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01000naa a22002652 4500 |
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NLM252192508 |
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DE-627 |
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20231224163612.0 |
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tu |
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231224s2015 xx ||||| 00| ||chi c |
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|a pubmed24n0840.xml
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|a (DE-627)NLM252192508
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| 035 |
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|a (NLM)26310643
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| 040 |
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|a DE-627
|b ger
|c DE-627
|e rakwb
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| 041 |
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|a chi
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| 100 |
1 |
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|a Li, Wei
|e verfasserin
|4 aut
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| 245 |
1 |
0 |
|a Tight junction protein expression of gastric mucosa and its significance in children with Helicobacter pylori infection
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| 264 |
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1 |
|c 2015
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| 336 |
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|a Text
|b txt
|2 rdacontent
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| 337 |
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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| 338 |
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|a Band
|b nc
|2 rdacarrier
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| 500 |
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|a Date Completed 22.01.2016
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| 500 |
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|a Date Revised 02.12.2018
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| 500 |
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|a published: Print
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| 500 |
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|a Citation Status MEDLINE
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| 520 |
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|a OBJECTIVE: To understand the junction protein expression of gastric mucosa including occlusal proteins (occludin), closed protein-4 (claudin-4), zonula occluden-1(ZO-1), epithelial cadherin (E-cadherin), and β ring protein (β-catenin) and the clinical significance in children with Helicobacter pylori (Hp) infection
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| 520 |
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|a METHOD: Seventy patients in whom gastric endoscopy was performed because of nausea, vomiting, abdominal pain, bloating, acid reflux, melena, and other gastrointestinal symptoms were enrolled in this study from Dec. 2010 to Apr. 2013 in our hospital. Informed consent was signed by their parents, and the study was in accordance with the principles of medical ethics. Hp positivity was confirmed if both respiratory urea test (RUT) and Hp were positive by gastric mucosal pathology. Gastric mucosal samples from 70 patients were enrolled in this study, 23 of them were Hp negative, 47 of them were Hp positive (24 cases without peptic ulcer, 23 cases with peptic ulcer). The mRNA levels and protein expression of tight junction protein of gastric mucosa were measured by RT-PCR and Western blot respectively. The location and semi quantitative content of E-cadherin and β-catenin in gastric mucosa were detected by immunohistochemical staining method
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| 520 |
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|a RESULT: The mRNA level of E-cadherin, β-catenin, ZO-1 in the Hp positive group regardless of peptic ulcer was significantly lower than that in the Hp negative group. Hp positive without peptic ulcer group were 0.0008, 0.0040, 0.0014, respectively; Hp positive with peptic ulcer group were 0.0010, 0.0090, 0.0013, respectively; Hp negative group were 0.0137, 0.0423, 0.0198, respectively (F values were 36.956, 39.893, 38.962, respectively, all P<0.05). The expression of claudin-4 mRNA in Hp positive group with peptic ulcer increased significantly, the difference among Hp positive group with peptic ulcer, Hp positive group without peptic ulcer and Hp negative group was statistically significant (0.1438 vs. 0.0926 vs. 0.0789) (F value was 11.964, P<0.05), while the difference of occludin mRNA levels among the three groups was not statistically significant.Immunohistochemistry results showed that the score of E-cadherin, β-catenin positive cell in the Hp positive patients were also significantly lower than that in the Hp negative group (t values were 3.981 and 2.340, all P<0.05, respectively). Western blot results showed that the protein levels of β-catenin in Hp positive group with peptic ulcer were significantly lower than that in Hp negative group, while the protein levels of E-cadherin in Hp positive patients regardless of peptic ulcer were decreased significantly in Hp negative group
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| 520 |
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|a CONCLUSION: Our results revealed that the tight junction protein E-cadherin, β-catenin, ZO-1 expression of gastric mucosa were decreased in children with Hp infection, while claudin-4 expression was increased in Hp positive patients with peptic ulcer, suggesting that damage to gastric epithelial barrier function may be the main pathogenesis of Hp associated gastric diseases in children
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| 650 |
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4 |
|a Journal Article
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| 650 |
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7 |
|a Antigens, CD
|2 NLM
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| 650 |
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7 |
|a CDH1 protein, human
|2 NLM
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| 650 |
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7 |
|a CLDN4 protein, human
|2 NLM
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| 650 |
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7 |
|a CTNNB1 protein, human
|2 NLM
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| 650 |
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7 |
|a Cadherins
|2 NLM
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| 650 |
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7 |
|a Claudin-4
|2 NLM
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| 650 |
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7 |
|a OCLN protein, human
|2 NLM
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| 650 |
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7 |
|a Occludin
|2 NLM
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| 650 |
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7 |
|a RNA, Messenger
|2 NLM
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| 650 |
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7 |
|a TJP1 protein, human
|2 NLM
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| 650 |
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7 |
|a Tight Junction Proteins
|2 NLM
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| 650 |
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7 |
|a Zonula Occludens-1 Protein
|2 NLM
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| 650 |
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7 |
|a beta Catenin
|2 NLM
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| 700 |
1 |
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|a Shu, Xiaoli
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Gu, Weizhong
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Peng, Kerong
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Cai, Haifang
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Jiang, Liqin
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Jiang, Mizu
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Zhonghua er ke za zhi = Chinese journal of pediatrics
|d 1960
|g 53(2015), 7 vom: 02. Juli, Seite 510-5
|w (DE-627)NLM136249191
|x 0578-1310
|7 nnns
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| 773 |
1 |
8 |
|g volume:53
|g year:2015
|g number:7
|g day:02
|g month:07
|g pages:510-5
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| 912 |
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|a GBV_USEFLAG_A
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| 912 |
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|a SYSFLAG_A
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| 912 |
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|a GBV_NLM
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| 912 |
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|a GBV_ILN_11
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| 912 |
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|a GBV_ILN_20
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| 912 |
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|a GBV_ILN_22
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| 912 |
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|a GBV_ILN_24
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| 912 |
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|a GBV_ILN_31
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| 912 |
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|a GBV_ILN_39
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| 912 |
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|a GBV_ILN_40
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| 912 |
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|a GBV_ILN_50
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| 912 |
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|a GBV_ILN_61
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| 912 |
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|a GBV_ILN_65
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| 912 |
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|a GBV_ILN_69
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| 912 |
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|a GBV_ILN_70
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| 912 |
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|a GBV_ILN_72
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| 912 |
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|a GBV_ILN_120
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| 912 |
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|a GBV_ILN_130
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| 912 |
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|a GBV_ILN_227
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| 912 |
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|a GBV_ILN_244
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| 912 |
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|a GBV_ILN_285
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| 912 |
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|a GBV_ILN_294
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| 912 |
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|a GBV_ILN_350
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| 912 |
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|a GBV_ILN_665
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| 912 |
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|a GBV_ILN_813
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| 951 |
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|a AR
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| 952 |
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|d 53
|j 2015
|e 7
|b 02
|c 07
|h 510-5
|