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Long-term alterations in the permeability of the blood-testis barrier following a single intratesticular injection of dilute aqueous glycerol.

The mechanism whereby glycerol exerts its antispermatogenic action is not known. The objective of this study was to determine, with the use of [3H]inulin and [125I]albumin by in vivo and in vitro methods, whether glycerol exerts its effect by altering the permeability of the blood-testis barrier (BTB). Adult male rats received a single intratesticular injection of either glycerol (10% or 20%; treated) or saline (control), and 2, 4, 8, 26, and 56 weeks after treatment, either [3H]inulin or [125I]albumin was administered either by infusion or directly to the testicular tissues. Radioactivity was measured in testicular tissue, rete testis fluid, and seminiferous tubular fluid. Following in vivo administration, the uptake of [3H]inulin by seminiferous tubules, rete testis fluid, and seminiferous tubule fluid was significantly greater in the treated than in the control testes at all times after treatment. Radiolabeled inulin, injected into isolated testes or added to medium in which isolated tubules were incubated, accumulated at significantly higher levels in the seminiferous tubule compartment of treated than control tissues. Rete testis fluid from treated testes, collected by micropuncture following efferent duct ligation, contained about 5- to 13-fold more radioactivity than fluid from controls. Following infusion of 50 microCi of [125I]albumin into the jugular vein, the accumulated radioactivity was significantly greater in testicular and epididymal tissues and in the seminiferous tubule fluid from treated than from control animals. In all experiments the significant differences between treated and control were maintained during the period of 2-56 weeks following glycerol treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

Albumins↗

Changes in protein composition of the luminal fluids along the epididymis of the tammar, Macropus eugenii.

Micropuncture samples of luminal fluid were collected from the rete testis and along the epididymis. Quantitative analyses showed that the ductuli efferentes reabsorb about half the protein leaving the testis. Considerable protein is secreted by the caput epididymidis (initial segment) and there is a net loss of protein from the corpus and cauda epididymidis. Denatured, polyacrylamide gel electrophoresis showed that there are 5 proteins in rete testis fluid which are not present in blood (Mr of 14,700, 22,800, 24,100, 43,000 and 44,800). One of these proteins (Mr 14,700) is lost from plasma in the ductuli efferentes and 2 (Mr 43,200 and 44,800) are lost in the corpus epididymidis. Twelve proteins appear in the epididymal plasma and are not present in rete testis fluid or blood: 6 appear in the caput epididymidis (Mr 30,000, 31,000, 32,300, 17,400, 18,700 and 21,400), 3 in the corpus epididymidis (Mr 12,800, 39,800 and 90,600) and 3 in the cauda epididymidis (Mr 10,900, 56,300 and 63,000). A protein with the same molecular weight as a blood protein (149,500) accumulates in the corpus and cauda epididymidis. None of the samples of luminal fluid contained particulate matter other than spermatozoa, indicating that the tammar is a useful animal for micropuncture studies.

Animals↗

Malignant large cell calcifying Sertoli cell tumor of the testis.

A 45-year old man presented with a slow-growing, unilateral beige testicular mass, with a diameter of 4 cm. The testosterone, FSH, LH, estradiol and betahCG serum levels were within normal limits, and there were no associated hormonal syndromes. The patient was treated with inguinal orchidectomy. Microscopically, the tumor was composed of nests of cells with large eosinophilic, slightly granular cytoplasm. There was only a mild degree of atypia and no mitotic activity. The tumor extended into the rete testis. There were intratumoral calcifications, and in the vicinity of the tumor, there was intratubular growth. Although this case is histologically similar to the three previously reported cases of clinically benign large cell calcifying Sertoli cell tumor of the testis with rete testis involvement, the current patient developed right sided para-aortic lymph node metastases 18 months after the initial diagnosis.

Calcinosis↗

Effects of estrogens on the testis of transsexuals: a pathological and immunocytochemical study.

