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从小鼠肝脏中分离并培养原代胆管细胞。

Isolation and Culturing Primary Chaolangiocytes from Mouse Liver.

作者信息

Kudira Ramesh, Sharma Bal Krishan, Mullen Mary, Mohanty Sujit K, Donnelly Bryan, Tiao Gregory M, Miethke Alexander

机构信息

Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

Hematology Department. Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

出版信息

Bio Protoc. 2021 Oct 20;11(20):e4192. doi: 10.21769/BioProtoc.4192.

DOI:10.21769/BioProtoc.4192
PMID:34761065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8554810/
Abstract

Cholangiocytes are epithelial cells lining the intrahepatic and extrahepatic bile ducts. Cholangiocytes perform key physiological functions in the liver. Bile synthesized by hepatocytes is secreted into bile canaliculi, further stored in the gallbladder, and finally discharged into the duodenum. Due to liver injury, biliary epithelial proliferate in response to endogenous or exogenous signals leading to cholangiopathies, inflammation, fibrosis, and cholangiocarcinoma. Cholangiocytes exhibit anatomical and functional heterogeneity, and understanding such diversified functions will potentially help in finding effective therapies for various cholestatic liver diseases. To perform such functional studies, effective cholangiocyte isolation and culture procedures are needed. This protocol will aid in easy isolation and expansion of cholangiocytes from the liver.

摘要

胆管细胞是肝内和肝外胆管内衬的上皮细胞。胆管细胞在肝脏中发挥关键的生理功能。肝细胞合成的胆汁分泌到胆小管中,进一步储存在胆囊中,最终排入十二指肠。由于肝损伤,胆管上皮会对内源性或外源性信号作出增殖反应,导致胆管病、炎症、纤维化和胆管癌。胆管细胞表现出解剖学和功能上的异质性,了解这些多样化的功能可能有助于找到针对各种胆汁淤积性肝病的有效治疗方法。为了进行此类功能研究,需要有效的胆管细胞分离和培养程序。本方案将有助于从肝脏中轻松分离和扩增胆管细胞。

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本文引用的文献

1
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model Organisms.ABCC12 中的有害变异可在特发性慢性胆汁淤积症中被检测到,并导致模型生物中的肝内胆管丢失。
Gastroenterology. 2021 Jul;161(1):287-300.e16. doi: 10.1053/j.gastro.2021.03.026. Epub 2021 Mar 23.
2
Targeting the Gut Microbiome as a Treatment for Primary Sclerosing Cholangitis: A Conceptional Framework.靶向肠道微生物组作为原发性硬化性胆管炎的治疗方法:概念框架。
Am J Gastroenterol. 2020 Jun;115(6):814-822. doi: 10.14309/ajg.0000000000000604.
3
Cholangiocyte pathobiology.胆管细胞病理生物学。
Nat Rev Gastroenterol Hepatol. 2019 May;16(5):269-281. doi: 10.1038/s41575-019-0125-y.
4
Interleukin 2 Promotes Hepatic Regulatory T Cell Responses and Protects From Biliary Fibrosis in Murine Sclerosing Cholangitis.白细胞介素 2 促进肝调节性 T 细胞反应并防止小鼠硬化性胆管炎的胆道纤维化。
Hepatology. 2018 Nov;68(5):1905-1921. doi: 10.1002/hep.30061. Epub 2018 Sep 30.
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Primary sclerosing cholangitis.原发性硬化性胆管炎。
Lancet. 2018 Jun 23;391(10139):2547-2559. doi: 10.1016/S0140-6736(18)30300-3. Epub 2018 Feb 13.
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Role of inflammation and proinflammatory cytokines in cholangiocyte pathophysiology.炎症和促炎细胞因子在胆管细胞病理生理学中的作用。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1270-1278. doi: 10.1016/j.bbadis.2017.07.024. Epub 2017 Jul 25.
7
Biliary bile acids in hepatobiliary injury - What is the link?肝胆损伤中的胆汁酸-它们之间有什么联系?
J Hepatol. 2017 Sep;67(3):619-631. doi: 10.1016/j.jhep.2017.04.026. Epub 2017 Jul 14.
8
Hepatic MDR3 expression impacts lipid homeostasis and susceptibility to inflammatory bile duct obstruction in neonates.肝多药耐药蛋白 3 表达影响新生儿脂质稳态和对炎症性胆管梗阻的易感性。
Pediatr Res. 2017 Jul;82(1):122-132. doi: 10.1038/pr.2017.78. Epub 2017 May 3.
9
Biliary atresia: Where do we stand now?胆道闭锁:我们目前的进展如何?
World J Hepatol. 2016 Dec 28;8(36):1593-1601. doi: 10.4254/wjh.v8.i36.1593.
10
Primary Sclerosing Cholangitis.原发性硬化性胆管炎
N Engl J Med. 2016 Dec 22;375(25):2501-2502. doi: 10.1056/NEJMc1613273.