C18. Role of nitric oxide in deregulation of oral epithelial cell proliferation after ionizing radiation

Nitric Oxide ◽  
2007 ◽  
Vol 17 ◽  
pp. 24
Author(s):  
M. Kang ◽  
R. Kim ◽  
R.H. Kim ◽  
K.H. Shin ◽  
N.H. Park
Keyword(s):  
Nitric Oxide ◽  
Cell Proliferation ◽  
Epithelial Cell ◽  
Ionizing Radiation ◽  
Epithelial Cell Proliferation ◽  
Oral Epithelial Cell ◽  
Oral Epithelial

Ontogeny of cell proliferation and DNA synthesis in rat colon: role of glucocorticoids

1983 ◽  
Vol 244 (5) ◽  
pp. G469-G474 ◽  
Author(s):  
J. P. Buts ◽  
R. De Meyer ◽  
J. Kolanowski
Keyword(s):  
Cell Proliferation ◽  
Epithelial Cell ◽  
Dna Synthesis ◽  
Mitotic Index ◽  
Dna Content ◽  
Thymidine Incorporation ◽  
Rat Colon ◽  
Epithelial Cell Proliferation ◽  
New Findings

This study was undertaken to determine whether the rat colon exhibits ontogenic changes in epithelial cell proliferation and DNA synthesis during growth. DNA synthesis was measured at intervals after birth in four colonic segments by the incorporation rates of [3H]thymidine. The labeled crypt cell index was determined by radioautography. New findings from our study are that 1) in each colonic segment of suckling rats, [3H]thymidine incorporation rate overshot the adult levels (49-119%) with a peak occurring at day 14 postpartum, 2) between days 14 and 20, the incorporation rates declined sharply to adult values and remained thereafter unchanged until adulthood; during the same period, the labeled and mitotic index decreased, respectively, from 52 to 19% and from 3.58 to 1.43%, 3) the decrease in DNA synthesis and in cell proliferation rates was concomitant with an upsurge in plasma total corticosterone initiated on day 14, and 4) treatment of 10-day-old sucklings with physiological doses of hydrocortisone for 4 consecutive days significantly depressed (P less than 0.01) colonic DNA content and DNA synthesis rates to levels about 45-67% of the control values. These data indicate that growth of the colon may be under the control of glucocorticoid secretion at the weaning period.

scholarly journals The role of nickel accumulation and epithelial cell proliferation in orthodontic treatment-induced gingival overgrowth

2007 ◽  
Vol 29 (6) ◽  
pp. 555-558 ◽  
Author(s):  
U. K. Gursoy ◽  
O. Sokucu ◽  
V.-J. Uitto ◽  
A. Aydin ◽  
S. Demirer ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Epithelial Cell ◽  
Orthodontic Treatment ◽  
Epithelial Cell Proliferation ◽  
Gingival Overgrowth ◽  
Nickel Accumulation

scholarly journals Role of zonula occludens in reduced epithelial cell proliferation by hypertonic stress

2013 ◽  
Vol 27 (S1) ◽  
Author(s):  
Xiaomu Qiao ◽  
Isabelle Roth ◽  
Eric Feraille ◽  
Udo Hasler
Keyword(s):  
Cell Proliferation ◽  
Epithelial Cell ◽  
Epithelial Cell Proliferation ◽  
Hypertonic Stress ◽  
Zonula Occludens

Enteric glia inhibit intestinal epithelial cell proliferation partly through a TGF-β1-dependent pathway

2007 ◽  
Vol 292 (1) ◽  
pp. G231-G241 ◽  
Author(s):  
M. Neunlist ◽  
P. Aubert ◽  
S. Bonnaud ◽  
L. Van Landeghem ◽  
E. Coron ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Epithelial Cell ◽  
Cell Density ◽  
Intestinal Epithelial Cell ◽  
Intestinal Barrier ◽  
Intestinal Epithelial ◽  
Epithelial Cell Proliferation ◽  
Coculture Model

Although recent studies have shown that enteric neurons control intestinal barrier function, the role of enteric glial cells (EGCs) in this control remains unknown. Therefore, our goal was to characterize the role of EGCs in the control of intestinal epithelial cell proliferation using an in vivo transgenic and an in vitro coculture model. Assessment of intestinal epithelial cell proliferation after ablation of EGCs in transgenic mice demonstrated a significant increase in crypt cell hyperplasia. Furthermore, mucosal glial network (assessed by immunohistochemical detection of S-100β) is altered in colon adenocarcinoma compared with control tissue. In an in vitro coculture model of subconfluent Caco-2 cells seeded onto Transwell filters with EGCs, Caco-2 cell density and [3H]thymidine incorporation were significantly lower than in control (Caco-2 cultured alone). Flow cytometry analysis showed that EGCs had no effect on Caco-2 cell viability. EGCs induced a significant increase in Caco-2 cell surface area without any sign of cellular hypertrophy. These effects by EGCs were also seen in various transformed or nontransformed intestinal epithelial cell lines. Furthermore, TGF-β1 mRNA was expressed, and TGF-β1 was secreted by EGCs. Exogenously added TGF-β1 reproduced partly the EGC-mediated effects on cell density and surface area. In addition, EGC effects on Caco-2 cell density were significantly reduced by a neutralizing TGF-β antibody. In conclusion, EGCs have profound antiproliferative effects on intestinal epithelial cells. Functional alterations in EGCs may therefore modify intestinal barrier functions and be involved in pathologies such as cancer or inflammatory bowel diseases.

scholarly journals Evaluation of the Role of Candida albicans Agglutinin-Like Sequence (Als) Proteins in Human Oral Epithelial Cell Interactions

PLoS ONE ◽  
2012 ◽  
Vol 7 (3) ◽  
pp. e33362 ◽  
Author(s):  
Celia Murciano ◽  
David L. Moyes ◽  
Manohursingh Runglall ◽  
Priscila Tobouti ◽  
Ayesha Islam ◽  
...  
Keyword(s):  
Candida Albicans ◽  
Epithelial Cell ◽  
Cell Interactions ◽  
Oral Epithelial Cell ◽  
Oral Epithelial ◽  
Human Oral Epithelial Cell
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