Oatley J M, Tibary A, de Avila D M, Wheaton J E, McLean D J, Reeves J J
Department of Animal Sciences, Center for Reproductive Biology, Washington State University, Pullman 99164, USA.
J Anim Sci. 2005 Mar;83(3):604-12. doi: 10.2527/2005.833604x.
Spermatogonial stem cell transplantation is a technique that has potential in livestock to enhance genetic gain and generate transgenic offspring through the male germ line. A means for depletion of endogenous germ cells in a recipient's seminiferous tubules is necessary for this technology to be applied. The objectives of this study were to evaluate several methods for depletion of endogenous germ cells in the testes of adult rams and to evaluate ultrasound-guided injections into the rete testes as a means for infusing a suspension into the seminiferous tubules. Sixteen adult rams were randomly divided into 4 treatment groups (n = 4 per group). Treatments consisted of active immunization against LHRH (IMM), localized testicular irradiation (IR), LHRH immunization + irradiation (IMM+IR), and untreated control. Serial bleedings were conducted pretreatment and monthly after treatment for 4 mo, at which time all rams were castrated. Both IMM and IMM+IR rams received exogenous gonadotropin in the form of Perganol weekly for 8 wk before castration to bypass the immunization. All rams also received an ultrasound-guided injection of PBS containing 0.4% trypan blue into the rete testis of one testicle before castration. Rams receiving IMM and IMM+IR treatments had higher (P < 0.05) average percentages of seminiferous tubule cross sections with depleted germ cells compared with controls. Serum testosterone was decreased (P < 0.05) in IMM and IMM+IR rams 1 mo after treatment and throughout the remainder of the study compared with controls and IR rams, which were not different from each other. Serum inhibin concentration was unchanged in all rams following treatment indicating that Sertoli cell function was unaltered. A greater (P < 0.05) average percentage of the total testicular area could be filled with the trypan blue solution by rete testis injection in IMM and IMM+IR rams. These data demonstrate the depletion of endogenous germ cells in adult ram testes without alteration of Sertoli cell viability and function that have potential as methods for preparing recipient animals for germ cell transplantation.
精原干细胞移植是一项在牲畜领域具有潜力的技术,可通过雄性生殖系提高遗传增益并产生转基因后代。对于该技术的应用而言,一种耗尽受体生精小管内源性生殖细胞的方法是必要的。本研究的目的是评估几种耗尽成年公羊睾丸内源性生殖细胞的方法,并评估超声引导下向睾丸网注射作为向生精小管注入悬浮液的一种手段。16只成年公羊被随机分为4个治疗组(每组n = 4)。治疗方法包括针对促黄体生成素释放激素(LHRH)的主动免疫(IMM)、局部睾丸照射(IR)、LHRH免疫 + 照射(IMM+IR)以及未治疗的对照组。在治疗前及治疗后每月进行连续采血,持续4个月,此时所有公羊均被阉割。IMM和IMM+IR组的公羊在阉割前每周接受8周的以倍他米松形式的外源性促性腺激素,以绕过免疫反应。所有公羊在阉割前还接受了超声引导下向一侧睾丸的睾丸网注射含0.4%台盼蓝的磷酸盐缓冲盐水(PBS)。与对照组相比,接受IMM和IMM+IR治疗的公羊生精小管横切面中生殖细胞耗尽的平均百分比更高(P < 0.05)。与对照组和IR组公羊相比,IMM和IMM+IR组公羊在治疗后1个月及研究的其余时间血清睾酮水平降低(P < 0.05),而对照组和IR组之间无差异。治疗后所有公羊的血清抑制素浓度均未改变,表明支持细胞功能未受影响。通过向睾丸网注射,IMM和IMM+IR组公羊的睾丸总面积中被台盼蓝溶液填充的平均百分比更高(P < 0.05)。这些数据表明,成年公羊睾丸内源性生殖细胞被耗尽,而支持细胞的活力和功能未改变,这些方法有可能作为为生殖细胞移植准备受体动物的方法。