Siril Ariyaratne H B, Ian Mason J, Mendis-Handagama S M
Department of Animal Science, College of Veterinary Medicine, The University of Tennessee, Knoxville, Tennessee 37996, USA.
Biol Reprod. 2000 Sep;63(3):898-904. doi: 10.1095/biolreprod63.3.898.
Leydig cells in the adult rat testis differentiate during the neonatal-prepubertal period. However, the stimulus for the initiation of their differentiation is still not clear. In the present study our objectives were to test the effects of thyroid hormone and LH on the initiation of precursor cell differentiation into Leydig cells in the prepubertal rat testis. Four groups of Sprague-Dawley rats were used. All treatments began at postnatal Day 1. Rats in groups I, II, and III received daily s.c. injections of saline (200 microl, controls), triiodothyronine (T(3), 50 microg/kg body weight, hyperthyroid), and LH (ovine LH 10 microg/rat/day), respectively. Rats in group IV were made hypothyroid from postnatal Day 1 by adding 0.1% propylthiouracil (PTU) to their mother's drinking water. Testes of rats were collected at 7, 8, 9, 10, 11, 12, 16, and 21 days of age, fixed in Bouin's solution, and embedded in paraffin for immunocytochemical studies. Immunoexpression of 3beta-hydroxysteroid dehydrogenase (3beta-HSD) and LH receptors (LHR) in testicular interstitial cells (other than the fetal Leydig cells) was observed using the avidin-biotin method. In control rats, out of all spindle-shaped cell types in the testis interstitium, only the peritubular mesenchymal cells showed positive immunolabeling for 3beta-HSD, beginning from the postnatal Day 11. However, positive immunolabeling for LHR was first detected in these cells at Day 12, i.e., after acquiring the steroidogenic enzyme activity. In T(3)-treated rats 3beta-HSD positive spindle-shaped cells were first observed at Day 9 (i.e., 2 days earlier than controls), and LHR-positive cells were first observed on Day 11 (2 days later than obtaining 3beta-HSD immunoactivity); they were exclusively the peritubular mesenchymal cells. The 3beta-HSD- and LHR-positive spindle-shaped cells were absent in the testis interstitium of LH-injected rats from Days 7 through 12 but were present at postnatal Day 16. In addition, more fetal Leydig cell clusters and fetal Leydig cells in mitosis were present in LH-treated rats compared to rats in all other treatment groups. Following their first detection, the number of positive cells for each protein continued to increase at each subsequent age in controls, T(3)-, and LH-injected groups. In PTU rats, 3beta-HSD and LHR-positive spindle-shaped cells were absent throughout the experimental period. From these observations, it is possible to suggest the following regarding the developing rat testis interstitium. 1) The precursor cells for the adult generation of Leydig cells in the postnatal rat testis are the peritubular mesenchymal cells. 2) Luteinizing hormone does not initiate the onset of mesenchymal cell differentiation into Leydig cells, instead it delays this process. However, daily LH treatment causes mitosis in fetal Leydig cells and increase in fetal Leydig cell clusters. 3) Thyroid hormone is critical to initiate the onset of mesenchymal cell differentiation into adult Leydig cells.
成年大鼠睾丸中的莱迪希细胞在新生儿期至青春期前阶段发生分化。然而,其分化起始的刺激因素仍不清楚。在本研究中,我们的目的是测试甲状腺激素和促黄体生成素(LH)对青春期前大鼠睾丸中前体细胞分化为莱迪希细胞起始过程的影响。使用了四组斯普拉格-道利大鼠。所有处理均在出生后第1天开始。第I、II和III组大鼠分别每日皮下注射生理盐水(200微升,对照组)、三碘甲状腺原氨酸(T3,50微克/千克体重,甲状腺功能亢进组)和LH(羊LH 10微克/大鼠/天)。第IV组大鼠从出生后第1天起通过在其母鼠饮水中添加0.1%丙硫氧嘧啶(PTU)使其甲状腺功能减退。在出生后第7、8、9、10、11、12、16和21天收集大鼠睾丸,用布因氏液固定,石蜡包埋用于免疫细胞化学研究。采用抗生物素蛋白-生物素方法观察睾丸间质细胞(胎儿莱迪希细胞除外)中3β-羟基类固醇脱氢酶(3β-HSD)和LH受体(LHR)的免疫表达。在对照大鼠中,在睾丸间质的所有梭形细胞类型中,仅从出生后第11天起,睾丸周围间质细胞显示出3β-HSD阳性免疫标记。然而,在这些细胞中,LHR阳性免疫标记最早在第12天检测到,即在获得类固醇生成酶活性之后。在T3处理的大鼠中,最早在第9天观察到3β-HSD阳性梭形细胞(即比对照组早2天),最早在第11天观察到LHR阳性细胞(比获得3β-HSD免疫活性晚2天);它们均为睾丸周围间质细胞。从出生后第7天至12天,LH注射大鼠的睾丸间质中不存在3β-HSD和LHR阳性梭形细胞,但在出生后第16天存在。此外,与所有其他处理组的大鼠相比,LH处理的大鼠中存在更多有丝分裂期的胎儿莱迪希细胞簇和胎儿莱迪希细胞。在首次检测到之后,对照组、T3处理组和LH注射组中每种蛋白质的阳性细胞数量在随后的每个年龄阶段持续增加。在PTU大鼠中,在整个实验期间均不存在3β-HSD和LHR阳性梭形细胞。基于这些观察结果,对于发育中的大鼠睾丸间质可以提出以下几点。1)出生后大鼠睾丸中成年莱迪希细胞的前体细胞是睾丸周围间质细胞。2)促黄体生成素不会启动间质细胞分化为莱迪希细胞的起始过程,相反,它会延迟这一过程。然而,每日LH处理会导致胎儿莱迪希细胞有丝分裂并增加胎儿莱迪希细胞簇。3)甲状腺激素对于启动间质细胞分化为成年莱迪希细胞的起始过程至关重要。