scholarly journals cDNA cloning of rat pS2 peptide and expression of trefoil peptides in acetic acid-induced colitis

1996 ◽  
Vol 318 (3) ◽  
pp. 939-944 ◽  
Author(s):  
Hiroshi ITOH ◽  
Masaki TOMITA ◽  
Hirofumi UCHINO ◽  
Takahiko KOBAYASHI ◽  
Hiroaki KATAOKA ◽  
...  

By using a combination of the methods of reverse transcription-PCR and rapid amplification of cDNA ends, a cDNA for rat pS2 peptide (rpS2) was successfully cloned and sequenced from rat stomach. By RNA blot analysis, the gene was shown to be expressed abundantly in the stomach and only faintly in the duodenum, but not in other tissues including the distal small and large intestines. rpS2 expression was also examined in the rectum during the course of acetic acid-induced colitis; rpS2 mRNA was detected during the acute phase of colitis but not in normal controls or during the recovery phase. On the other hand, expression of rat intestinal trefoil factor (rITF) was down-regulated during the acute phase of colitis and then up-regulated during the recovery phase, whereas rat spasmolytic peptide was not detectable throughout the course of the induced colitis. These results indicate that the patterns and timing of the expression of these trefoil peptides are different from each other. rpS2 may play an important role in the proliferation of intestinal epithelial cells during the acute phase of mucosal ulceration, whereas rITF may be involved in differentiation of the cells, particularly to form goblet cells, during the recovery phase.

1995 ◽  
Vol 311 (1) ◽  
pp. 293-297 ◽  
Author(s):  
M Tomita ◽  
H Itoh ◽  
N Ishikawa ◽  
A Higa ◽  
H Ide ◽  
...  

A cDNA encoding mouse intestinal trefoil factor (mITF) was successfully cloned and sequenced from the small intestine of C57BL/6 mouse by using the combination of reverse transcription-PCR and rapid amplification of cDNA ends methods. The gene was, similar to rat and human ITFs, mainly expressed in the small and large intestine. The mITF expression was up-regulated during the recovery phase after depletion of goblet cells in acetic acid-induced colitis. On the other hand, the expression in the jejunum was not altered, while goblet cell hyperplasia was induced by Nippostrongylus brasiliensis infection. These results suggest that the mITF expression did not simply correlate with the number of goblet cells. The mITF may play an important role in the maintenance and repair of mucosal function of the rectum. Additionally, the mITF in the jejunum may play a role in alteration of the physicochemical nature of goblet cell mucins, thereby affecting the establishment of intestinal helminths.


1999 ◽  
Vol 45 (4, Part 2 of 2) ◽  
pp. 208A-208A
Author(s):  
Jing Lin ◽  
Ian R Holzman ◽  
Hikaru Kozuma ◽  
Taral Patel ◽  
Ping Jiang ◽  
...  

2015 ◽  
Vol 23 (8) ◽  
pp. 1290
Author(s):  
Xue Lin ◽  
Zhi-Feng Liu ◽  
Yu-Hua Ding ◽  
Fan Wang ◽  
Hua-Qin Pan ◽  
...  

FEBS Letters ◽  
1995 ◽  
Vol 357 (1) ◽  
pp. 50-54 ◽  
Author(s):  
Rebecca Chinery ◽  
Paul A. Bates ◽  
Amitabha De ◽  
Paul S. Freemont

1992 ◽  
Vol 285 (1) ◽  
pp. 5-8 ◽  
Author(s):  
R Chinery ◽  
R Poulsom ◽  
L A Rogers ◽  
R E Jeffery ◽  
J M Longcroft ◽  
...  

A cDNA encoding rat intestinal trefoil factor (rITF) was prepared by reverse transcription and PCR amplification. The sequence obtained was well conserved with that of other trefoil peptides. An antisense riboprobe produced from the clone was used to localize the sites of ITF expression in the rat gastrointestinal tract using hybridization in situ. We found rITF mRNA in goblet cells in the small intestine and colon; a gradient of signal strength greatest near the crypt base was sometimes present. We found no evidence for rITF expression in Brunner's glands, the pancreas, or most regions of the gastric mucosa. Surprisingly, strong signals for rITF mRNA were detected in a region of stomach at the junction of the squamous fore-stomach with the glandular gastric mucosa. This region, which may correspond to the cardiac region, formed part of a larger area of cells staining positive for acid mucins. We hypothesize that concerted expression occurs of particular trefoil peptides with specific mucins, and that this organization reflects a functional relationship between mucins and trefoil peptides.


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