• Something wrong with this record ?

PTEN and soluble epoxide hydrolase in intestinal cell differentiation

K. Koubova, K. Cizkova, A. Burianova, Z. Tauber

. 2023 ; 1867 (12) : 130496. [pub] 20231020

Language English Country Netherlands

Document type Journal Article, Research Support, Non-U.S. Gov't

Intestinal epithelial differentiation is a highly organised process. It is influenced by a variety of signalling pathways and enzymes, such as the PI3K pathway and soluble epoxide hydrolase (sEH) from arachidonic acid metabolism. We investigated the changes in the expression of enzymes and lipid messenger from the PI3K pathway, including PTEN, during intestinal cell differentiation in vitro using HT-29 and Caco2 cells and compared them with immunohistochemical patterns of these proteins in human colon. To investigate the possible crosstalk between the PI3K pathway and sEH, we treated HT-29 and Caco2 cells with the sEH inhibitor TPPU. Administration of TPPU to differentiated cells decreased the expression of PTEN, thus reversing the change in its expression observed during cell differentiation. In addition, multiplex immunofluorescence staining confirmed the relationship between the expression of PTEN and villin, a marker of intestinal cell differentiation, ranging from a moderate correlation in undifferentiated cells to a very strong correlation in differentiated cells treated with TPPU. Furthermore, we confirm that PTEN and sEH mirrored their expression patterns in samples of prenatal and adult human intestine compared to tumours using immunohistochemical staining. Taken together, it appears that PTEN and sEH cooperate in the process of intestinal cell differentiation. A better understanding of the crosstalk between the PI3K pathway and sEH and its consequences for cell differentiation is highly desirable, as several sEH inhibitors are under clinical investigation for the treatment of various diseases.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc24000395
003      
CZ-PrNML
005      
20240213093143.0
007      
ta
008      
240109s2023 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.bbagen.2023.130496 $2 doi
035    __
$a (PubMed)37866587
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Koubova, Katerina $u Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University, 779 00 Olomouc, Czech Republic
245    10
$a PTEN and soluble epoxide hydrolase in intestinal cell differentiation / $c K. Koubova, K. Cizkova, A. Burianova, Z. Tauber
520    9_
$a Intestinal epithelial differentiation is a highly organised process. It is influenced by a variety of signalling pathways and enzymes, such as the PI3K pathway and soluble epoxide hydrolase (sEH) from arachidonic acid metabolism. We investigated the changes in the expression of enzymes and lipid messenger from the PI3K pathway, including PTEN, during intestinal cell differentiation in vitro using HT-29 and Caco2 cells and compared them with immunohistochemical patterns of these proteins in human colon. To investigate the possible crosstalk between the PI3K pathway and sEH, we treated HT-29 and Caco2 cells with the sEH inhibitor TPPU. Administration of TPPU to differentiated cells decreased the expression of PTEN, thus reversing the change in its expression observed during cell differentiation. In addition, multiplex immunofluorescence staining confirmed the relationship between the expression of PTEN and villin, a marker of intestinal cell differentiation, ranging from a moderate correlation in undifferentiated cells to a very strong correlation in differentiated cells treated with TPPU. Furthermore, we confirm that PTEN and sEH mirrored their expression patterns in samples of prenatal and adult human intestine compared to tumours using immunohistochemical staining. Taken together, it appears that PTEN and sEH cooperate in the process of intestinal cell differentiation. A better understanding of the crosstalk between the PI3K pathway and sEH and its consequences for cell differentiation is highly desirable, as several sEH inhibitors are under clinical investigation for the treatment of various diseases.
650    _2
$a lidé $7 D006801
650    12
$a epoxid hydrolasy $7 D004851
650    _2
$a Caco-2 buňky $7 D018938
650    12
$a fosfatidylinositol-3-kinasy $x metabolismus $7 D019869
650    _2
$a střeva $7 D007422
650    _2
$a buněčná diferenciace $7 D002454
650    _2
$a fosfohydroláza PTEN $7 D051059
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Cizkova, Katerina $u Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University, 779 00 Olomouc, Czech Republic. Electronic address: katerina.cizkova@upol.cz
700    1_
$a Burianova, Adela $u Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University, 779 00 Olomouc, Czech Republic
700    1_
$a Tauber, Zdenek $u Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University, 779 00 Olomouc, Czech Republic
773    0_
$w MED00000717 $t Biochimica et biophysica acta. G, General subjects $x 1872-8006 $g Roč. 1867, č. 12 (2023), s. 130496
856    41
$u https://pubmed.ncbi.nlm.nih.gov/37866587 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20240109 $b ABA008
991    __
$a 20240213093140 $b ABA008
999    __
$a ok $b bmc $g 2049200 $s 1210089
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2023 $b 1867 $c 12 $d 130496 $e 20231020 $i 1872-8006 $m Biochimica et biophysica acta. G, General subjects $n Biochem Biophys Acta $x MED00000717
LZP    __
$a Pubmed-20240109

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...