Testes from five male-to-female transsexuals removed during sex-reversal surgery after administration of estrogens were studied histologically and with immunoperoxidase procedures to locate estrogen receptors (ER) and related antigens. Atrophy of the seminiferous tubules was observed in all cases; its degree, and a marked decrease in Leydig cells, correlated with low plasma gonadotropin levels (rather than with the duration of treatment). In all cases, the rete testis appeared hyperplastic and the other components (efferent ductules, epididymus) well preserved. The efferent ductules proved to be the only structure where ER can be located by the ER-ICA procedure, whereas staining for the p 29 ER-associated antigen is strongly positive both here and in the rete testis. The immunocytochemical data, in parallel with the observed biological effects, indicate that the rete testis and the efferent ductules and, to a minor degree, the epididymus and Leydig cells are the main direct targets of estrogens in the human testis.

Adult↗

Cystic dysplasia of the testis: a very rare paediatric tumor of the testis.

OBJECTIVES: To describe a case of cystic dysplasia of the testis (CDT), an uncommon cause of scrotal swelling in the pediatric patient. Clinic, therapy, fertility, and radiographic and pathologic findings are discussed and the 30 previously reported cases are reviewed. METHODS: A 9-year-old boy presented with asymptomatic scrotal swelling. A scrotal ultrasound showed a multicystic scrotal mass in the rete testis and an ipsilateral renal agenesis. The growth in size of the mass forced the authors to perform an operative exploration. RESULTS: Intraoperative findings included a multicystic mass in the rete testis of the right testicle. Testicle-sparing total removal of the multicystic mass was performed and the pathologic examination revealed a benign, multilobulated configuration of the cysts in the region of the rete testis. These findings were similar to those found in previously reported cases of CDT. Ipsilateral renal agenesis is the most common associated anomaly. As a pathogenetic factor, mal-junction of the Wolffian duct in the 5th week of gestation is most creditable. CONCLUSIONS: CDT is a rare cause of pediatric scrotal mass. When feasible, a testicle-sparing approach should be considered and all patients should undergo evaluation for associated urologic anomalies.

Child↗

Luminal composition and maturation of spermatozoa in the genital ducts of the African elephant (Loxodonta africana).

The mean spermatocrit and sodium, potassium and protein concentrations of fluid collected from the rete testis of the elephant were similar to values described for the ram. Sperm maturation, as assessed by the location of the cytoplasmic droplet in the middle pice, occurred in the distal head and the isthmus of the epididymis (middle segment). Spermatocrit determinations indicated that 96% of the fluid leaving the testis was reabsorbed by the efferent ducts and proximal initial segment, and 53% of the remainder was reabsorbed in the more distal parts of the head of the epididymis (initial and proximal middle segments). Sodium was reabsorbed in the same concentration as luminal fluid and not in amounts equimolar with potassium. The potassium concentration increased from 12.1 mequiv./l in rete testis plasma to 64.8 mequiv./l in the proximal head of the epididymis. About two thirds of the protein in rete testis fluid (3.8 mg/ml) was reabsorbed by the efferent ducts and more was absorbed by the head of the epididymis.

Animals↗

Distribution and fine structure of the lymphatic system in the human testis.

The distribution of lymph vessels in the human testis was investigated using ink injection methods, and light and electron microscopy. Lymph capillaries occur in the septula testis but are absent in the intertubular tissue. They consist of endothelial cells provided with an incomplete basal lamina and anchoring filaments of the adjacent connective tissue. Frequently, the endothelial cells are separated by gaps measuring up to 2 micron. The lymph capillaries of the septula testis are connected to lymph vessels in the rete testis and tunica albuginea. These vessels have occasional smooth muscle cells and valves. At the posterior margin of the testis, the network of lymph vessels merges into collecting ducts, which together with vessels derived from the rete testis are drained by the lymphatic system in the spermatic cord.

Endothelium↗

Androgen binding proteins of testis, epididymis, and plasma in man and monkey.

