Home Page  Journal Archive  Members
 Instructions to Authors  Send Article  Join Us
 Contact Us  Site Map
Username
Password
Membership Request
Forget Password
CHAIRMAN MANAGER
Vahidi Serajedin M.D.

EDITOR- IN- CHIEF
Aflatoonian Abbas M.D.

MANAGING EDITOR
Anvari Morteza Ph.D.

EXCUTIVE BOARD
Abdoli Ali Mohammad M.D.
Asadzadeh Kobra B.S.
Khani Parisa M.D.
Mortazavifar Zahrasadat B.S.
Sheikhha Mohammad Hasan M.D. Ph.D.
 
Home Page :: Journal members panel

Journal Title: Autumn 2009
Article title: Isolation and primary culture of ES-like colonies from NMRI mouse embryos

Article PDF File:
Page From: 145 To: 152      

Article abstract:
Background: Embryonic stem (ES) cells are pluripotent cells conventionally isolated from early embryos. Studies have shown that ES cells serve as a practical model for biomedical studies. Objective: The aim of the present study was to optimize culture conditions for establishment of ES-like colonies from NMRI mouse blastocysts as well as 2-cell stage embryos. Materials and Methods: Both expanded blastocysts and 2-cell stage embryos were co-cultured on mouse embryonic fibroblast (MEF). Plating capacity and formation of Inner cell mass (ICM) were examined daily. The differentiation and growth behavior of ICM cells were examined with various procedures. ICMs derived from initially cultured 2-cell or blastocyst embryos were disaggregated either mechanically or enzymatically and seeded onto MEF with or without leukemia inhibitory factor (LIF). The resulted colonies were disaggregated and reseeded onto MEF and the colonies that were morphologically similar to ES cells were evaluated for pluripotency using alkaline phosphatase (ALP) expression as a stem cell marker. Results: No morphologically good ES-like colony was isolated from 2-cell embryos after passages while 273 (79%) good-looking ICMs were isolated from 352 blastocysts. Four sets of colonies remained undifferentiated following passages. Enzymatic method of ICM disaggregation was superior to the mechanical method. Besides all ES-like colonies were obtained from the ICMs cultured in presence of MEF and LIF. Conclusion: Our results show that NMRI mouse ICMs could be isolated and cultured from blastocyst stage embryos with a suitable culture system and ES-like cell colonies remain undifferentiated when cultured with MEF and LIF.

Article KeyWords:
NMRI mouse Inner cell mass Embryonic stem cell.

Article Authors:
Seyed Hassan Eftekhar VaghefiFirst Author
Nehleh Zareii FardOther Author
Zhinoosossadat ShahidzadehOther Author
Seyed Noureddin Nematollahi-mahaniCorresponding Authornnematollahi@kmu.ac.ir

-




Home Page  |   Contact Us  |   Send Article  |   Site Map  

استفاده از مطالب این سایت با ذکر نام سایت مجاز می باشد   -   Copyright © 2007 2009 - Last Update 5-11-2009
Powered By www.itpco.net    www.itpco.ir
( ITPCO ) شرکت توسعه انفورماتیک ایران
تولید کننده سیستم های تخصصی مدیریت نشریات و همایش ها و مورد تائید کمیسیون نظارت بر نشریات پزشکی وزارت بهداشت درمان و آموزش پزشکی کشور