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[Untitled]
- Source :
- Histochemical Journal. 31:133-144
- Publication Year :
- 1999
- Publisher :
- Springer Science and Business Media LLC, 1999.
-
Abstract
- To examine the localization of von Hippel–Lindau (VHL) protein in human tissues, we produced four novel monoclonal antibodies against human VHL protein. Western blot analysis revealed that two of these antibodies recognized the epitope in amino acid sequence 60–89 of the VHL protein and the others recognized sequences 54–60 and 189–213. In a wild-type VHL gene-transfected cell line, immunocytochemistry and immunoelectron microscopy demonstrated the intracytoplasmic localization of VHL protein, particularly in mitotic cells. In normal human tissues, VHL protein was detected immunohistochemically in epithelial cells covering the body surface and the alimentary, respiratory, and genitourinary tracts; in secretory epithelial cells of exocrine and endocrine organs; in parenchymal cells of visceral organs; in cardiomyocytes; in neurons in nervous tissue; in lymphocytes in lymphoid tissue; and in macrophages. In pathological specimens, VHL protein was expressed in VHL-related tumor, as well as in endothelial cells, fibroblasts, and pericytes, all of which are involved in active angiogenesis. These findings suggest that these monoclonal antibodies can be useful for various immunological assays and that the VHL protein plays fundamental roles in physiological and pathological situations, especially in neovascularization.
- Subjects :
- Pathology
medicine.medical_specialty
endocrine system diseases
biology
medicine.diagnostic_test
medicine.drug_class
Angiogenesis
Immunoelectron microscopy
Immunocytochemistry
Cell Biology
urologic and male genital diseases
Monoclonal antibody
female genital diseases and pregnancy complications
Epitope
Western blot
Cell culture
medicine
biology.protein
Anatomy
Antibody
neoplasms
Subjects
Details
- ISSN :
- 00182214
- Volume :
- 31
- Database :
- OpenAIRE
- Journal :
- Histochemical Journal
- Accession number :
- edsair.doi...........d468a9606f7186d7d81ddae9ef346a6d
- Full Text :
- https://doi.org/10.1023/a:1003554712386