Culture of mouse germ cells isolated from fetal gonads

Mouse germ cells isolated from male or female genital ridges at 121/2 days post coitum were cultured at room temperature for up to 6 days, with [3H]thymidine present in the culture medium for either the first 24 h or the last 24 h of each culture period. Germ cells were also isolated 131/2-161/2 days post coitum and cultured for 24 h in the presence of [3H]thymidine. The proportion of cells in metaphase, and the proportion of labelled interphase and metaphase nuclei, was recorded. The labelling index declined from 131/2 days onwards, after development either in vivo or in vitro. No labelled metaphase plates were seen after 24 h in the presence of [3H]thymidine, suggesting that under these culture conditions the duration of the G2 phase exceeded 24 h. The results showed that the culture system, in spite of the low temperature, allowed the germ cells to replicate their DNA and undergo mitosis for up to 6 days. Addition of db-cAMP to the culture medium proved highly toxic to male germ cells, and did not markedly increase the proliferation rate of female germ cells.     

Significance of germ cells for the expression of testicular endocrine function in rats

Germ-cell depletion was induced in rats by busulphan administration during the fetal period (Group B). Although a sigmoidal increase of serum testosterone concentration was observed 1 h after the administration of graded doses of hCG (0.3-15.0 i.u./100 g body weight) in intact rats and those in Group B, a shift in the dose-response curve to the right was observed in the latter, suggesting that the sensitivity of testicular response to gonadotrophin was lower in germ cell-depleted rats. However, since the sensitivity was almost identical for both groups of rats for isolated Leydig cells incubated in vitro for 3 h with hCG (0.5-312.5 i.u./ml), the intrinsic nature of the cells was not affected in Group B rats. When the responses of testicular tissue blocks were examined in the in-vitro incubation system, reduced sensitivity reappeared for those from Group B rats, and the presence of testicular tissue components including seminiferous tubules was considered to be responsible for the difference in Leydig cell sensitivity between intact rats and those exposed to busulphan. By the combination of in-vivo and in-vitro experiments, we have demonstrated that germ cells are involved in the endocrine function of the testis.     

Differentiation of female chicken primordial germ cells into spermatozoa in male gonads

In avian species, the developmental fate of different-sex germ cells in the gonads is unclear. The present study attempted to confirm whether genetically female germ cells can differentiate into spermatozoa in male gonads using male germline chimeric chickens produced by the transfer of primordial germ cells (PGC), and employing molecular biological methods. As a result of Southern hybridization, specific sequences of the W chromosome (the female specific sex chromosome in birds) were detected in the genomic DNA extracted from one out of four male germline chimeric chickens. When two-color in situ hybridization was conducted on the spermatozoa of this germline chimera, 0.33% (average) of the nuclei of each semen sample showed the fluorescent signal indicating the presence of the W chromosome. The present study shows that female PGC can differentiate into spermatozoa in male gonads in the chicken. However, the ratio of produced W chromosome-bearing (W-bearing) spermatozoa fell substantially below expectations. It is therefore concluded that most of the W-bearing PGC could not differentiate into spermatozoa because of restricted spermatogenesis.     

On the number of founding germ cells in humans

Background  

The number of founding germ cells (FGCs) in mammals is of fundamental significance to the fidelity of gene transmission between generations, but estimates from various methods vary widely. In this paper we obtain a new estimate for the value in humans by using a mathematical model of germ cell development that depends on available oocyte counts for adult women.     

Reaggregates of cells from rat testis resemble developing gonads

Reaggregates prepared from newborn rat testis cells in Moscona-type rotation cultures were analyzed and compared with normal fetal (12-21 days) and newborn testes at the light and electron microscope level. After 25 h of culture, the aggregates resembled normal testicular tissue. The cells of the surface layer were spindle-shaped and connected by adherent junctions. The epithelial cords were composed exclusively of Sertoli cells and were surrounded by elongated cells resembling the developing myoid cells in newborn testes. The basal aspect of the cords was covered by a layer of flocculent material which, in places, was organized like an ordinary basement membrane. Individual spermatogonia with pseudopodes were observed in the interstitial tissue. Some Leydig cells were organized into small clusters like those typical in newborn testes. The present observations indicate that, histologically, the reaggregation of separated testicular cells resembles the differentiation of embryonic male gonads.     

Development of the endocrine function of the adrenals and gonads of Papio hamadryas in postnatal ontogeny

The hormonal functions of suprarenal glands and gonads were studied in the sacred baboon males and females during different periods of postnatal development. This in view, the content of cortisol, 11-deoxycortisol, pregnenolone, progesterone, 17-oxypregnenolone, 17-oxyprogesterone, 20 alpha-dihydroprogesterone, estrone and estradiol was determined using the radioimmunoassay. The early activation of secretion of the suprarenal androgens, characteristic of the man, is absent during the sexual maturation of the sacred baboon males and females. The level of corticosteroids and their basic precursors, characteristic of the adult sacred baboons, is extablished by the end of 3rd year of life.     

