国际合作、稳定团队建设、系统阐释精子发生调控网络,并推动中药多靶点作用机制与现代生殖生物学的深度融合,以提升整体研究水平。 展开更多
关键词 支持细胞 精子发生 文献计量学 研究热点
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Effect of sodium arsenite on spermatogenesis, plasma gonadotrophins and testosterone in rats 被引量:25
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作者 Mahitosh Sarkar Gargi Ray Chaudhuri +1 位作者 Aloke Chattopadhyay Narendra Mohan Biswas 《Asian Journal of Andrology》 SCIE CAS CSCD 2003年第1期27-31,共5页
To investigate the effect of arsenic on spermatogenesis. Methods: Mature (4 months old) Wistar rats were intraperitoneally administered sodium arsenite at doses of 4, 5 or 6 mg-kg^-day1 for 26 days. Different varietie... To investigate the effect of arsenic on spermatogenesis. Methods: Mature (4 months old) Wistar rats were intraperitoneally administered sodium arsenite at doses of 4, 5 or 6 mg-kg^-day1 for 26 days. Different varieties of germ cells at stage VII seminiferous epithelium cycle, namely, type A spermatogonia (ASg), preleptotene spermatocytes (pLSc), midpachytene spermatocytes (mPSc) and step 7 spermatids (7Sd) were quantitatively evaluated, along with radioimmunoassay of plasma follicle-stimulating hormone (FSH), lutuneizing hormone (LH), testosterone and assessment of the epididymal sperm count. Results: In the 5 and 6 mg/kg groups, there were significant dose-dependent decreases in the accessory sex organ weights, epididymal sperm count and plasma concentrations of LH, FSH and testosterone with massive degeneration of all the germ cells at stage VII. The changes were insignificant in the 4 mg/kg group. Conclusion: Arsenite has a suppressive influence on spermatogenesis and gonadotrophin and testosterone release in rats. 展开更多
关键词 ARSENITE spermatogenesis GONADOTROPHINS TESTOSTERONE TESTIS
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Regulation of spermatogenesis by paracrine/autocrine testicular factors 被引量:22
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作者 Mahmoud Huleihel Eitan Lunenfeld 《Asian Journal of Andrology》 SCIE CAS CSCD 2004年第3期259-268,共10页
Spermatogenesis is a complex process regulated by endocrine and testicular paracrine/autocrine factors. Gonadotropins are involved in the regulation of several testicular paracrine factors, mainly of the IL-1 family a... Spermatogenesis is a complex process regulated by endocrine and testicular paracrine/autocrine factors. Gonadotropins are involved in the regulation of several testicular paracrine factors, mainly of the IL-1 family and testicular hormones. Testicular cytokines and growth factors (such as IL-1, IL-6, TNF, IFN-γ, LIF and SCF) were shown to affect both the germ cell proliferation and the Leydig and Sertoli cells functions and secretion. Cytokines and growth factors are produced by immune cells and in the interstitial and seminiferous tubular compartments by various testicular cells, including Sertoli, Leydig, peritubular cells, spermatogonia, differentiated spermatogonia and even spermatozoa. Corresponding cytokine and growth factor receptors were demonstrated on some of the testicular cells. These cytokines also control the secretion of the gonadotropins and testosterone in the testis. Under pathological conditions the levels of pro-inflammatory cytokines are increased and negatively affected spermatogenesis. Thus, the expression levels and the mechanisms involved in the regulation of testicular paracrine/autocrine factors should be considered in future therapeutic strategies for male infertility. 展开更多
关键词 spermatogenesis PARACRINE AUTOCRINE CYTOKINE growth factor
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Expression and localization of CKLFSF2 in human spermatogenesis 被引量:17
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作者 Gang Liu Zhong-Cheng Xin +5 位作者 Liang Chen Long Tian Yi-Ming Yuan Wei-Dong Song Xue-Jun Jiang Ying-Lu Guo 《Asian Journal of Andrology》 SCIE CAS CSCD 2007年第2期189-198,共10页