Androgen-binding protein (ABP) has been found in the cytosol of testicular and epididymal homogenates of several sub-primate species. In those species which had the plasma androgen binding protein, testosterone-estradiol-binding globulin (TeBG), ABP and TeBG were found to be physically similar. We investigated the possibility that ABP might exist in monkey and man using the cytosol of testicular and epididymal homogenates and aspirates obtained by direct micropuncture of the rete testis. In polyacrylamide gel electrophoresis, pH 7.8, testicular and epididymal cytosols of monkey and man were found to contain several binding proteins of different size and net charge that bind dihydrotestosterone. These binding proteins were either indistinguishable from TeBG or could be related to TeBG as size and/or charge isomers. No ABP was detectable in up to 200 mul of monkey rete testis fluid obtained by direct micropuncture, though ABP is detectable in as little as 5 mul of rat rete testis fluid. The data suggest that the ABP's detected in the testicular and epididymal cytosols in monkey and man represent isomeric forms of plasma TeBG, and their presence in testicular cytosol most likely derives from blood contamination.

Androgens↗

Monoclonal antibody 43-9F as a sensitive immunohistochemical marker of carcinoma in situ of human testis.

Invasive germ cell cancer can be prevented if the neoplasia is diagnosed at the stage of carcinoma in situ (CIS). In routine histologic examination CIS may be overlooked, particularly in prepubertal individuals. The detection of this early malignancy may be greatly facilitated by use of immunohistochemical staining. The authors investigated the sensitivity of an immunohistochemical staining procedure with monoclonal antibody 43-9F in detection of CIS. Testicular specimens from 19 adult and two prepubertal individuals with CIS were tested. Positive staining reaction on the surface of malignant germ cells was encountered in all 21 specimens with CIS. The epithelial cells of the excretory ducts between testis and epididymis, including rete testis and canaliculi efferentes, reacted also positively with 43-9F. No staining was observed in nonmalignant testicular cells including Sertoli cells or Leydig cells in any of these samples or in testicular biopsy specimens from 27 adult and 11 prepubertal subjects without evidence of testicular neoplasia. Monoclonal antibody 43-9F was also found to react with cells of all four tested invasive testicular germ cell tumors. Thus, the monoclonal antibody 43-9F is a sensitive immunohistochemical marker of CIS germ cells and may also be of potential value in detection of invasive testicular cancer.

Adult↗

The entry of alpha-chlorohydrin into body fluids of male rats and its effect upon the incorporation of glycerol into lipids.

The rate of entry of alpha-chlorohydrin into rat rete testis fluid has been studied using the 14-C and 36-Cl-labelled compounds. The alpha-chlorohydrin crosses the blood-testis barrier and the concentration of radioactivity in rete testis fluid attained blood levels within 45 min. Within 3 hr of a single injection of [14-C] alpha-chlorohydrin, radioactivity was widely distributed in body fluids, and was present in the lipids of the brain, testis, epididymis and epididymal fat pads. No radioactivity was found in tissue lipids following the administration of [36-Cl] alpha-chlorohydrin, which suggests that dechlorination of this compound occurs before its incorporation. Neither a single high dose nor repeated low doses of alpha-chlorohydrin induced changes in the incorporation of [14-C] glycerol into lipids of the brain, testis, epididymis and epididymal fat pads.

Animals↗

The antiestrogen ICI 182,780 induces early effects on the adult male mouse reproductive tract and long-term decreased fertility without testicular atrophy.

