Document Detail


Tumour lines from a spontaneous rat endometrial stromal sarcoma, showing dendritic cell-like and myofibroblastic cell-like phenotypes.
MedLine Citation:
PMID:  15144798     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A transplantable tumour (RY) and cell lines (RY-PB and clone RY-B-E3 isolated from RY-PB) were established from a naturally occurring endometrial stromal sarcoma (ESS) found in a 24-month-old female F344 rat. The primary tumour and RY tumours, which had been serially passaged in syngeneic female rats up to the 10th generation, consisted of spindle or round cells arranged in ill-defined bundles or sheets. Neoplastic cells of the primary and RY tumours, as well as cultured cells of RY-PB and RY-B-E3, showed positive reactions to vimentin, ED1/ED2 (both for rat macrophages/histiocytes), OX6 (for dendritic cells expressing rat MHC class II antigens), and lysosomal enzymes such as acid phosphatase and non-specific esterase, in varying degrees. Ultrastructurally, neoplastic cells characteristically had tubulovesicular system-like structures and variously developed lysosomes in the cytoplasm. Neoplastic cells also exhibited immunoexpression to an alpha-smooth muscle actin (alpha-SMA). The addition of transforming growth factor (TGF)-beta1 to RY-PB and RY-B-E3 cultures increased the number of alpha-SMA-positive cells, whilst the positive cell number was decreased by anti-TGF-beta antibody. The RT-PCR method revealed the expression of TGF-beta1 mRNA in the cultured cells. The present study showed that rat ESS-derived cells exhibited dendritic cell-like and myofibroblastic cell-like phenotypes. The histogenesis of ESSs in human beings and rats remains poorly understood, and these tumour lines may therefore become useful tools for further research.
Authors:
J Yamate; Y Yokoyama; D Kumagi; Y Tsukamoto; M Kuwamura; T Kotani; S Sakuma
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of comparative pathology     Volume:  131     ISSN:  0021-9975     ISO Abbreviation:  J. Comp. Pathol.     Publication Date:  2004 Jul 
Date Detail:
Created Date:  2004-05-17     Completed Date:  2004-12-15     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0102444     Medline TA:  J Comp Pathol     Country:  England    
Other Details:
Languages:  eng     Pagination:  38-51     Citation Subset:  IM    
Copyright Information:
Copyright 2004 Elsevier Ltd.
Affiliation:
Laboratories of Veterinary Pathology, Graduate School of Agriculture and Biological Sciences, Osaka Prefecture University, Gakuencho 1-1, Sakai, Osaka 599-8531, Japan.
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MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis / physiology
Cell Line, Tumor*
Cell Transplantation
DNA Fragmentation
Dendritic Cells / metabolism,  pathology
Endometrial Neoplasms / metabolism,  pathology*
Female
Fibroblasts / metabolism,  pathology
Immunohistochemistry
Microscopy, Electron, Transmission
Neoplasm Transplantation
RNA, Messenger / analysis
Rats
Rats, Inbred F344
Reverse Transcriptase Polymerase Chain Reaction
Sarcoma, Endometrial Stromal / metabolism,  pathology*
Sarcoma, Experimental / metabolism,  pathology*
Transforming Growth Factor beta / biosynthesis
Transforming Growth Factor beta1
Chemical
Reg. No./Substance:
0/RNA, Messenger; 0/TGFB1 protein, human; 0/Tgfb1 protein, rat; 0/Transforming Growth Factor beta; 0/Transforming Growth Factor beta1

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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