Construction method of pancreatic duct epithelial cell and pancreatic acinar cell co-culture system for simulating in vivo microenvironment

A technology of co-culture system and pancreatic duct, applied in the field of cell biology, can solve problems such as damage, pancreatic mucosal barrier damage, and pancreatic juice spillage

Active Publication Date: 2020-01-07
云谱康(大连)生物科技有限公司
View PDF2 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The exocrine part of the pancreas is composed of acini and ducts. Previous AP-related studies have focused on pancreatic acinar cells. Our study believes that the classic retrograde injection of sodium taurocholate into the pancreaticobiliary duct to establish the AP model, the transient high pressure of the pancreatic duct and exogenous...

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Construction method of pancreatic duct epithelial cell and pancreatic acinar cell co-culture system for simulating in vivo microenvironment
  • Construction method of pancreatic duct epithelial cell and pancreatic acinar cell co-culture system for simulating in vivo microenvironment
  • Construction method of pancreatic duct epithelial cell and pancreatic acinar cell co-culture system for simulating in vivo microenvironment

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Specific embodiments of the present invention will be described in detail below in conjunction with specific drawings. It should be noted that the technical features or combinations of technical features described in the following embodiments should not be regarded as isolated, and they can be combined with each other to achieve better technical effects.

[0031] The method for establishing the co-culture system of pancreatic ductal epithelial cells and pancreatic acinar cells of the present invention comprises the following steps:

[0032] Pretreatment of the Transwell cell chamber: Coat the Transwell cell chamber with type I collagen (Product No.: C8062, Beijing Suo Laibao Technology Co., Ltd.) for 18-24 hours, wash with PBS and set aside.

[0033] Extract and isolate primary pancreatic acinar cells from experimental animals; culture HPDE6-C7 human normal pancreatic ductal epithelial cell line; inoculate the resuspended pancreatic acinar cells into the upper layer of ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a construction method of a pancreatic duct epithelial cell and pancreatic acinar cell co-culture system for simulating in vivo microenvironment, and belongs to the technical field of cell biology. The method comprises the steps of inoculating an upper layer of a Transwell dual-layer culturing chamber with original generation pancreatic acinar cells, inoculating a lower layer of the Transwell dual-layer culturing chamber with human pancreatic duct epithelial cells, performing co-culturing, adding sodium taurocholate in the pancreatic duct epithelial cells at the lower layer of the Transwell dual-layer culturing chamber, and observing the vitality, the shape and the apoptosis of the upper layer pancreatic acinar cells. Damage of the pancreatic duct epithelial cells and the pancreatic acinar cells are combined, a non-contact type co-culture manner is adopted for building the pancreatic duct epithelial cell and pancreatic acinar cell co-culture system. In the co-culture system, the two cells can exchange exocytosis secretion substances through Transwell transmembrane. The system can well simulate the pancreatitis induced by cholestasis, and the invention provides an in vitro cell model which can really reflect pancreatitis induced by cholestasis.

Description

technical field [0001] The invention relates to a method for constructing a co-culture system of pancreatic ductal epithelial cells and pancreatic acinar cells simulating the microenvironment in vivo, and belongs to the technical field of cell biology. Background technique [0002] Acute pancreatitis (AP) is a common digestive system disease characterized by pancreatic parenchymal cell injury and inflammatory cascade reaction. The global annual incidence rate of AP is as high as 13-45 / 100,000 people. Among them, about 80% of acute pancreatitis is a mild self-limiting disease with a good prognosis, but about 20-30% of severe acute pancreatitis continues to progress to systemic inflammatory response syndrome or multiple organ failure, resulting in death. The rate is as high as 10-30%. Biliary origin is the main factor in the occurrence of severe acute pancreatitis, biliary tract stones, inflammation, etc. can cause pancreatic duct obstruction, pancreatic mucosal barrier dama...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C12N5/071
CPCC12N5/0676C12N2501/11C12N2501/734C12N2502/22C12N2533/54
Inventor 尚东项红郭方悦陶旭锋
Owner 云谱康(大连)生物科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products