A Simple Isolation and Identification Method of Human Placental Myofibroblasts

A technology of fibroblasts and separation method is applied in the field of simple separation and identification of human placental myofibroblastic cells, which can solve the problems of complicated experimental steps, waste of resources and the like, and achieves convenient cell purification, short time-consuming and simple operation. Effect

Active Publication Date: 2017-11-07
BEIJING JING MENG STEM CELL TECH
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, there are few reports on the separation of placental fibroblasts in China at present. Even if there are reports, they mainly focus on the separation of MSCs or stem cells, such as CN 102586184 A (Chinese Patent Application No. 201210044638.6, published on July 18, 2012 ) published an invention entitled "Method for Establishing Placental Mesenchymal Stem Cell Bank"; CN 101395266 A (Chinese Patent Application No. 200680053575.3, date of publication March 25, 2009)
[0006] In the international reports on placental fibroblasts, the isolation methods are all focused on enzyme digestion, but there are many enzymes involved in the digestion process: for example, when Zuzana Strakova of the University of Illinois in the United States isolated placental fibroblasts, collagenase, Deoxyribonuclease, hyaluronidase, and pronase are mixed with four enzymes to digest and obtain fibroblasts. The participation of multiple enzymes will inevitably lead to complex experimental procedures and unnecessary waste of resources.

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
  • A Simple Isolation and Identification Method of Human Placental Myofibroblasts
  • A Simple Isolation and Identification Method of Human Placental Myofibroblasts
  • A Simple Isolation and Identification Method of Human Placental Myofibroblasts

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Embodiment one placental myofibroblasts isolation and culture

[0044] Take fresh placental tissue (within 12 hours) from a normal delivery baby in a sterile biological safety cabinet, use a scalpel to take a tissue about 5 cm long and wide from the center of the placenta, wash it twice with 250 mL of normal saline, and squeeze the placental tissue vigorously. Fully wash out the blood in the tissue, use tweezers and a scalpel to peel off the blood transfusion tissue on the amniotic membrane and decidua basalis; keep the fetal decidua tissue, wash it once with 250mL normal saline, and cut the fetal decidua tissue with a scalpel into a size of 1.5 cm long and 0.5 cm wide; quickly cleaned and disinfected with 75% alcohol for 10 seconds, and then washed twice with 250 mL normal saline; digested with DMEM digestion solution containing 1% collagenase I equal to the volume of tissue fragments at 37 °C After 16-18 h, stop the digestion when there is no placental tissue piece in...

Embodiment 2

[0046] Example 2 Morphological identification of placental myofibroblasts

[0047]Cultivate the myofibroblasts isolated according to the method of Example 1. After 2 days of induction of adherence, scattered spindle-shaped adherent cells can be seen under the microscope. The culture supernatant is completely poured out, and the impurity cells that are not adhered to the wall are removed at the same time, and cultured for 5- After 7 days, radial monoclonal cells can be seen to form, and the monoclonal cells are scraped with a cell scraper and cultured in a 12-well plate until the number of cells reaches 5×10 6 When left or right, it is used for other follow-up identifications.

[0048] It can be seen under the microscope ( figure 1 ) The cells are spindle-shaped or spindle-shaped, have two poles, and are small in size. With the increase of culture time, the cells become larger and grow in fusion. These characteristics are in line with the growth characteristics and morphologic...

Embodiment 3

[0049] Example 3 Identification of surface markers of placental myofibroblasts

[0050] The 3rd passage cells cultured according to Example 1 from different placenta sources were collected respectively, and the cell surface markers were detected by flow cytometry, and the changes of the cell surface markers from different placenta sources were observed. Digest and collect cells, take 1×10 after counting 6 For each cell, wash once with PBS, centrifuge at 1500 rpm for 10 min; discard the supernatant, leave 200 uL, mix the cells by pipetting, add FITC-labeled CD90, CD45, APC-labeled CD29, HLA-DR and PE-labeled CD44 antibodies 10 each μL, and set 1 tube as a blank control, react at 4 °C in the dark for 30 min, wash once with PBS, centrifuge at 1500 rpm for 10 min, discard the supernatant, leave 200 uL, and test on the machine.

[0051] Flow test results figure 2 It shows that the expressions of CD90 (about 99%), CD44 (about 98%), and CD29 (about 97%) in different placental-deri...

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 present invention relates to a method for separating and identifying human placental myofibroblasts. After the placental fetal decidual tissue was mechanically disrupted, it was digested with DMEM digested solution containing collagenase I, and isolated into mononuclear cells. Cultivate under humidity to induce adherence. After 48 hours, change the medium in full to remove non-adherent cells and add fresh medium. After adherent cells form monoclonal cells, each monoclonal cell is cultured separately. When the cells are about 90% confluent, Trypsin passage to obtain myofibroblasts. The invention adopts the combined method of cell morphology, cell cycle, cell surface marker detection, cell adipogenic and osteogenic differentiation ability detection, cell pluripotent stem cell factor detection and cell desmin expression detection to identify the obtained myofibroblasts.

Description

field of invention [0001] The invention relates to a method for isolating myofibroblasts from the decidua surface of human placenta and identifying the myofibroblasts. Background technique [0002] The placenta is considered to be the most attractive "adult stem cell", which can differentiate into muscle cells, liver cells, osteoblasts, chondrocytes, adipocytes and other cells in a suitable in vivo or in vitro environment. Because the source of placental stem cells is relatively convenient, easy to separate and purify, it still has the characteristics of stem cells after multiple passages and expansion, and does not have the characteristics of immune rejection; therefore, it has become a hot spot in stem cell research in recent years. Transplantation, tissue engineering, genetic engineering and other fields have good application prospects. [0003] Myofibroblasts refer to muscle tissue precursor cells containing myofilaments in the cytoplasm, derived from mesoderm stem cell...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C12N5/074C12Q1/68G01N15/14
Inventor 王云虹李志刚丁炜王颖颖高长青杨海莲武晓云黄芳蕾聂晨飞刘洁李大为安志达吴兰兰马瑞吕岩康会彦刘学敏柏小丽
Owner BEIJING JING MENG STEM CELL TECH
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap