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  • 1
    Electronic Resource
    Electronic Resource
    The Gap Junctional Protein Connexin(Cx)43 in Testicular Cancer: its Loss Marks Progession from Carcinoma In Situ to Invasive Germ Cell Tumour (2005)
    Berlin, Germany : Blackwell Verlag GmbH
    Anatomia, histologia, embryologia 34 (2005), S. 0 
    Details
    ISSN: 1439-0264
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Carcinoma-in-situ (CIS) of the testis is known to be the pre-invasive stage of most human germ cell tumours (seminoma and non-seminoma), but the mechanisms leading to an increased pubertal proliferation of CIS cells after a long latency and to progression of CIS to an invasive malignancy are still not known. Additionally, CIS and seminoma have also been reported in equine testis (Veeramachaneni and Sawyer, 1998). The gap junctional protein and tumour suppressor gene connexin(cx)43 represents the predominant cx in human, canine and rodent testis so far and it is expected to play a key role for the regulation of both proliferation and differentiation of germ cells (spermatogonia and spermatocytes), and its gene- and protein-expression pattern is typical for the pubertal terminal differentiation of somatic Sertoli cells. Using cDNA-microarray analysis, in-situ hybridization (ISH), RT-PCR from tissue homogenate and semi-quantitative RT-PCR from well defined microdissected tubules with normal spermatogenesis, CIS, intratubular seminoma (ISe) and from seminoma cells from invasive seminoma we found a downregulation of cx43 starting in intratubular CIS, leading to a complete loss in most invasive seminoma cells. This indicates that regulation of cx43 expression takes place at transcriptional level confirming and expanding earlier studies of protein expression (Brehm et al., 2002). This reduction of cx43-expression suggests that an early intratubular derangement in cx43-gene expression and disruption of inter-cellular communication between Sertoli cells and/or Sertoli cells and pre-invasive tumour cells via cx43-gap junctions may play a role in the proliferation of CIS cells and seminoma cells and in the progression phase of testicular seminoma development.References  Veeramachaneni, D. N., and H. R.Sawyer, 1998: Carcinoma in situ and seminoma in equine testis. APMIS 106, 183–185.Brehm R., A. Marks, R. Rey, S. Kliesch, M. Bergmann and K. Steger, 2002: Altered expression of connexins 26 and 43 in Sertoli cells in seminiferous tubules infiltrated with carcinoma-in-situ or seminoma. J. Pathol. 197, 647–653.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1439-0264.2005.00669_16.x
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  • 2
    Electronic Resource
    Electronic Resource
    The Expression of Connexins during Growth and Development of Skeletal Elements in the Dog (2005)
    Berlin, Germany : Blackwell Verlag GmbH
    Anatomia, histologia, embryologia 34 (2005), S. 0 
    Details
    ISSN: 1439-0264
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Efficient and well-regulated intercellular communication is essential to organize the activities of the different cell populations involved during growth and concomitant structural maturation of the skeleton. For direct cell-cell communication gap junctions composed of connexins (Cx) are present. So far 21 Cx types have been identified in mammals, which differ in molecular permeability as well as tissue expression pattern. To characterize the Cx distribution in the developing canine skeleton, samples from humerus, scapula and lumbar vertebrae of Beagle dogs aged 1.5, 3, 4.5 months and 1.5 years were fixed in Bouin's solution, decalcified with 25% EDTA and embedded in paraffin wax. Using immunohistochemistry and in situ hybridization, the expression of Cx 26, 30, 31, 32, 43, and 45 was studied in bone tissue plus associated epiphyseal and growth plate cartilage. Of all bone cells, osteoblasts showed the largest Cx expression repertoire: they were positive for Cx 26, 30, 32 and 43. After transformation into bone lining cells Cx43 expression was lost while in osteocytes only Cx 26 and 32 was detected. A wide variety of Cx reactions was also found in osteoclasts: Cx 26, 30, 32, and 43. In contrast, chondrocytes showed a much more restricted Cx expression pattern. Positive reactions were only seen in hypertrophic chondrocytes of epiphyseal cartilage (Cx 26, 31, 32) and in the proliferative (Cx32) and hypertrophic zone (Cx 26 and 32) of growth plate cartilage. Additionally, Cx31 was strongly expressed in the cellular layer of the periosteum covering areas of intensive bone modelling in the puppies. Age- and microlocation-dependent variations in expression and/or staining intensity were also observed in the other Cx types. These results demonstrated that canine bone cells are capable of synthesizing a wide variety of Cx types during skeletal development, thus propagating different cellular signals via gap junctions in a differentially regulated and requirement orientated manner.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1439-0264.2005.00669_106.x
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  • 3
    Electronic Resource
    Electronic Resource
    Specific Localization of the Gap Junctional Protein Connexin 32 in Equine Gastric Mucosa (2005)
    Berlin, Germany : Blackwell Verlag GmbH
    Anatomia, histologia, embryologia 34 (2005), S. 0 
    Details
    ISSN: 1439-0264
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Gap junctional inter-cellular communication (GJIC) is known to be important in the maintenance of tissue homeostasis. Evidence is accumulating that GJIC plays an important role in the gastric mucosal defence system and that the loss of GJIC is associated with gastric ulcer formation. The prevalence of gastric ulceration in foals and horses is high. However, there are no studies about the presence of gap junctions in gastric mucosa of horses. The purpose of this study was to investigate the distribution pattern of the gap junction protein 32 in normal gastric mucosa of horses. Immunocytochemical observations were made with light microscopy on cryosections of fresh frozen gastric mucosa from the fundic region, pyloric region, margo plicatus and pars nonglandularis. Immunohistochemical staining was performed by standard immunoperoxidase techniques using an anti-connexin 32 polyclonal antibody. In Situ Hybridization, Western Blot Analysis and RT-PCR were performed to confirm the presence of connexin 32. In normal horse gastric mucosa, connexin 32 was abundant in the surface epithelium and in a decreasing staining gradient extending down to the neck of the glands. Gastric surface mucous cells are formed in the neck of the glands and migrate along the foveola toward the mucosal surface. So, immature forms of surface mucous cells are found in the generative zone and in the deep part of the foveola, whereas well-matured ones cover the upper part of the foveola and the luminal surface of the mucosa. Therefore, these findings are in line with other studies, which described larger and more numerous gap junctions in mature surface mucous cells than in immature cells. These results show that gap junctions develop during the maturation of surface mucous cells and suggest that GJIC between gastric surface mucous cells plays an important role in the regulation of cell differentiation and in tissue homeostasis. Further studies are required to investigate the distribution pattern of connexin 32 in the gastric mucosa of horses with gastric ulcer.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1439-0264.2005.00669_33.x
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  • 4
    Electronic Resource
    Electronic Resource
    Prophylactic perioperative use of clindamycin and metronidazole in vaginal hysterectomy without pelvic floor repair (1988)
    Springer
    Archives of gynecology and obstetrics 244 (1988), S. 53-57 
    Details
    ISSN: 1432-0711
    Keywords: Antibiotic prophylaxis ; Vaginal hysterectomy ; Clindamycin ; Metronidazole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We studied the effect of perioperative clindamycin (3×600 mg in 100 ml 0.9% saline), metronidazole (3×500 mg in 100 ml 0.9% saline) and a placebo (3×100 ml of 0.9% saline) in 120 patients having a vaginal hysterectomy without colporrhaphy. The rate of postoperative urinary tract infections was significantly higher in the placebo group, but there was no significant difference between the three groups in the days of postoperative fever (a temperature above 37°C) or in the length of hospital stay. One patient on placebo had a vault infection and another had a fever of unknown origin.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00931403
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