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400010 重庆,重庆医科大学附属第二医院肝胆外科
[ 龚建平,E-mail:gongjianping11@126.com GONG Jianping, E-mail: gongjianping11@126.com
收稿:2018-03-26,
修回:2018-05-08,
纸质出版:2018-09-30
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徐雪松, 王孟皓, 白赫, 等. 牛磺熊去氧胆酸抑制Kupffer细胞减轻大鼠肝移植后缺血再灌注损伤[J]. 第三军医大学学报, 2018,40(18):1644-1652.
Xuesong XU, Menghao WANG, He BAI, et al. Tauroursodeoxycholic acid alleviates ischemia-reperfusion injury in liver graft following transplantation by suppressing Kupffer cell function in rats[J]. Journal of Third Military Medical University, 2018, 40(18): 1644-1652.
徐雪松, 王孟皓, 白赫, 等. 牛磺熊去氧胆酸抑制Kupffer细胞减轻大鼠肝移植后缺血再灌注损伤[J]. 第三军医大学学报, 2018,40(18):1644-1652. DOI: 10.16016/j.1000-5404.201803187.
Xuesong XU, Menghao WANG, He BAI, et al. Tauroursodeoxycholic acid alleviates ischemia-reperfusion injury in liver graft following transplantation by suppressing Kupffer cell function in rats[J]. Journal of Third Military Medical University, 2018, 40(18): 1644-1652. DOI: 10.16016/j.1000-5404.201803187.
目的
2
探讨牛磺熊去氧胆酸(tauroursodeoxycholic acid,TUDCA)减轻大鼠肝移植后肝脏缺血再灌注损伤的机制。
方法
2
分离雄性SD大鼠Kupffer细胞并培养,按不同浓度梯度给予TUDCA体外处理24 h,收集细胞上清液并提取蛋白和mRNA。共分为4组:①非活化组;②活化+0 μmol/L组;③活化+50 μmol/L组;④活化+100 μmol/L组。检测炎症因子、IRE1α/TRAF2/NF-κB通路活性、P65入核程度。雄性SD大鼠于术前3 d经腹腔注射TUDCA 400 mg·kg
-1
·d
-1
或者等量生理盐水后,建立大鼠肝移植模型,分为3组:①假手术组;②缺血再灌注组(IR组);③IR+TUDCA组。各组大鼠分别于再灌注3、6、24 h后收取肝组织标本以及血液标本,并提取Kupffer细胞中蛋白。检测肝脏病理改变、肝功能、肝细胞凋亡程度、肝脏炎症因子、Kupffer细胞中IRE1α/TRAF2/NF-κB通路活性。
结果
2
TUDCA处理活化的Kupffer细胞后,IL-1β、IL-6、TNF-α分泌减少(
P
<
0.05),并且IRE1α、TRAF2、p-IKKα、p-IκB、p-P65表达降低(
P
<
0.05),P65细胞核相对表达程度降低。TUDCA干预大鼠肝移植模型后,肝组织中气球样变性、点灶坏死,汇管区大量中性粒细胞、淋巴细胞浸润,肝血窦变窄等病理改变显著减轻,IR+TUDCA组Suzuk’s评分(2.95±0.15)较IR组(4.78±0.36)明显降低,肝功能标志物水平下降(
P
<
0.05),肝实质细胞凋亡数量减少(
P
<
0.05),IR+TUDCA组凋亡指数(29.1±12.3)较IR组(56.3±17.5)明显降低(
P
<
0.05),并且IL-1β、IL-6、TNF-α分泌减少(
P
<
0.05),Kupffer细胞中IRE1α、TRAF2、p-IKKα、p-IκB、p-P65表达降低(
P
<
0.05)。
结论
2
牛磺熊去氧胆酸能够减轻大鼠肝移植后肝脏缺血再灌注损伤程度,其机制可能是下调IRE1α/TRAF2/NF-κB通路活性抑制Kupffer细胞功能。
Objective
2
To investigate the protective effect of tauroursodeoxycholic acid (TUDCA) against ischemia-reperfusion (IR) injury in the liver graft after transplantation and explore the possible mechanism.
Methods
2
Cultured Kupffer cells from male SD rats were activated by stimulation with lipopolysaccharide (LPS) followed by treatment with TUDCA (50 or 100 μmol/L) or PBS for 24 h
and the inflammatory factors and the activity of the IRE1α/TRAF2/NF-κB pathway activity in the supernatant were detected. Male SD rats were divided into sham-operation group
IR group
and IR+TUDCA group (
n
=15)
and in the latter 2 groups
the rats were subjected to daily intraperitoneal injection of normal saline and TUDCA (400 mg/kg) for 3 consecutive days
respectively
before orthotopic liver transplantation was performed. Blood and liver graft samples were collected from the recipient rats at 3
6
and 24 h after the operation for assessing the graft pathologies
liver function
hepatocyte apoptosis and the proinflammatory factors
and Kupffer cells were isolated to detect the activity of the IRE1α/TRAF2/NF-κB pathway.
Results
2
Treatment with TUDCA significantly decreased the secretion of IL-1β
IL-6 and TNF-α (
P
<
0.05)
lowered the expression levels of IRE1α
TRAF2
p-IKKα
p-IκB
and p-P65 (
P
<
0.05)
and reduced intranuclear expression of P65 in LPS-activated Kupffer cells. In the rat models of orthotopic liver transplantation
compared with saline treatment
TUDCA treatment obviously alleviated IR-induced pathologies (including ballooning degeneration
spotted and focal necrosis
massive accumalation of neutrophils in portal area
lymphocyte infiltration
and narrowing of hepatic sinuses) in the liver graft
significantly lowered the Suzuk's score from 4.78±0.36 to 2.95±0.15 (
P
<
0.05)
and reduced the levels of alanine aminotransferase and aspartate transaminase (
P
<
0.05) and hepatocyte apoptosis (
P
<
0.05). TUDCA treatment significantly lowered the apoptotic index of the graft from 56.3±17.
5 (in saline-treated IR rats) to 29.1±12.3 (
P
<
0.05)
and obviously suppressed the secretion of IL-1β
IL-6
and TNF-α (
P
<
0.05) and the expression levels of IRE1α
TRAF2
p-IKKα
p-IκB
and p-P65 (
P
<
0.05) in the Kupffer cells from the recipient rats.
Conclusion
2
TUDCA can effectively alleviate IR injury in the liver graft possibly by down-regulating the activity of IRE1α/TRAF2/NF-κB pathway to suppress the function of the Kupffer cells.
OGAWS K, KONDO T, TAMURA T, et al . Influence of Kupffer cells and platelets on ischemia-reperfusion injury in mild steatotic liver[J ] . World J Gastroenterol, 2013, 19(9): 1396-1404. DOI: 10.3748/wjg.v19.i9.1396.
WU Y, ZHANG W, LI M, et al . Nobiletin ameliorates ischemia- reperfusion injury by suppressing the function of Kupffer cells after liver transplantation in rats[J ] . Biomed Pharmacother, 2017, 89: 732-741. DOI: 10.1016/j.biopha. 2017.02.087.
BANAN B, XIAO Z, WATSON R, et al . Novel strategy to decrease reperfusion injuries and improve function of cold-preserved livers using normothermic ex vivo liver perfusion machine[J ] . Liver Transpl, 2016, 22(3): 333-343. DOI: 10.1002/lt.24352.
PARK J K, SHAO M, KIM M Y, et al . An endoplasmic reticulum protein, Nogo-B, facilitates alcoholic liver disease through regulation of kupffer cell polarization[J ] . Hepatology, 2017, 65(5): 1720-1734. DOI:10.1002/hep.29051.
GAO J, JIANG Z, WANG S, et al . Endoplasmic reticulum stress of Kupffer cells involved in the conversion of natural regulatory T cells to Th17 cells in liver ischemia-reperfusion injury[J ] . J Gastroenterol Hepatol, 2016, 31(4): 883-889. DOI: 10.1111/jgh.13163.
RAO J, YUE S, FU Y, et al . ATF6 mediates a pro-inflammatory synergy between ER stress and TLR activation in the pathogenesis of liver ischemia-reperfusion injury[J ] . Am J Transplant, 2014, 14(7): 1552-1561. DOI: 10.1111/ajt.12711.
CELLI J, TSOLIS R M. Bacteria, the endoplasmic reticulum and the unfolded protein response: friends or foes[J]. Nat Rev Microbiol, 2015, 13(2): 71-82. DOI: 10.1038/nrmicro3393.
KEESTRA-GOUNDER A M, BYNDLOSS M X, Seyffert N, et al . NOD1 and NOD2 signalling links ER stress with inflammation[J ] . Nature, 2016, 532(7599): 394-397. DOI: 10.1038/nature17631.
SAKAI N, VANSWERINGEN H L, SCHUSTER R, et al . Receptor activator of nuclear factor-κB ligand (RANKL) protects against hepatic ischemia/reperfusion injury in mice[J ] . Hepatology, 2012, 55(3): 888-897. DOI: 10.1002/hep.24756.
LAUNAY N, RUIZ M, GRAU L, et al . Tauroursodeoxycholic bile acid arrests axonal degeneration by inhibiting the unfolded protein response in X-linked adrenoleukodystrophy[J ] .Acta Neuropathol, 2017, 133(2): 283-301. DOI: 10.1007/s00401- 016-1655-9.
SUN D, GU G, WANG J, et al . Administration of tauroursodeoxycholic acid attenuates early brain injury via Akt pathway activation[J ] . Front Cell Neurosci, 2017, 11: 193. DOI: 10.3389/fncel.2017.00193.
