• Je něco špatně v tomto záznamu ?

Expression of genes responsible for cell morphogenesis involved in differentiation in porcine buccal pouch mucosal cells during long-term primary culture and real-time proliferation in vitro

M. Dyszkiewicz-Konwińska, A. Bryja, K. Jopek, J. Budna, R. Khozmi, M. Jeseta, D. Bukowska, P. Antosik, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,

. 2017 ; 31 (4) : 855-864.

Jazyk angličtina Země Itálie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18010236

Recently, using experimental animal model, we demonstrated that porcine buccal pouch mucosal cells reflect increased proliferation capability during primary cultivation in vitro. Although the histological structure and morphogenesis in oral cavity is well recognized, the molecular mechanisms which regulate this process still need further investigation. This study was aimed to analyze the molecular marker expression profile involved in morphogenesis and differentiation capacity of porcine buccal pouch mucosal cells during their long-term primary cultivation in vitro. The experiment was performed on buccal pouch mucosal cells isolated from 80 pubertal crossbred Landrace gilts. After collection, the cells were treated enzymatically and transferred into a primary in vitro culture (IVC) system and cultured for 30 days. The cells were collected for RNA isolation after 7, 15 and 30 days of IVC and were checked for their real-time proliferative status using the RTCA system. We found an increased expression of FN1 and SOX9 genes when calculated against ACTB after 7, and 30 days of IVC, (P less than 0.01, P less than 0.001, respectively). The CXCL12 mRNA was down-regulated after 7, 15 and 30 days of IVC, but not statistically significant. Similar expression profile was observed when calculated against HPRT, however, DAB2 was found to be higher expressed at day 15 of IVC, (P less than 0.05). The cell index measured during real-time cell proliferation was substantially increased between 96 h and 147h of IVC and reached the log phase. Since FN1 and SOX9 revealed significant increase of expression after long-term culture in vitro, it is suggested that expression of these differentiation and stemness genes is accompanied by cell proliferation. Moreover, FN1 and SOX9 might be recognized as new markers of buccal pouch mucosal cell proliferation and differentiation in pigs in in vitro primary culture model.

