Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

KIAA1199 (CEMIP) regulates adipogenesis and whole-body energy metabolism

L. Chen, K. Shi, N. Ditzel, W. Qiu, M. Tencerova, LHD. Nielsen, F. Figeac, A. Rauch, Y. Liu, J. Tao, V. Sramkova, L. Rossmeislova, G. Kerckhofs, TN. Parac-Vogt, S. de Bournonville, TL. Andersen, M. Rydén, M. Kassem

. 2025 ; 13 (1) : 43. [pub] 20250402

Jazyk angličtina Země Čína

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc25016190

Grantová podpora
32060155 National Natural Science Foundation of China (National Science Foundation of China)
82260284 National Natural Science Foundation of China (National Science Foundation of China)
NNF15OC0016284 Novo Nordisk Fonden (Novo Nordisk Foundation)
NNF19OC0057449 Novo Nordisk Fonden (Novo Nordisk Foundation)

An increasing number of studies have characterized the bone as an endocrine organ, and that bone secreted factors may not only regulate local bone remodeling, but also other tissues and whole-body metabolic functions. The precise nature of these regulatory factors and their roles at bridging the bone, bone marrow adipose tissue, extramedullary body fat and whole-body energy homeostasis are being explored. In this study, we report that KIAA1199, a secreted factor produced from bone and bone marrow, previously described as an inhibitor of bone formation, also plays a role at promoting adipogenesis. KIAA1199-deficient mice exhibit reduced bone marrow adipose tissue, subcutaneous and visceral fat tissue mass, blood cholesterol, triglycerides, free fatty acids and glycerol, as well as improved insulin sensitivity in skeletal muscle, liver and fat. Moreover, these mice are protected from the detrimental effects of high-fat diet feeding, with decreased obesity, lower blood glucose and glucose tolerance, as well as decreased adipose tissue inflammation, insulin resistance and hepatic steatosis. In human studies, plasma levels of KIAA1199 or its expression levels in adipose tissue are positively correlated with insulin resistance and blood levels of cholesterol, triglycerides, free fatty acids, glycerol, fasting glucose and HOMA-IR. Mechanistically, KIAA1199 mediates its effects on adipogenesis through modulating osteopontin-integrin and AKT / ERK signaling. These findings provide evidence for the role of bone secreted factors on coupling bone, fat and whole-body energy homeostasis.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc25016190
003      
CZ-PrNML
005      
20250731091603.0
007      
ta
008      
250708s2025 cc f 000 0|eng||
009      
AR
024    7_
$a 10.1038/s41413-025-00415-2 $2 doi
035    __
$a (PubMed)40169533
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a cc
100    1_
$a Chen, Li $u Guangxi Key Laboratory of Tumor Immunology and Microenvironment Regulation, Guilin Medical University, Guilin, Guangxi, 541199, China. chenli@glmc.edu.cn $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark. chenli@glmc.edu.cn $1 https://orcid.org/0000000155617612
245    10
$a KIAA1199 (CEMIP) regulates adipogenesis and whole-body energy metabolism / $c L. Chen, K. Shi, N. Ditzel, W. Qiu, M. Tencerova, LHD. Nielsen, F. Figeac, A. Rauch, Y. Liu, J. Tao, V. Sramkova, L. Rossmeislova, G. Kerckhofs, TN. Parac-Vogt, S. de Bournonville, TL. Andersen, M. Rydén, M. Kassem
520    9_
$a An increasing number of studies have characterized the bone as an endocrine organ, and that bone secreted factors may not only regulate local bone remodeling, but also other tissues and whole-body metabolic functions. The precise nature of these regulatory factors and their roles at bridging the bone, bone marrow adipose tissue, extramedullary body fat and whole-body energy homeostasis are being explored. In this study, we report that KIAA1199, a secreted factor produced from bone and bone marrow, previously described as an inhibitor of bone formation, also plays a role at promoting adipogenesis. KIAA1199-deficient mice exhibit reduced bone marrow adipose tissue, subcutaneous and visceral fat tissue mass, blood cholesterol, triglycerides, free fatty acids and glycerol, as well as improved insulin sensitivity in skeletal muscle, liver and fat. Moreover, these mice are protected from the detrimental effects of high-fat diet feeding, with decreased obesity, lower blood glucose and glucose tolerance, as well as decreased adipose tissue inflammation, insulin resistance and hepatic steatosis. In human studies, plasma levels of KIAA1199 or its expression levels in adipose tissue are positively correlated with insulin resistance and blood levels of cholesterol, triglycerides, free fatty acids, glycerol, fasting glucose and HOMA-IR. Mechanistically, KIAA1199 mediates its effects on adipogenesis through modulating osteopontin-integrin and AKT / ERK signaling. These findings provide evidence for the role of bone secreted factors on coupling bone, fat and whole-body energy homeostasis.