Aim: To investigate the expression and subcellular localization of chemokine-like factor superfamily 2 (CKLFSF2) in human testis and its potential role in spermatogenesis. Methods: A specific polyclonal antibody a... Aim: To investigate the expression and subcellular localization of chemokine-like factor superfamily 2 (CKLFSF2) in human testis and its potential role in spermatogenesis. Methods: A specific polyclonal antibody against CKLFSF2 was raised. The expression and cellular localization of CKLFSF2 in the seminiferous tubules was checked by immunohistochemistry method. Also, in situ hybridization was applied to localize the mRNA distribution. The EGFP- CKLFSF2 fusion protein was expressed in COS-7 cells to localize its subcellular location in vitro. In addition, the abnormal expression of CKLFSF2 in testes of patients with male infertility was assayed by reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemistry methods. Results: Having a close correlation with spermatogenesis defects, CKLFSF2 was specifically expressed in meiotic and post-meiotic germ cells, which were localized to the endoplasmic reticulum (ER) near the Golgi apparatus. Conclusion: CKLFSF2 could play important roles in the process of meiosis and spermiogenesis, and might be involved in the vesicular transport or membrane apposition events in the endoplasmic reticulum. 展开更多
关键词 spermatogenesis TESTIS chemokine-like factor superfamily INFERTILITY endoplasmic reticulum
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The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis 被引量:19
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作者 Guo-Lian Ding Ye Liu +4 位作者 Miao-E Liu Jie-Xue Pan Meng-Xi Guo Jian-Zhong Sheng He-Feng Huang 《Asian Journal of Andrology》 SCIE CAS CSCD 2015年第6期948-953,I0008-I0009,共8页
The effects of diabetes mellitus include long-term damages, dysfunctions, and failures of various organs. An important complication of diabetes is the disturbance in the male reproductive system. Glucose metabolism is... The effects of diabetes mellitus include long-term damages, dysfunctions, and failures of various organs. An important complication of diabetes is the disturbance in the male reproductive system. Glucose metabolism is an important event in spermatogenesis. Moreover, glucose metabolism is also important for maintaining basic cell activity, as well as specific functions, such as motility and fertilization ability in mature sperm. Diabetic disease and experimentally induced diabetes both demonstrated that either type 1 diabetes or type 2 diabetes could have detrimental effects on male fertility, especially on sperm quality, such as sperm motility, sperm DNA integrity, and ingredients of seminal plasma. Epigenetic modifications are essential during spermatogenesis. The epigenetic regulation represents chromatin modifications including DNA methylation, histone modifications, remodeling of nucleosomes and the higher-order chromatin reorganization and noncoding RNAs. If spermatogenesis is affected during the critical developmental window, embryonic gonadal development, and germline differentiation, environmentally-induced epigenetic modifications may become permanent in the germ line epigenome and have a potential impact on subsequent generations through epigenetic transgenerational inheritance. Diabetes may influence the epigenetic modification during sperm spermatogenesis and that these epigenetic dysregulation may be inherited through the male germ line and passed onto more than one generation, which in turn may increase the risk of diabetes in offspring. 展开更多
关键词 DIABETES epigenetic regulation SPERM spermatogenesis
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Effect of Lepidium meyenii(maca)roots on spermatogenesis of male rats 被引量:22
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作者 Gustavo F.Gonzales Ana Ruiz +2 位作者 Carla Gonzales León Villegas Amanda Cordova 《Asian Journal of Andrology》 SCIE CAS CSCD 2001年第3期231-233,共3页
Aim:To determine the effect of oral administration of an aqueous extract from the roots of Lepidium meyenii(maca)on spermatogenesis in adult male rats.Methods;Male rats received an aqueous extract of the root(66.7 mg ... Aim:To determine the effect of oral administration of an aqueous extract from the roots of Lepidium meyenii(maca)on spermatogenesis in adult male rats.Methods;Male rats received an aqueous extract of the root(66.7 mg in onemL)twice a day for 14 consecutive days.Results:Treatment with Lepidium meyenii resulted in an increase in theweights of testis and epididymis but not the seminal vesicle weight.The length and frequency of stages IX-XIV seminif-erous tubules,where mitosis occurred,were increased and stages I-VI were reduced in rats treated with Lepidiummeyenii.Conclusion;The Lepidium meyenii root invigorates spermatogenesis in male rats by acting on its initialstages(IX-XIV). 展开更多
关键词 spermatogenesis Lepidium meyenii MACA TRANSILLUMINATION
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