BACKGROUND: Estrogen receptors (ER) have important physiological roles in both the female and male reproductive systems. Previous studies using the estrogen receptor-alpha knockout mouse (alphaERKO) or antiestrogen treatment in adult rodents have shown that ERalpha is essential for normal function of the male reproductive tract. In the present study, time-response effects of the antiestrogen ICI 182,780 were determined to better understand ERalpha function in the adult male. METHODS: Adult male mice, 30 days old, were injected subcutaneously with ICI 182,780 (5 mg) once per week for 17 weeks. Tissues were fixed by vascular perfusion to study the time responses from day 2 to 125 post treatment. RESULTS: No difference was seen in body weight due to treatment. Testis weight was decreased 18% on day 59 and 21.4% on day 125. Other significant treatment-related effects included the following: 1) dilation of rete testis and efferent ductule lumen; 2) decreased height of the rete testis and efferent ductule epithelium; 3) decreased height of the supranuclear epithelial cytoplasm in efferent ductules; 4) decreased height of the efferent ductule epithelial microvilli, particularly in the proximal ductules; 5) decrease in the PAS-positive granules and endocytotic vesicles in nonciliated epithelial cells of efferent ductules; 6) capping and vesiculation of narrow cells in the initial segment of the epididymis; 7) accumulation of PAS-positive granules in apical cells of the caput epididymis; 8) increase in lysosomal granules in clear cells of the corpus and cauda epididymis; 9) limited induction of atrophic seminiferous tubules and abnormal spermatogenesis; and 10) decreases in the concentration of cauda sperm, progressive sperm motility and decreased fertility. CONCLUSIONS: Antiestrogen treatment of the pubertal male mouse resulted in reproductive effects similar to those observed in the alphaERKO mouse as early as day 4; however, testis weight did not increase substantially and total atrophy was not observed with extended treatment.

Animals↗

Tridimensional reconstruction and histology of the intratesticular seminal pathway in the hamster.

The present work reports a tridimensional reconstruction of the intratesticular seminal pathway in the hamster as studied with light microscopy of serial sections of the proximal pole of the testis. It has three portions: a "terminal segment" of the seminiferous tubules; the tubuli recti with three parts; and the rete testis with two parts, intratesticular and extratesticular. Experiments using ductuli efferentes ligation show a marked dilation of the rete testis and tubuli recti without a corresponding dilation of the seminiferous tubules. This may be due to a valve-like action of the cells in the terminal segment of the tubules.

Animals↗

Sequence of sperm cell surface differentiation and its relationship to exogenous fluid proteins in the ram epididymis.

To study successive surface changes of maturing ram spermatozoa, we determined the 125I-labeling patterns of testicular spermatozoa and of spermatozoa from 10 consecutive regions of the epididymis. Overall, three phases of cell surface transformations are distinguishable: Phase I occurs in the caput epididymidis and it is characterized by a series of rapid surface changes. The most striking surface transformations occur during transport of spermatozoa from the testis into the proximal caput epididymidis. All major surface components in the zones 78 to 115 kd disappear or are lost from the surface of testicular spermatozoa. Concurrently, several low molecular weight components (17 to 65 kd) appear or become increasingly accessible to 125I. Phase II represents a period of relative quiescence which is confined to the corpus epididymidis. Phase III takes place in the cauda epididymidis where several existing (97, 65 and 41 kd) and new (24 kd) proteins become the predominant features of the sperm cell surface. Electrophoretic analyses of luminal fluid proteins from corresponding regions of the testis and epididymis also show that the most striking changes occur between the rete testis and the proximal caput epididymidis. No rete testis fluid (RTF) components are detectable in luminal fluid of the proximal caput epididymidis. In the epididymis, however, fluid proteins are more persistent than sperm surface components. Several major fluid components (i.e., 95, 76, 21.5, 19.5 and 16 kd) persist throughout the epididymis. Other fluid proteins are of a more transient nature as, for example, a 25 kd molecular weight component (regions E1 through E6) or the 180, 62, 37 and 32 kd components in regions E4 to E10, the 270, 115 and 105 kd proteins in regions E6 to E10 and the 360, 145, 125 and 62 kd molecular weight components in regions E7 to E10. No direct relationships could be established between intrinsic surface components and exogenous fluid proteins from corresponding regions of the testis and epididymis. These results demonstrate a much greater complexity of sequential surface transformation in maturing epididymal spermatozoa than was predictable from our earlier studies of testicular and ejaculated spermatozoa. Apparently, ram spermatozoa must undergo extensive surface renovations in the caput epididymidis before the surface protein pattern typical of mature spermatozoa slowly develops.