000      
00000naa a2200000 a 4500
001      
bmc18010236
003      
CZ-PrNML
005      
20180416092954.0
007      
ta
008      
180404s2017 it f 000 0|eng||
009      
AR
035    __
$a (PubMed)29254288
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a it
100    1_
$a Dyszkiewicz-Konwińska, M $u Department of Biomaterials and Experimental Dentistry, Poznań University of Medical Sciences, Poznań, Poland.
245    10
$a Expression of genes responsible for cell morphogenesis involved in differentiation in porcine buccal pouch mucosal cells during long-term primary culture and real-time proliferation in vitro / $c M. Dyszkiewicz-Konwińska, A. Bryja, K. Jopek, J. Budna, R. Khozmi, M. Jeseta, D. Bukowska, P. Antosik, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,
520    9_
$a Recently, using experimental animal model, we demonstrated that porcine buccal pouch mucosal cells reflect increased proliferation capability during primary cultivation in vitro. Although the histological structure and morphogenesis in oral cavity is well recognized, the molecular mechanisms which regulate this process still need further investigation. This study was aimed to analyze the molecular marker expression profile involved in morphogenesis and differentiation capacity of porcine buccal pouch mucosal cells during their long-term primary cultivation in vitro. The experiment was performed on buccal pouch mucosal cells isolated from 80 pubertal crossbred Landrace gilts. After collection, the cells were treated enzymatically and transferred into a primary in vitro culture (IVC) system and cultured for 30 days. The cells were collected for RNA isolation after 7, 15 and 30 days of IVC and were checked for their real-time proliferative status using the RTCA system. We found an increased expression of FN1 and SOX9 genes when calculated against ACTB after 7, and 30 days of IVC, (P less than 0.01, P less than 0.001, respectively). The CXCL12 mRNA was down-regulated after 7, 15 and 30 days of IVC, but not statistically significant. Similar expression profile was observed when calculated against HPRT, however, DAB2 was found to be higher expressed at day 15 of IVC, (P less than 0.05). The cell index measured during real-time cell proliferation was substantially increased between 96 h and 147h of IVC and reached the log phase. Since FN1 and SOX9 revealed significant increase of expression after long-term culture in vitro, it is suggested that expression of these differentiation and stemness genes is accompanied by cell proliferation. Moreover, FN1 and SOX9 might be recognized as new markers of buccal pouch mucosal cell proliferation and differentiation in pigs in in vitro primary culture model.
650    _2
$a zvířata $7 D000818
650    _2
$a buněčná diferenciace $7 D002454
650    _2
$a proliferace buněk $7 D049109
650    _2
$a chemokin CXCL12 $x genetika $x metabolismus $7 D054377
650    _2
$a epitelové buňky $x cytologie $x metabolismus $7 D004847
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a stanovení celkové genové exprese $7 D020869
650    12
$a vývojová regulace genové exprese $7 D018507
650    _2
$a hypoxanthinfosforibosyltransferasa $x genetika $x metabolismus $7 D007041
650    _2
$a lipokalin-2 $x genetika $x metabolismus $7 D000071068
650    _2
$a morfogeneze $x genetika $7 D009024
650    _2
$a ústní sliznice $x cytologie $x růst a vývoj $x metabolismus $7 D009061
650    _2
$a primární buněčná kultura $7 D061251
650    _2
$a messenger RNA $x genetika $x metabolismus $7 D012333
650    _2
$a transkripční faktor SOX9 $x genetika $x metabolismus $7 D055758
650    _2
$a signální transdukce $7 D015398
650    _2
$a prasata $7 D013552
650    _2
$a nádorové supresorové proteiny $x genetika $x metabolismus $7 D025521
655    _2
$a časopisecké články $7 D016428
700    1_
$a Bryja, A $u Department of Anatomy, Poznań University of Medical Science, Poznań, Poland.
700    1_
$a Jopek, K $u Department of Histology and Embryology, Poznań University of Medical Science, Poznań, Poland.
700    1_
$a Budna, J $u Department of Histology and Embryology, Poznań University of Medical Science, Poznań, Poland.
700    1_
$a Khozmi, R $u Department of Anatomy, Poznań University of Medical Science, Poznań, Poland.
700    1_
$a Jeseta, M $u Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Brno, Czech Republic.
700    1_
$a Bukowska, D $u Institute of Veterinary, Poznań University of Life Sciences, Poznań, Poland.
700    1_
$a Antosik, P $u Institute of Veterinary, Poznań University of Life Sciences, Poznań, Poland.
700    1_
$a Bruska, M $u Department of Biomaterials and Experimental Dentistry, Poznań University of Medical Sciences, Poznań, Poland.
700    1_
$a Nowicki, M $u Department of Histology and Embryology, Poznań University of Medical Science, Poznań, Poland.
700    1_
$a Zabel, M $u Department of Histology and Embryology, Poznań University of Medical Science, Poznań, Poland. Department of Histology and Embryology, Wroclaw Medical University, Wroclaw, Poland.
700    1_
$a Kempisty, B $u Department of Anatomy, Poznań University of Medical Science, Poznań, Poland. Department of Histology and Embryology, Poznań University of Medical Science, Poznań, Poland. Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Brno, Czech Republic.
773    0_
$w MED00008336 $t Journal of biological regulators & homeostatic agents $x 0393-974X $g Roč. 31, č. 4 (2017), s. 855-864
856    41
$u https://pubmed.ncbi.nlm.nih.gov/29254288 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180404 $b ABA008
991    __
$a 20180416093051 $b ABA008
999    __
$a ok $b bmc $g 1287721 $s 1007048
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 31 $c 4 $d 855-864 $i 0393-974X $m Journal of Biological Regulators & Homeostatic Agents $n J Biol Regul Homeost Agents $x MED00008336
LZP    __
$a Pubmed-20180404

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace