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  Unraveling the developmental roadmap toward human brown adipose tissue

Carobbio, S., Guenantin, A.-C., Bahri, M., Rodriguez-Fdez, S., Honig, F., Kamzolas, I., et al. (2021). Unraveling the developmental roadmap toward human brown adipose tissue. Stem Cell Reports, 16(3), 641-655. doi:10.1016/j.stemcr.2021.01.013.

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 Creators:
Carobbio, Stefania1, Author
Guenantin, Anne-Claire1, Author
Bahri, Myriam1, Author
Rodriguez-Fdez, Sonia1, Author
Honig, Floris1, Author
Kamzolas, Ioannis1, Author
Samuelson, Isabella1, Author
Long, Kathleen1, Author
Awad, Sherine1, Author
Lukovic, Dunja1, Author
Erceg, Slaven1, Author
Bassett, Andrew1, Author
Mendjan, Sasha1, Author
Vallier, Ludovic1, Author
Rosen, Barry S.1, Author
Chiarugi, Davide2, Author           
Vidal-Puig, Antonio1, Author
Affiliations:
1External Organizations, ou_persistent22              
2Methods and Development Group Computing and Databases Services, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_2205651              

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Free keywords: BAT progenitors; Brown adipose tissue; Development; Differentiation; Human pluripotent stem cells; Thermogenesis
 Abstract: Increasing brown adipose tissue (BAT) mass and activation is a therapeutic strategy to treat obesity and complications. Obese and diabetic patients possess low amounts of BAT, so an efficient way to expand their mass is necessary. There is limited knowledge about how human BAT develops, differentiates, and is optimally activated. Accessing human BAT is challenging, given its low volume and anatomical dispersion. These constraints make detailed BAT-related developmental and functional mechanistic studies in humans virtually impossible. We have developed and characterized functionally and molecularly a new chemically defined protocol for the differentiation of human pluripotent stem cells (hPSCs) into brown adipocytes (BAs) that overcomes current limitations. This protocol recapitulates step by step the physiological developmental path of human BAT. The BAs obtained express BA and thermogenic markers, are insulin sensitive, and responsive to β-adrenergic stimuli. This new protocol is scalable, enabling the study of human BAs at early stages of development.

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Language(s): eng - English
 Dates: 2021-01-212020-07-192021-01-222021-03-09
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1016/j.stemcr.2021.01.013
PMID: 33606988
PMC: PMC7940445
 Degree: -

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Project name : Senior Investigator award
Grant ID : 669879
Funding program : -
Funding organization : European Research Council (ERC)
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Grant ID : -
Funding program : -
Funding organization : Cambridge University Hospital’s National Institute for Health Research Biomedical Research Centre
Project name : -
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Funding program : -
Funding organization : Medical Research Council Cambridge Stem Cell Institute

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Title: Stem Cell Reports
Source Genre: Journal
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Publ. Info: Maryland Heights : Elsevier
Pages: - Volume / Issue: 16 (3) Sequence Number: - Start / End Page: 641 - 655 Identifier: ISSN: 2213-6711
CoNE: https://pure.mpg.de/cone/journals/resource/2213-6711