650    _2
$a zvířata $7 D000818
650    12
$a adipogeneze $x fyziologie $7 D050156
650    12
$a energetický metabolismus $7 D004734
650    _2
$a myši $7 D051379
650    _2
$a lidé $7 D006801
650    _2
$a inzulinová rezistence $7 D007333
650    _2
$a myši inbrední C57BL $7 D008810
650    _2
$a tuková tkáň $x metabolismus $7 D000273
650    12
$a proteiny $x metabolismus $7 D011506
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a obezita $x metabolismus $7 D009765
650    _2
$a dieta s vysokým obsahem tuků $7 D059305
650    _2
$a hyaluronoglukosaminidasa $7 D006821
655    _2
$a časopisecké články $7 D016428
700    1_
$a Shi, Kaikai $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark
700    1_
$a Ditzel, Nicholas $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark
700    1_
$a Qiu, Weimin $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark
700    1_
$a Tencerova, Michaela $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark $1 https://orcid.org/000000018670425X
700    1_
$a Nielsen, Louise Himmelstrup Dreyer $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark
700    1_
$a Figeac, Florence $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark $1 https://orcid.org/0000000172449438
700    1_
$a Rauch, Alexander $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark $1 https://orcid.org/0000000294297356
700    1_
$a Liu, Yuhang $u Guangxi Key Laboratory of Tumor Immunology and Microenvironment Regulation, Guilin Medical University, Guilin, Guangxi, 541199, China
700    1_
$a Tao, Jiuyuan $u Guangxi Key Laboratory of Tumor Immunology and Microenvironment Regulation, Guilin Medical University, Guilin, Guangxi, 541199, China
700    1_
$a Sramkova, Veronika $u Department of Pathophysiology, Centre for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University, Prague, Czech Republic
700    1_
$a Rossmeislova, Lenka $u Department of Pathophysiology, Centre for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University, Prague, Czech Republic
700    1_
$a Kerckhofs, Greet $u Biomechanics Lab, Institute of Mechanics, Materials, and Civil Engineering, KU Leuven, Leuven, Belgium
700    1_
$a Parac-Vogt, Tatjana N $u Biomechanics Lab, Institute of Mechanics, Materials, and Civil Engineering, KU Leuven, Leuven, Belgium
700    1_
$a de Bournonville, Sébastien $u Biomechanics Section, Department of Mechanical Engineering, KU Leuven, Leuven, Belgium
700    1_
$a Andersen, Thomas Levin $u Institute of Pathology, University of Southern Denmark, Odense, Denmark $1 https://orcid.org/0000000269817276
700    1_
$a Rydén, Mikael $u Department of Medicine (H7), Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden
700    1_
$a Kassem, Moustapha $u Department of Endocrinology and Metabolism, Endocrine Research Laboratory (KMEB), Odense University Hospital & University of Southern Denmark, Odense, Dk-5230, Denmark. mkassem@health.sdu.dk $u Khalifa University, College of Medicine and Health Sciences & Biotechnology Center (BTC), Abu Dhabi, United Arab Emirates. mkassem@health.sdu.dk
773    0_
$w MED00209357 $t Bone research $x 2095-4700 $g Roč. 13, č. 1 (2025), s. 43
856    41
$u https://pubmed.ncbi.nlm.nih.gov/40169533 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20250708 $b ABA008
991    __
$a 20250731091557 $b ABA008
999    __
$a ok $b bmc $g 2366789 $s 1253315
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2025 $b 13 $c 1 $d 43 $e 20250402 $i 2095-4700 $m Bone research $n Bone Res $x MED00209357
GRA    __
$a 32060155 $p National Natural Science Foundation of China (National Science Foundation of China)
GRA    __
$a 82260284 $p National Natural Science Foundation of China (National Science Foundation of China)
GRA    __
$a NNF15OC0016284 $p Novo Nordisk Fonden (Novo Nordisk Foundation)
GRA    __
$a NNF19OC0057449 $p Novo Nordisk Fonden (Novo Nordisk Foundation)
LZP    __
$a Pubmed-20250708

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...