Document Detail


Proprotein-processing endoprotease furin controls the growth and differentiation of gastric surface mucous cells.
MedLine Citation:
PMID:  9109428     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Gastric surface mucous cells originate from progenitor cells at the isthmus of the gastric gland, from where the cells migrate to the luminal surface. With migration they form secretory granules and express TGF alpha. We found that proprotein-processing endoprotease furin-positive cells were layered around the upper one fourth of the gastric glands of adult rats, whereas they were distributed along an outer epithelial layer in fetal rats. Because the furin-positive cell layer was localized from the upper cell proliferating zone to the less proliferating pit-cell region in the gastric gland unit, we examined the role of furin in the growth and differentiation of surface mucous cells by using the cell line, GSM06. This cell line is derived from the gastric surface mucous cells of transgenic mice harboring the temperature-sensitive simian virus 40 T antigen. At T antigen-active temperature (33 degrees C), the cells grew to confluency, whereas at T antigen-inactive temperature (39 degrees C), the cells ceased growing. At 33 degrees C, the cells exhibited a high level of furin expression with a negligible level of periodic acid Schiff (PAS)-positive materials and a low level of TGF alpha. In contrast, at 39 degrees C the cells produced a high level of PAS-positive materials, TGF alpha, and secretory granules, with a negligible level of furin expression. To further examine the role of furin, we established a GSM06 cell line introduced with either a sense or an antisense furin cDNA. The cells with sense furin expression produced fewer PAS-positive materials and a low level of TGF alpha even at 39 degrees C, whereas the cells with antisense furin expression exhibited more PAS-positive materials and TGF alpha even at 33 degrees C. When furin expression was suppressed by its antisense oligonucleotide, the cell growth was retarded with enhanced expression of the differentiated characteristics. Thus, we conclude that furin is instrumental in controlling the growth of the surface mucous cells.
Authors:
Y Konda; H Yokota; T Kayo; T Horiuchi; N Sugiyama; S Tanaka; K Takata; T Takeuchi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of clinical investigation     Volume:  99     ISSN:  0021-9738     ISO Abbreviation:  J. Clin. Invest.     Publication Date:  1997 Apr 
Date Detail:
Created Date:  1997-05-09     Completed Date:  1997-05-09     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  7802877     Medline TA:  J Clin Invest     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1842-51     Citation Subset:  AIM; IM    
Affiliation:
Department of Molecular Medicine, Gunma University, Showa-machi, Maebashi, Japan.
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MeSH Terms
Descriptor/Qualifier:
Animals
Antigens, Polyomavirus Transforming / genetics
Base Sequence
Cell Differentiation / physiology
Cell Division / physiology
Cell Line, Transformed
Culture Media, Conditioned
Female
Fetus / cytology,  enzymology
Furin
Gastric Mucosa / cytology*,  enzymology*,  physiology
Gene Expression / drug effects
Mice
Microscopy, Electron
Oligonucleotides, Antisense / genetics,  pharmacology
Pregnancy
Rats
Rats, Wistar
Stem Cells / cytology,  enzymology
Subtilisins / antagonists & inhibitors,  genetics,  physiology*
Transforming Growth Factor beta / metabolism
Chemical
Reg. No./Substance:
0/Antigens, Polyomavirus Transforming; 0/Culture Media, Conditioned; 0/Oligonucleotides, Antisense; 0/Transforming Growth Factor beta; EC 3.4.21.-/Subtilisins; EC 3.4.21.75/Furin
Comments/Corrections

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