Research Group for Comparative Endocrinology, Department of Experimental Zoology, University of Utrecht, Padualaan 8, 3584 CH, Utrecht, The Netherlands.
Fish Physiol Biochem. 1993 Jul;11(1-6):255-63. doi: 10.1007/BF00004573.
In an ultrastructural immunocytochemical study we investigated the development of the gonadotropic cells in the pituitary of two to six months old male African catfish in relation to testicular development. In this period, pituitary and testicular tissue samples were collected on five occasions (groups I-V). Blood samples could only be taken from the fish in groups III-V. The testicular development was divided in three stages i.e., immature (only spermatogonia, group I), early (spermatogonia and spermatocytes, groups II and III) and advanced (all germ cell stages including spermatozoa, groups IV and V) spermatogenesis. 11-Ketotestosterone blood levels were low, except for the last group. Antisera were raised against the complete catfish α,βGTH-II, as well as to the separate α- and β-subunits of catfish GTH-II. In the proximal pars distalis of immature fish, undifferentiated cells, somatotrops, putative thyrotrops (pTSH) and putative gonadotrops (pGTH) were found. In the two latter, secretory granules were labeled with anti-αGTH, but not with anti-βGTH-II. pTSH- and pGTH-cells were distinguished on the basis of the size of their secretory granules. During early spermatogenesis, two classes of putative gonadotrops could be distinguished. One type had the same immunocytochemical and ultrastructural characteristics as in immature fish; the secretory granules in the second cell type, which was more abundant, were also immunopositive for anti-βGTH-II. The mean volume of the secretory granules in these GTH-II cells was three times larger than that in the early appearing pGTH-cells. In addition, the later appearing GTH-II cells contained large inclusions, known as globules. These structures labeled with anti-αβGTH-II and with anti-βGTH-II, but not with anti-αGTH. It is assumed that the globules are involved in a differential storage and/or breakdown of the GTH-II subunits. During advanced spermatogenesis the two gonadotropic cell types could still be distinguished, but the early appearing pGTH-cell type was scarce. The present observations permit the conclusion that the early appearing cells may be GTH-I cells. However, definitive proof about their identity depends on the availability of antibodies or cDNA probes specific for GTH-I.
在一项超微结构免疫细胞化学研究中,我们研究了 2 至 6 月龄雄性非洲鲶鱼垂体中与睾丸发育相关的促性腺细胞的发育。在此期间,在五次(I-V 组)采集了垂体和睾丸组织样本。仅在 III-V 组的鱼中可以采血。睾丸发育分为三个阶段,即不成熟(仅精原细胞,I 组),早期(精原细胞和精母细胞,II 组和 III 组)和晚期(包括精子在内的所有生殖细胞阶段,IV 组和 V 组)精子发生。11-酮睾酮的血液水平较低,除了最后一组。针对完整的鲶鱼α、βGTH-II 以及鲶鱼 GTH-II 的单独α-和β-亚单位产生了抗血清。在未成熟鱼的近侧脑垂体中,发现了未分化细胞、生长激素细胞、假定促甲状腺激素(pTSH)和假定促性腺激素(pGTH)。在后两种中,分泌颗粒用抗αGTH 标记,但不与抗βGTH-II 标记。pTSH 和 pGTH 细胞基于其分泌颗粒的大小来区分。在早期精子发生期间,可以区分两类假定的促性腺激素。一种类型具有与未成熟鱼相同的免疫细胞化学和超微结构特征;第二种细胞类型的分泌颗粒也对抗βGTH-II 呈免疫阳性,该细胞类型更为丰富。这些 GTH-II 细胞的分泌颗粒的平均体积是早期出现的 pGTH 细胞的三倍。此外,后来出现的 GTH-II 细胞含有大的包含体,称为小球体。这些结构用抗αβGTH-II 和抗βGTH-II 标记,但不与抗αGTH 标记。据假设,小球体参与 GTH-II 亚基的差异储存和/或分解。在晚期精子发生期间,仍然可以区分两种促性腺激素细胞类型,但早期出现的 pGTH 细胞类型很少。目前的观察结果表明,早期出现的细胞可能是 GTH-I 细胞。然而,关于它们的身份的明确证据取决于是否可以获得针对 GTH-I 的特异性抗体或 cDNA 探针。