Atypical flagellar structure associated with endocrine cells of rat pituitary

Atypical flagellar structures containing eight subfibers arrayed around a single, central element (8 + 1) are associated with pituitary secretory cells, largely gonadotropes. Less frequently, flagella with a 7 + 2 pattern are seen. Both types appear commonly in pituitary tissues obtained from both male and female rats above 1 year of age and appear to penetrate the cells. Except for the pattern of the array, the structures are similar in dimension to commonly observed flagellar structures (9 + 2) when viewed in sections cut either in perpendicular or sagittal to the major axis. The (8 + 1) flagella are observed both singly and in pairs. Steroidal milieu (ovariectomy with or without steroid replacement) does not seem to influence their appearance. Flagella with the common 9 + 2 arrangement are not observed in the rat pituitary.     

The role of brain noradrenaline in regulating the endocrine function of the gonads in male brown rats selected for behavior

In two groups of gray rats--nonaggressive ones, selected by the lack of aggression towards investigator, and aggressive animals--studies have been made on the relationship between noradrenaline system of the brain and the activity of pituitary-testicular system. In tame rats, less evident dependence of the gonadal activity on activating effect of noradrenaline was noted. After injection of norepinephrine, dopamine, and serotonin in the same brain region. *****were less significant in tame rats as compared to those in aggressive ones. The disturbed relationship between noradrenaline system of the brain and hypothalamo-pituitary-testicular complex is presumably one of the causes of associate changes in the reproductive system during selection for the domestic type of behaviour.     

The functional state of thymus cells following microwave exposure of endocrine glands

Following local microwave exposure (460 MHz, 120 mW/cm2) of rabbits using fluorescent probes and chemiluminescent analysis, conformational rearrangements in nuclear and cytoplasmic membranes and in thymus cell chromatin of the animals as well as changes in the intensity of the lipid free radical peroxidation were seen. The character of the changes observed depended both on the localization of the exposure and on the number of exposures.     

Chick gonad differentiation following excision of primordial germ cells

The differentiation of embryonic chick gonads lacking germ cells was compared to that of normal chick gonads to determine whether the somatic elements of sterile avian gonads will undergo normal sexual differentiation. Primordial germ cells were removed by surgical excision of anterior germinal crescent from early embryos, Hamburger and Hamilton stages 6–11. Surgically treated and control embryos were sacrificed at 6, 15, and 20 days of incubation, and their gonads were studied histologically. Analysis of differentiation was based on morphological criteria at the cellular, tissue, and organ levels. In both male and female embryos, the somatic elements of the gonads differentiated normally in the absence of germ cells. The significance of these results for understanding the controls of differentiation of both the somatic gonad and the germ cells in birds is discussed and correlated with similar results in mammals.     

Binding of fluorescent lectins to the surface of germ cells from fetal and early postnatal mouse gonads

Fluorescent lectins were used to study the chemical nature of carbohydrate moieties present on the surface of female and male germ cells isolated from mouse gonads during fetal and early posnatal development. Concanavalin A (ConA), lens culinaris agglutinin (LCA), ricinus communis agglutinin (RCA_I) and wheat germ agglutinin (WGA) bound intensely to the germ cell plasma membrane at all stages studied. Other lectins such as ulex europaeus agglutinin (UEA_I) and agglutinin (SBA) did not bind or bound moderately (SBA to female germ cells only). Distinct developmental-related changes were observed when female germ cells were labeled with fluorescein-conjugated peanut agglutinin (PNA) or dolichos biflorus agglutinin (DBA). DBA and PNA binding was absent or weak in fetal female and male germ cells, but became intensely positive in oocytes in the immediate postnatal period. The percentage of oocytes stained with DBA increased during the first three days after birth, and from day 3–4 onwards all oocytes were strongly labeled. I suggest that these changes in lectin binding reflect changes in biochemical structure of the oocyte surface related to differentiative events occurring in the mouse ovary immediately after birth.     

骨骼肌的内分泌功能

长期以来,骨骼肌被认为是一种效应器官,接受神经和体液的调节。近年大量实验研究资料发现骨骼肌也具有分泌活性物质的功能,能表达、合成和分泌多种生物信号分子,包括调节肽、细胞因子和生长因子等,也是一种重要的内分泌器官。骨骼肌分泌的活性物质以旁分泌和／或自分泌方式调节骨骼肌的生长、代谢和运动功能;甚至以血液循环内分泌的方式调节机体远隔器官组织的功能。骨骼肌生成和分泌的活性物质在运动系统疾病和某些全身性疾病的发病中具有重要的作用。本文将对骨骼肌分泌的主要活性物质及其生理和病理生理学意义进行综述。     

