-
Something wrong with this record ?
Brain-derived neurotrophic factor modulates intestinal barrier by inhibiting intestinal epithelial cells apoptosis in mice
D. Y. Zhao, W. X. Zhang, Q. Q. Qi, X. Long, X. Li, Y. B. Yu, X. L. Zuo,
Language English Country Czech Republic
Document type Journal Article
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Apoptosis * MeSH
- Epithelial Cells physiology MeSH
- Caspase 3 metabolism MeSH
- Brain-Derived Neurotrophic Factor physiology MeSH
- Mice, Inbred C57BL MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Tight Junction Proteins metabolism MeSH
- Intestinal Mucosa metabolism ultrastructure MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
We aimed to investigate the effects of brain-derived neurotrophic factor (BDNF) on apoptosis of intestinal epithelial cells (IECs) and alterations of intestinal barrier integrity using BDNF knock-out mice model. Colonic tissues from BDNF(+/+) mice and BDNF(+/-) mice were prepared for this study. The integrity of colonic mucosa was evaluated by measuring trans-mucosa electrical resistance and tissue conductance in Ussing chamber. The colonic epithelial structure was analyzed by transmission electron microscopy. Apoptosis involvement was determined with TUNEL staining, active caspase-3 immunostaining and Western blotting for the protein expression of active caspase-3, Bax and Bcl-2. The expression levels and distribution of tight junction proteins were evaluated by immunohistochemistry or Western blots. Compared with BDNF(+/+) mice, BDNF(+/-) mice displayed impaired integrity and ultrastructure alterations in their colonic mucosa, which was characterized by diminished microvilli, mitochondrial swelling and epithelial cells apoptosis. Altered intestinal barrier function was linked to excessive apoptosis of IECs demonstrated by the higher proportion of TUNEL-positive apoptotic cells and enhanced caspase activities in BDNF(+/-) mice. Increased expression of Bax and claudin-2 proteins and reduced Bcl-2 and tight junction proteins (occludin, ZO-1 and claudin-1) expression were also detected in the colonic mucosa of BDNF(+/-) mice. BDNF may play a role in the maintenance of intestinal barrier integrity via its anti-apoptotic properties.
Department of Gastroenterology Puyang Oilfield General Hospital Puyang China
Department of Gastroenterology Qilu Hospital Shandong University Jinan China
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18040230
- 003
- CZ-PrNML
- 005
- 20190122094537.0
- 007
- ta
- 008
- 181214s2018 xr ad f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.933641 $2 doi
- 035 __
- $a (PubMed)29527912
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Zhao, D. Y. $u Department of Gastroenterology, Puyang Oilfield General Hospital, Puyang, China
- 245 10
- $a Brain-derived neurotrophic factor modulates intestinal barrier by inhibiting intestinal epithelial cells apoptosis in mice / $c D. Y. Zhao, W. X. Zhang, Q. Q. Qi, X. Long, X. Li, Y. B. Yu, X. L. Zuo,
- 520 9_
- $a We aimed to investigate the effects of brain-derived neurotrophic factor (BDNF) on apoptosis of intestinal epithelial cells (IECs) and alterations of intestinal barrier integrity using BDNF knock-out mice model. Colonic tissues from BDNF(+/+) mice and BDNF(+/-) mice were prepared for this study. The integrity of colonic mucosa was evaluated by measuring trans-mucosa electrical resistance and tissue conductance in Ussing chamber. The colonic epithelial structure was analyzed by transmission electron microscopy. Apoptosis involvement was determined with TUNEL staining, active caspase-3 immunostaining and Western blotting for the protein expression of active caspase-3, Bax and Bcl-2. The expression levels and distribution of tight junction proteins were evaluated by immunohistochemistry or Western blots. Compared with BDNF(+/+) mice, BDNF(+/-) mice displayed impaired integrity and ultrastructure alterations in their colonic mucosa, which was characterized by diminished microvilli, mitochondrial swelling and epithelial cells apoptosis. Altered intestinal barrier function was linked to excessive apoptosis of IECs demonstrated by the higher proportion of TUNEL-positive apoptotic cells and enhanced caspase activities in BDNF(+/-) mice. Increased expression of Bax and claudin-2 proteins and reduced Bcl-2 and tight junction proteins (occludin, ZO-1 and claudin-1) expression were also detected in the colonic mucosa of BDNF(+/-) mice. BDNF may play a role in the maintenance of intestinal barrier integrity via its anti-apoptotic properties.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a apoptóza $7 D017209
- 650 _2
- $a mozkový neurotrofický faktor $x fyziologie $7 D019208
- 650 _2
- $a kaspasa 3 $x metabolismus $7 D053148
- 650 _2
- $a epitelové buňky $x fyziologie $7 D004847
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a střevní sliznice $x metabolismus $x ultrastruktura $7 D007413
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a myši knockoutované $7 D018345
- 650 _2
- $a proteiny těsného spoje $x metabolismus $7 D062725
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Zhang, W. X. $u Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China
- 700 1_
- $a Qi, Q. Q. $u Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China
- 700 1_
- $a Long, X. $u Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China
- 700 1_
- $a Li, X. $u Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China
- 700 1_
- $a Yu, Y. B. $u Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China
- 700 1_
- $a Zuo, X. L. $u Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 67, č. 3 (2018), s. 475-485
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/29527912 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20181214 $b ABA008
- 991 __
- $a 20190109131231 $b ABA008
- 999 __
- $a ok $b bmc $g 1369653 $s 1037293
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 67 $c 3 $d 475-485 $e 20180312 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $b NLK118 $a Pubmed-20181214