Document Detail

BRITER: a BMP responsive osteoblast reporter cell line.
MedLine Citation:
PMID:  22611465     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: BMP signaling pathway is critical for vertebrate development and tissue homeostasis. High-throughput molecular genetic screening may reveal novel players regulating BMP signaling response while chemical genetic screening of BMP signaling modifiers may have clinical significance. It is therefore important to generate a cell-based tool to execute such screens.
METHODOLOGY/PRINCIPAL FINDINGS: We have established a BMP responsive reporter cell line by stably integrating a BMP responsive dual luciferase reporter construct in the immortalized calvarial osteoblast cells isolated from tamoxifen inducible Bmp2; Bmp4 double conditional knockout mouse strain. This cell line, named BRITER (BMP Responsive Immortalized Reporter cell line), responds robustly, promptly and specifically to exogenously added BMP2 protein. The sensitivity to added BMP may be further increased by depleting the endogenous BMP2 and BMP4 proteins.
CONCLUSION: As the dynamic range of the assay (for BMP responsiveness) is very high for BRITER and as it responds specifically and promptly to exogenously added BMP2 protein, BRITER may be used effectively for chemical or molecular genetic screening for BMP signaling modifiers. Identification of novel molecular players capable of influencing BMP signaling pathway may have clinical significance.
Prem Swaroop Yadav; Paritosh Prashar; Amitabha Bandyopadhyay
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2012-05-14
Journal Detail:
Title:  PloS one     Volume:  7     ISSN:  1932-6203     ISO Abbreviation:  PLoS ONE     Publication Date:  2012  
Date Detail:
Created Date:  2012-05-21     Completed Date:  2012-09-17     Revised Date:  2013-06-24    
Medline Journal Info:
Nlm Unique ID:  101285081     Medline TA:  PLoS One     Country:  United States    
Other Details:
Languages:  eng     Pagination:  e37134     Citation Subset:  IM    
Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, India.
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MeSH Terms
Bone Morphogenetic Proteins / metabolism*,  pharmacology
Cell Line*
Genes, Reporter*
Mice, Knockout
Osteoblasts / metabolism*
Signal Transduction
Reg. No./Substance:
0/Bone Morphogenetic Proteins

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

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