ABSTRACT
BACKGROUND: Testis-expressed sequence 101 (TEX101) was found to be highly expressed in testis and involved in acrosome reaction in previous studies. Recently, the metastasis suppressor function of TEX101 in cancer was disclosed, but the comprehensive investigation of its expression has rarely been reported. In this study, the expression features of TEX101 in normal human organs and seminoma were systematically analyzed. RESULTS: Immunohistochemistry demonstrated intense staining of TEX101 in human testis tissues; however, its expression in 27 other types of normal human organs, including the ovary, was negligible. Higher expression of TEX101 was observed in the spermatocytes and spermatids of the testis, but relatively lower staining was detected in spermatogonia. Western blotting showed a single TEX101 band of 38 kDa in human testis, but it did not correspond to the predicted molecular weight of its mature form at 21 KDa. Furthermore, we examined seminoma tissues by immunohistochemistry and found that none of the 36 samples expressed TEX101. CONCLUSIONS: Our data confirmed TEX101 to be a testis protein that could be related to the maturation process of male germ cells. The lack of TEX101 in seminoma indicated its potential role in tumor progression. This characteristic expression of TEX101 could provide a valuable reference for understanding its biological functions.
Subject(s)
Humans , Male , Female , Seminiferous Epithelium/metabolism , Testicular Neoplasms/metabolism , Seminoma/metabolism , Membrane Proteins/metabolism , Organ Specificity/physiology , Ovary/metabolism , Seminiferous Epithelium/pathology , Sperm Maturation/physiology , Spermatozoa/growth & development , Testicular Neoplasms/pathology , Testis/metabolism , Testis/pathology , Immunohistochemistry , Cell Differentiation , Blotting, Western , Seminoma/pathology , Gastrointestinal Tract/metabolism , Epithelium/metabolism , Lymphoid Tissue/metabolism , Nerve Tissue/metabolismABSTRACT
Programmed cell death in the form of apoptosis involves a network of metabolic events and may be triggered by a variety of stimuli in distinct cells. The nervous system contains several neuron and glial cell types, and developmental events are strongly dependent on selective cell interactions. Retinal explants have been used as a model to investigate apoptosis in nervous tissue. This preparation maintains the structural complexity and cell interactions similar to the retina in situ, and contains cells in all stages of development. We review the finding of nuclear exclusion of several transcription factors during apoptosis in retinal cells. The data reviewed in this paper suggest a link between apoptosis and a failure in the nucleo-cytoplasmic partition of transcription factors. It is argued that the nuclear exclusion of transcription factors may be an integral component of apoptosis both in the nervous system and in other types of cells and tissues
Subject(s)
Animals , Rats , Apoptosis , Nerve Tissue/growth & development , Retina/growth & development , Transcription Factors/metabolism , Animals, Newborn , Cell Differentiation , Nerve Tissue/cytology , Nerve Tissue/metabolism , Nuclear Envelope/metabolism , Retina/cytology , Retina/metabolismSubject(s)
Biochemical Reactions , Biochemistry/classification , Biochemistry/history , Biochemistry/methods , Nucleic Acids/metabolism , Amino Acids/metabolism , Blood Chemical Analysis/classification , DNA/metabolism , Energy Metabolism , Lipids/metabolism , Mitochondria/drug effects , Nerve Tissue/metabolism , Proteins/metabolism , RNA/metabolismABSTRACT
Intracellular localization of antileprosy drugs dapsone (DDS) and rifampicin (RFP) was carried out on skin and nerve lesions obtained from multidrug treated, multi (BL-LL)- and pauci (BT-TT) bacillary cases of leprosy using immunocytochemical techniques. Intracellular localization of the above drugs especially in macrophages and Schwann cells was aimed by using rabbit raised anti DDS and RFP polyclonal antibody in an indirect peroxidase assay. Our study records both intra and extracellular staining with anti DDS and RFP antibodies in the skin as well as nerve lesions of MB and PB cases treated with MDT. All the nerves under investigation had moderate to severe pathology and hence free diffusion of the drug could be attributed to the broken barrier. Basal lamina around the Schwann cell did not seem to form a barrier. It was also noted that the drug (metabolite) persisted over a long period of time).
Subject(s)
Animals , Dapsone/analysis , Humans , Immunoenzyme Techniques , Leprostatic Agents/analysis , Leprosy/drug therapy , Macrophages/metabolism , Mice , Nerve Tissue/metabolism , Rabbits , Rifampin/analysis , Schwann Cells/metabolism , Skin/metabolismABSTRACT
Experimental diabetes was induced in twenty rats using alloxan monohydrate. Another group of [10] normal rats of the same age and weight were served as control. Horse radish peroxidase [HRP] was injected I. V to demonstrate vascular permeability changes in sciatic nerves of these rats. Electron microscopic examination of ultrathin sections of sciatic nerves revealed that HRP reaction product was seen between the perineurial cells and within pinocytic vesicles of these cells in sciatic nerves of diabetic rats indicating failure of normal blood-nerve diffusion barrier. HRP reaction product was observed in the epineurium and did not penetrate into the endoneurium in sections of sciatic nerves of normal rats indicating normal blood-nerve diffusion barrier. It can be concluded that an increase in vascular permeability does occur in diabetic rats, resulting in impairment of blood-nerve diffusion barrier. The possible pathogenesis will be discussed