YOON Y M, LEE J H, YUN S P, et al . Tauroursodeoxycholic acid reduces ER stress by regulating of Akt-dependent cellular prion protein[J ] . Sci Rep, 2016, 6: 39838. DOI: 10.1038/srep39838.
UPPALA J K, GANI A R, RAMAIAH KVA. Chemical chaperone, TUDCA unlike PBA, mitigates protein aggregation efficiently and resists ER and non-ER stress induced HepG2 cell death[J]. Sci Rep, 2017, 7(1):3831. DOI: 10.1038/s41598-017-03940-1.
LI P Z, LI J Z, LI M, et al . An efficient method to isolate and culture mouse Kupffer cells[J ] . Immunol Lett, 2014, 158(1-2): 52-56. DOI: 10.1016/j.imlet.2013.12.002.
WU Y, WANG Y, LI M, et al . Gadolinium chloride suppresses acute rejection and induces tolerance following rat liver transplantation by inhibiting Kupffer-cell activation[J ] . Exp Ther Med, 2014, 8(6): 1777-1782. DOI: 10.3892/etm.2014. 2015.
ZHANG Y Q, DING N, ZENG Y F, et al . New progress in roles of nitric oxide during hepatic ischemia reperfusion injury[J ] .World J Gastroenterol, 2017, 23(14): 2505-2510. DOI: 10.3748/wjg.v23.i14.2505.
GROOTJANS J, KASER A, KAUFMAN R J, et al .The unfolded protein response in immunity and inflammation[J ] . Nat Rev Immunol, 2016, 16(8): 469-484. DOI: 10.1038/nri.2016.62.
SHAH A, KUMAR A. Methamphetamine-mediated endoplasmic reticulum (ER) stress induces type-1 programmed cell death in astrocytes via ATF6, IRE1αand PERK pathways[J]. Oncotarget, 2016, 7(29): 46100-46119. DOI: 10.18632/oncotarget.10025.
BROWN M, STRUDWICK N, SUWARA M, et al . An initial phase of JNK activation inhibits cell death early in the endoplasmic reticulum stress response[J ] . J Cell Sci, 2016, 129(12): 2317-2328. DOI: 10.1242/jcs.179127.
SU C C. Tanshinone IIA could inhibit pancreatic cancer BxPC-3 cells through increasing PERK, ATF6, caspase-12 and CHOP expression to induce apoptosis[J]. J Bio Sci Eng, 2015, 8(3): 149-159.
IMARISIO C, ALCHERA E, Bangalore Revanna C, et al . Oxidative and ER stress-dependent ASK1 activation in steatotic hepatocytes and Kupffer cells sensitizes mice fatty liver to ischemia/reperfusion injury[J ] .Free Radic Biol Med, 2017, 112: 141-148. DOI: 10.1016/j.freeradbiomed. 2017.07.020.
LAUNAY N, RUIZ M, GRAU L, et al . Tauroursodeoxycholic bile acid arrests axonal degeneration by inhibiting the unfolded protein response in X-linked adrenol eukodystrophy[J ] . ActaNeuropathol, 2017, 133(2): 283-301. DOI: 10.1007/s00401- 016-1655-9.
RANI S, SREENIVASAIAH P K, KIM J O, et al . Tauroursodeoxycholic acid (TUDCA) attenuates pressure overload-induced cardiac remodeling by reducing endoplasmic reticulum stress[J ] . PLoS One, 2017, 12(4): e0176071. DOI: 10.1371/journal.pone.0176071.
PARIDAENS A, RAEVENS S, COLLE I, et al . Combi-nation of tauroursodeoxycholic acid and N-acetylcysteine exceeds standard treatment for acetaminophen intoxication[J ] .Liver Int, 2017, 37(5): 748-756. DOI: 10.1111/liv.13261.
TAMINIAU A, DRAIME A, TYS J, et al .HOXA1 binds RBCK1/HOIL-1 and TRAF2 and modulates the TNF/NF-κB pathway in a transcription-independent manner[J ] .Nucleic Acids Res, 2016, 44(15): 7331-7349. DOI: 10.1093/ nar/gkw606.
MITSUUCHI Y, BENETATOS C A, DENG Y, et al . Bivalent IAP antagonists, but not monovalent IAP antagonists, inhibit TNF-mediated NF-κB signaling by degrading TRAF2-associated cIAP1 in cancer cells[J ] .Cell Death Discov, 2017, 3: 16046. DOI: 10.1038/cddiscovery.2016.46.
KEESTRA A M, WINTER M G , AUBURGER J J, et al . Manipulation of small Rho GTPases is a pathogen-induced process detected by NOD1[J ] .Nature, 2013, 496(7444): 233- 237. DOI: 10.1038/nature12025.
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