中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2012年
9期
638-641
,共4页
秦委委%张岚%张纪蔚%张柏根%何以丰%陈春妹%余龙
秦委委%張嵐%張紀蔚%張柏根%何以豐%陳春妹%餘龍
진위위%장람%장기위%장백근%하이봉%진춘매%여룡
受体,趋化因子%静脉%炎症%白细胞介素8%Duffy抗原
受體,趨化因子%靜脈%炎癥%白細胞介素8%Duffy抗原
수체,추화인자%정맥%염증%백세포개소8%Duffy항원
Receptors,chemokines%Veins%Inflammation%Interleukin-8%Duffy antigen
目的 探讨组织间Duffy抗原/趋化因子受体(DARC)在下肢静脉高压炎症反应中的作用及其可能的机制.方法 采用股动-静脉瘘建立大鼠后肢静脉高压模型,36只SD大鼠数字随机分为pcDNA3.1-DARC质粒组、pcDNA3.1空质粒组和对照组.术后14 d和42 d,采用实时定量聚合酶链反应(Real-PCR)和蛋白印迹(Western blotting)检测组织间DARC mRNA和蛋白的表达;酶联免疫吸附测定法检测血清白细胞介素(IL)-8的含量;TUNEL法和HE染色检测组织凋亡和白细胞浸润情况.结果 随着静脉高压时间的延长,组织间DARC表达量、组织凋亡及白细胞浸润程度在pcDNA3.1-DARC质粒组和pcDNA3.1空质粒组均呈增加的趋势,同期各组间比较,pcDNA3.1-DARC质粒组明显高于pcDNA3.1空质粒组和对照组,差异均有统计学意义(均P<0.05);血清IL-8含量在pcDNA3.1-DARC质粒组和pcDNA3.1空质粒组均表现为降低的趋势,同期各组间比较,pcDNA3.-DARC质粒组明显低于pcDNA3.1空质粒组,但两组均高于对照组,差异均有统计学意义(均P<0.05).结论 组织间DARC表达与静脉高压组织的炎症程度呈正相关,可能通过加强白细胞的黏附和迁移促进静脉高压炎症反应的发展.
目的 探討組織間Duffy抗原/趨化因子受體(DARC)在下肢靜脈高壓炎癥反應中的作用及其可能的機製.方法 採用股動-靜脈瘺建立大鼠後肢靜脈高壓模型,36隻SD大鼠數字隨機分為pcDNA3.1-DARC質粒組、pcDNA3.1空質粒組和對照組.術後14 d和42 d,採用實時定量聚閤酶鏈反應(Real-PCR)和蛋白印跡(Western blotting)檢測組織間DARC mRNA和蛋白的錶達;酶聯免疫吸附測定法檢測血清白細胞介素(IL)-8的含量;TUNEL法和HE染色檢測組織凋亡和白細胞浸潤情況.結果 隨著靜脈高壓時間的延長,組織間DARC錶達量、組織凋亡及白細胞浸潤程度在pcDNA3.1-DARC質粒組和pcDNA3.1空質粒組均呈增加的趨勢,同期各組間比較,pcDNA3.1-DARC質粒組明顯高于pcDNA3.1空質粒組和對照組,差異均有統計學意義(均P<0.05);血清IL-8含量在pcDNA3.1-DARC質粒組和pcDNA3.1空質粒組均錶現為降低的趨勢,同期各組間比較,pcDNA3.-DARC質粒組明顯低于pcDNA3.1空質粒組,但兩組均高于對照組,差異均有統計學意義(均P<0.05).結論 組織間DARC錶達與靜脈高壓組織的炎癥程度呈正相關,可能通過加彊白細胞的黏附和遷移促進靜脈高壓炎癥反應的髮展.
목적 탐토조직간Duffy항원/추화인자수체(DARC)재하지정맥고압염증반응중적작용급기가능적궤제.방법 채용고동-정맥루건립대서후지정맥고압모형,36지SD대서수자수궤분위pcDNA3.1-DARC질립조、pcDNA3.1공질립조화대조조.술후14 d화42 d,채용실시정량취합매련반응(Real-PCR)화단백인적(Western blotting)검측조직간DARC mRNA화단백적표체;매련면역흡부측정법검측혈청백세포개소(IL)-8적함량;TUNEL법화HE염색검측조직조망화백세포침윤정황.결과 수착정맥고압시간적연장,조직간DARC표체량、조직조망급백세포침윤정도재pcDNA3.1-DARC질립조화pcDNA3.1공질립조균정증가적추세,동기각조간비교,pcDNA3.1-DARC질립조명현고우pcDNA3.1공질립조화대조조,차이균유통계학의의(균P<0.05);혈청IL-8함량재pcDNA3.1-DARC질립조화pcDNA3.1공질립조균표현위강저적추세,동기각조간비교,pcDNA3.-DARC질립조명현저우pcDNA3.1공질립조,단량조균고우대조조,차이균유통계학의의(균P<0.05).결론 조직간DARC표체여정맥고압조직적염증정도정정상관,가능통과가강백세포적점부화천이촉진정맥고압염증반응적발전.
Objective To explore the role and mechanism of Duffy antigen receptor for chemokines (DARC) of tissue in promoting the inflammatory reaction of the limb with venous hypertension.Methods Femoral arteriovenous fistula was surgically created to establish the rat model of venous hypertension.A total of 36 SD rats were randomly divided into pcDNA3.1-DARC ( Group A),empty plasmid of pcDNA3.1 (Group B) and control (Group C) groups.The animals were sacrificed at Days 14 and 42 post-operation respectively.The expressions of DARC at the RNA and protein level were detected by real-time polymerase chain reaction (Real-PCR) and Western blotting.And the serum level of interleukin (IL)-8 was detected by enzyme linked immunosorbent assay (ELISA) and the degrees of apoptosis and leukocytic infiltration of local tissue were detected by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) and hematoxylin and eosin (HE) staining.Results With the elapsing time of venous hypertension,the DARC expression in tissue,the extent of apoptosis and leukocytic infiltration in tissue showed an increasing trend in Groups A and B.Group A was obviously higher than Group B during the corresponding period.And the differences were statistically significant (P < 0.05).The serum levels of IL-8 of Groups A and B showed a decreasing trend.And Group A was obviously lower than Group B. Both groups were higher than the control group. The differences were statistically significant ( P < 0.05 ).Conclusion The level of DARC in tissue and the degree of inflammatory reaction of venous hypertension have a positive correlation.And DARC may promote the development of venous hypertension inflammation through augmenting the adhesion and migration of leukocytes.