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Human brown adipose tissue is phenocopied by classical brown adipose tissue in physiologically humanized mice

Authors :
de Jong, Jasper M. A.
Sun, Wenfei
Pires, Nuno D.
Frontini, Andrea
Balaz, Miroslav
Jespersen, Naja Z.
Feizi, Amir
Petrovic, Katarina
Fischer, Alexander W.
Bokhari, Muhammad Hamza
Niemi, Tarja
Nuutila, Pirjo
Cinti, Saverio
Nielsen, Soren
Scheele, Camilla
Virtanen, Kirsi
Cannon, Barbara
Nedergaard, Jan
Wolfrum, Christian
Petrovic, Natasa
de Jong, Jasper M. A.
Sun, Wenfei
Pires, Nuno D.
Frontini, Andrea
Balaz, Miroslav
Jespersen, Naja Z.
Feizi, Amir
Petrovic, Katarina
Fischer, Alexander W.
Bokhari, Muhammad Hamza
Niemi, Tarja
Nuutila, Pirjo
Cinti, Saverio
Nielsen, Soren
Scheele, Camilla
Virtanen, Kirsi
Cannon, Barbara
Nedergaard, Jan
Wolfrum, Christian
Petrovic, Natasa
Publication Year :
2019

Abstract

Human and rodent brown adipose tissues (BAT) appear morphologically and molecularly different. Here we compare human BAT with both classical brown and brite/beige adipose tissues of 'physiologically humanized' mice: middle-aged mice living under conditions approaching human thermal and nutritional conditions, that is, prolonged exposure to thermoneutral temperature (approximately 30 degrees C) and to an energy-rich (high-fat, high-sugar) diet. We find that the morphological, cellular and molecular characteristics (both marker and adipose-selective gene expression) of classical brown fat, but not of brite/beige fat, of these physiologically humanized mice are notably similar to human BAT. We also demonstrate, both in silico and experimentally, that in physiologically humanized mice only classical BAT possesses a high thermogenic potential. These observations suggest that classical rodent BAT is the tissue of choice for translational studies aimed at recruiting human BAT to counteract the development of obesity and its comorbidities.<br />Correction in: Nature Metabolism, vol. 1, issue. 9, page. 927. DOI: 10.1038/s42255-019-0119-7, WOS: 000500745600014QC 20200107

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235100619
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1038.s42255-019-0101-4