骨骼的内分泌功能

既往认为骨骼是支持机体基本结构和参与运动及钙磷代谢的主要器官。近年发现组成骨骼的成骨细胞和破骨细胞能合成和分泌多种骨调节蛋白、生长因子、脂肪因子、炎症因子和心血管活性肽等多种生物活性物质,以旁/自分泌方式调节骨骼系统功能,并能通过血液循环远距分泌的方式,调节机体能量代谢、炎症反应和内分泌稳态等。     

Chronic cyclophosphamide treatment alters the expression of stress response genes in rat male germ cells

Increases in the survival rate of men treated with chemotherapeutic drugs and their desire to have children precipitate concerns about the effects of these drugs on germ cells. Azoospermia, oligospermia, and infertility are common outcomes resulting from treatment with cyclophosphamide, an alkylating agent. Exposure of male rats to cyclophosphamide results in dose-dependent and time-specific adverse effects on progeny outcome. Elucidation of the effects of chronic low-dose cyclophosphamide treatment on the expression of stress response genes in male germ cells may provide insight into the mechanisms underlying such adverse effects. Male rats were gavaged with saline or cyclophosphamide (6 mg/kg) for 4-5 wk; pachytene spermatocytes, round spermatids, and elongating spermatids were isolated; RNA was extracted and probed on cDNA arrays containing 216 cDNAs. After saline treatment, 125 stress response genes were expressed in pachytene spermatocytes (57% of genes studied), 122 in round spermatids (56%), and 83 in elongating spermatids (38%). Cyclophosphamide treatment reduced the number of genes detected in all germ cell types. The predominant effect of chronic cyclophosphamide exposure was to decrease the expression level of genes in pachytene spermatocytes (34% of genes studied), round spermatids (29%), and elongating spermatids (4%). In elongating spermatids only, drug treatment increased the expression of 8% of the genes studied. The expression profiles of genes involved in DNA repair, posttranslational modification, and antioxidant defense in male germ cells were altered by chronic cyclophosphamide treatment. We hypothesize that the effects of cyclophosphamide exposure on germ cell gene expression during spermatogenesis may have adverse consequences on male fertility and progeny outcome.     

Differentiation of donor primordial germ cells into functional gametes in the gonads of mixed-sex germline chimaeric chickens produced by transfer of primordial germ cells isolated from embryonic blood

This study was carried out to elucidate whether primordial germ cells, obtained from embryonic blood and transferred into partially sterilized male and female recipient embryos, could differentiate into functional gametes and give rise to viable offspring. Manipulated embryos were cultured until hatching and the chicks were raised until maturity, when they were mated. When the sex of the donor primordial germ cells and the recipient embryo was the same, 15 out of 22 male chimaeric chickens (68.2%) and 10 out of 16 female chimaeric chickens (62.5%) produced donor-derived offspring. When the sex of the donor primordial germ cells and the recipient embryo was different, 4 out of 18 male chimaeric chickens (22.2%) and 2 out of 18 female chimaeric chickens (11.1%) produced donor-derived offspring. The rates of donor-derived offspring from the chimaeric chickens were 0.6-40.0% in male donor and male recipient and 0.4-34.9% in female donor and female recipient. However, the rates of donor-derived offspring from the chimaeric chickens were 0.4-0.9% in male donor and female recipient and 0.1-0.3% in female donor and male recipient. The presence of W chromosome-specific repeating sequences was detected in the sperm samples of male chimaeric chickens produced by transfer of female primordial germ cells. These results indicate that primordial germ cells isolated from embryonic blood can differentiate into functional gametes giving rise to viable offspring in the gonads of opposite-sex recipient embryos and chickens, although the efficiency was very low.     

Limitation on the number of germ cells in the fetal ovary of the rat by older ovaries, in vitro

Ovaries from 9-day-old rats co-cultured for 4 days in vitro with ovaries from 13.5-day-old fetal rats prevent the proliferation of the oogonia in the fetal ovaries (germinostatic effect) and produce the anti-Müllerian substance. The hypothesis that the germinostatic and anti-Müllerian activities are not due to the same factor is discussed.     

The clathrin interacting protein Clint/epsinR in rat testicular germ cells

The plasma membrane and the trans-Golgi network (TGN) are major intracellular sites for clathrin-mediated membrane budding. Only recently has the clathrin interacting protein Clint/epsinR/enthoprotin been identified, which is thought to be involved in clathrin-dependent membrane budding from the TGN. Using immunocytochemistry, we now report the presence of Clint in the Golgi region of spermatocytes and spermatids of the rat testis. Together with subcellular fractionation experiments, our data show that, in male germ cells, Clint behaves as a peripheral membrane protein that is probably involved in TGN-related vesicle budding. Moreover, the immunostaining of the acrosome in round and elongating spermatids indicates that Clint operates in membrane traffic between the TGN and the acrosome. It may thus be speculated that the protein is involved in the biogenesis and shaping of acrosomal membranes.