Animals↗

Sperm maturation, fluid transport, and secretion and absorption of protein in the epididymis of the echidna, Tachyglossus aculeatus.

Extratesticular sperm maturation in the echidna mainly occurs in the initial segment of the ductus epididymidis. The process involves the development of motility, migration and loss of the cytoplasmic droplet, a decrease in permeability to Congo red and the formation of sperm bundles. The spermatozoa are supported in the bundles by a matrix of electron-dense material; the bundles are very motile is undiluted samples of luminal fluids. Micropuncture studies of anaesthetized echidnas showed that the ductuli efferentes absorb 74% of the fluid and 46% of the soluble protein that enters them. The initial segment of the ductus epididymidis absorbs 83% of the fluid which enters it, and its secretions increase the concentration of protein in luminal fluid by 107%. Denatured, linear-gradient polyacrylamide gel electrophoresis of micropuncture samples showed that 1 protein (apparent M4 = 100 500) which is not present in blood plasma is present in rete testis fluid, and a glycoprotein which is present in rete testis fluid (apparent Mr = 78500) is absorbed by the ductuli efferentes. Six proteins which are not present in blood plasma are secreted into the initial segment of the ductus epididymidis; 5 are glycoproteins (apparent Mr = 48500, 39000, 32000, 20500 and 19000) and one (apparent Mr = 82500) is not. The most prominent electrophoresis bands corresponded to the glycoproteins with apparent molecular weights of 48500, 20500 and 19000.

Animals↗

Cystic dysplasia of the testis. Light and electron microscopic study of three cases.

The testes of two premature newborns and a 9-year-old boy with cystic dysplasia were studied by light and electron microscopy. The histologic pattern of the three cases was similar, differing principally in the extension of the characteristic lesion. This consisted of multiple, anastomosing, irregular cystic spaces of varying sizes and shapes, separated by incomplete connective-tissue septa. The cysts were predominantly located in the mediastinum testis, and spread irregularly, displacing the testicular parenchyma, which was consequently compressed under the tunica albuginea. Electron microscopic examination revealed two types of epithelial cells (flattened and tall cells) lining the cystic spaces. These cells were similar to those lining the normal adult rete testis. Since the rete testis originates from the gonadal blastema, and the efferent ductules from the mesonephric ducts, an embryologic defect in the connection between both structures might be responsible for this lesion.

Child↗

The epididymal region of the Japanese quail (Coturnix coturnix japonica).

The epididymal region of the Japanese quail was studied histologically. The organ consists of the extratesticular portion of the rete testis, the ductuli efferentes proximales and distales, the ducti conjugentes and ductus epididymidis. Distinct tubuli recti link the seminiferous tubules with the rete testis. The non-ciliated cells of the ductuli efferentes proximales and distales show, between them, certain internal structural differences which were highlighted. In 40% of the birds, the ductus deferens showed dark-grey pigments, regarded as melanin. The epididymal region was generally similar in structure to that of the domestic fowl, turkey and duck.

Anatomy, Comparative↗

Growth factor activity in luminal fluids from the male reproductive tract of the ram, rat, tammar wallaby (Macropus eugenii) and Japanese quail (Coturnix coturnix japonica).

Growth factor activity in luminal fluids from the male reproductive tract was assayed by measuring the stimulation of [3H]thymidine incorporation into BALB/c 3T3 fibroblasts. The potency of fluids from the rete testis of the rat, ram, tammar wallaby and Japanese quail was much the same. However, about 90% of the activity in fluid from the rete testis of the rat and tammar was lost during its passage through the epididymis.

Animals↗