Navanukraw Pakpoom, Chotimanukul Sroisuda, Kemthong Taratorn, Choowongkomon Kiattawee, Chatdarong Kaywalee
Department of Obstetrics, Gynecology and Reproduction, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand.
National Primate Research Center of Thailand, Chulalongkorn University, Saraburi 18110, Thailand.
Animals (Basel). 2023 Jul 12;13(14):2282. doi: 10.3390/ani13142282.
FSHr antibodies have been shown to inhibit the differentiation of spermatogonia to primary spermatocytes, resulting in infertility without a pathological effect on reproductive organs. The aim of this study was to develop single-chain variable fragments (scFvs) against the follicular-stimulating hormone receptor (anti-FSHr) using phage-display technology and to evaluate the effects of intratesticular administration of the anti-FSHr scFv on testicular function and testosterone production. A phage clone against the extracellular domain of FSHr selected from a scFv phagemid library was analyzed for binding kinetics by surface plasmon resonance. Using ultrasound guidance, three adult macaques () were administered with 1 mL of 0.4 mg/mL anti-FSHr scFv (treatment) and 1 mL sterile phosphate buffer solution (control) into the left and right rete testis, respectively. Testicular appearance and volume, ejaculate quality, and serum testosterone levels were recorded on day 0 (before injection) and on days 7, 28, and 56 (after injection). Testicular tissue biopsies were performed on day 7 and day 56 to quantify the mRNA expressions of androgen binding protein (), inhibin subunit beta B (), and vascular endothelial growth factor A (). The results demonstrated that the anti-FSHr scFv molecule was calculated as 27 kDa with a dissociation constant (K) of 1.03 µM. The volume of the anti-FSHr scFv-injected testicle was reduced on days 28 and 56 compared with day 0 ( < 0.05). Total sperm number was reduced from day 0 (36.4 × 10 cells) to day 56 (1.6 × 10 cells) ( < 0.05). The percentage of sperm motility decreased from day 0 (81.7 ± 1.0%) to day 7 (23.3 ± 1.9%), day 28 (41.7 ± 53.4%), and day 56 (8.3 ± 1.9%) ( < 0.05). Sperm viability on day 0 was 86.8 ± 0.5%, which reduced to 64.2 ± 1.5%, 67.1 ± 2.2%, and 9.3 ± 1.1% on days 7, 28, and 56, respectively ( < 0.05). The expression of and on days 7 (14.2- and 3.2-fold) and 56 (5.6- and 5.5-fold) was less in the scFv-treated testicle compared with the controls ( < 0.05). On day 56, the expression of was less ( < 0.05) in the treated testis (1.3-fold) compared with the controls. Serum testosterone levels were unchanged throughout the study period ( > 0.05). This study characterized the anti-FSHr scFv and demonstrated that treatment with anti-FSHr ameliorates testicular function without altering testosterone levels, offering a potential alternative contraceptive for the long-tailed macaques.
促卵泡激素受体(FSHr)抗体已被证明可抑制精原细胞向初级精母细胞的分化,导致不育,但对生殖器官无病理影响。本研究的目的是利用噬菌体展示技术开发针对促卵泡激素受体的单链可变片段(scFvs)(抗FSHr),并评估睾丸内注射抗FSHr scFv对睾丸功能和睾酮产生的影响。通过表面等离子体共振分析从scFv噬菌粒文库中筛选出的针对FSHr细胞外结构域的噬菌体克隆的结合动力学。在超声引导下,分别向三只成年猕猴的左右睾丸网注射1 mL 0.4 mg/mL抗FSHr scFv(治疗组)和1 mL无菌磷酸盐缓冲溶液(对照组)。在第0天(注射前)以及第7、28和56天(注射后)记录睾丸外观和体积、射精质量以及血清睾酮水平。在第7天和第56天进行睾丸组织活检,以定量雄激素结合蛋白(ABP)、抑制素亚基βB(INHBB)和血管内皮生长因子A(VEGFA)的mRNA表达。结果表明,抗FSHr scFv分子计算分子量为27 kDa,解离常数(Kd)为1.03 μM。与第0天相比,在第28天和第56天,注射抗FSHr scFv的睾丸体积减小(P<0.05)。精子总数从第0天的(36.4×10⁶个细胞)减少到第56天的(1.6×10⁶个细胞)(P<0.05)。精子活力百分比从第0天的(81.7±1.0%)下降到第7天的(23.3±1.9%)、第28天的(41.7±5.34%)和第56天的(8.3±1.9%)(P<0.05)。第0天精子活力为86.8±0.5%,在第7、28和56天分别降至64.2±1.5%、67.1±2.2%和9.3±1.1%(P<0.05)。与对照组相比,在第7天(分别为14.2倍和3.2倍)和第56天(分别为5.6倍和5.5倍),scFv治疗组睾丸中ABP和INHBB的表达较低(P<0.05)。在第56天,与对照组相比,治疗组睾丸中VEGFA的表达较低(P<0.05)(1.3倍)。在整个研究期间,血清睾酮水平没有变化(P>0.05)。本研究对抗FSHr scFv进行了表征,并证明抗FSHr治疗可改善睾丸功能而不改变睾酮水平,为长尾猕猴提供了一种潜在的替代避孕方法。