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  • 1
    In: Gene, Elsevier BV, Vol. 636 ( 2017-12), p. 23-29
    Type of Medium: Online Resource
    ISSN: 0378-1119
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 1491012-3
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Lipids Vol. 54, No. 11-12 ( 2019-11), p. 679-686
    In: Lipids, Wiley, Vol. 54, No. 11-12 ( 2019-11), p. 679-686
    Abstract: Visceral obesity is a high‐risk factor for diabetes and metabolic syndrome. Resveratrol, a natural polyphenolic compound, has been reported to inhibit preadipocyte differentiation. However, the effect of resveratrol on human visceral preadipocyte (HPA‐v) differentiation remains largely unknown. LIM domain only 3 ( LMO3 ) promotes human preadipocyte differentiation by enhancing peroxisome proliferator‐activated receptor γ (PPARγ) transcriptional activity, which is the master regulator of adipogenesis. The purpose of our study was to determine the effect of resveratrol (0–50 μM) on HPA‐v proliferation and differentiation, and the role of LMO3 in resveratrol‐mediated regulation of HPA‐v differentiation. Resveratrol inhibited HPA‐v proliferation and differentiation in a dose‐dependent manner, and significantly decreased the mRNA expression levels of PPARG , CCAAT/enhancer‐binding protein α ( CEBPA ), fatty acid‐binding protein 4 ( FABP4 ), acetyl‐CoA carboxylase ( ACC ), and fatty acid synthase ( FAS ) ( p   〈  0.05) at 10, 20, and 50 μM. The mRNA and protein levels of LMO3 were significantly reduced by ≥20 μM resveratrol ( p   〈  0.05), and overexpression of LMO3 partially attenuated resveratrol‐induced reduction of HPA‐v differentiation by enhancing the PPARG transcriptional activity. Together, our study suggested that resveratrol reduced HPA‐v proliferation and differentiation, as well as LMO3, which was partially responsible for the reduction of resveratrol‐mediated adipocyte differentiation.
    Type of Medium: Online Resource
    ISSN: 0024-4201 , 1558-9307
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2030265-4
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2018
    In:  Journal of Animal Science and Biotechnology Vol. 9, No. 1 ( 2018-12)
    In: Journal of Animal Science and Biotechnology, Springer Science and Business Media LLC, Vol. 9, No. 1 ( 2018-12)
    Type of Medium: Online Resource
    ISSN: 2049-1891
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2018
    detail.hit.zdb_id: 2630162-3
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  • 4
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2017
    In:  Scientific Reports Vol. 7, No. 1 ( 2017-03-30)
    In: Scientific Reports, Springer Science and Business Media LLC, Vol. 7, No. 1 ( 2017-03-30)
    Abstract: Intramuscular adipose is conducive to good pork quality, whereas subcutaneous adipose is considered as waste in pig production. So uncovering the regulation differences between these two adiposes is helpful to tissue-specific control of fat deposition. In this study, we found the sensitivity to glucocorticoids (GCs) was lower in intramuscular adipocytes (IMA) compared with subcutaneous adipocytes (SA). Comparison of glucocorticoid receptor (GR) revealed that IMA had lower GR level which contributed to its reduced GCs sensitivity. Higher methylation levels of GR promotor 1-C and 1-H were detected in IMA compared with SA. GR expression decrease was also found in adipocytes when treated with muscle conditioned medium (MCM) in vitro , which resulted in significant inhibition of adipocytes proliferation and differentiation. Since abundant myostatin (MSTN) was detected in MCM by ELISA assay, we further investigated the effect of this myokine on adipocytes. MSTN treatment suppressed adipocytes GR expression, cell proliferation and differentiation, which mimicked the effects of MCM. The methylation levels of GR promotor 1-C and 1-H were also elevated after MSTN treatment. Our study reveals the role of GR in muscle fiber inhibition on intramuscular adipocytes, and identifies myostatin as a muscle-derived modulator for adipose GR level.
    Type of Medium: Online Resource
    ISSN: 2045-2322
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2017
    detail.hit.zdb_id: 2615211-3
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  • 5
    In: Lipids, Wiley, Vol. 52, No. 11 ( 2017-11), p. 939-949
    Abstract: Fat distribution affects economic value in pork production. Intramuscular adipose tissue (IMAT) improves meat quality, whereas subcutaneous adipose tissue (SCAT) is usually regarded as waste. In the present study, we analyzed IMAT/SCAT (I/S) ratios in each pig. Individuals selected from a population of 1200 Suhuai pigs were divided into two cohorts; those with high I/S ratios and those with low I/S ratios, and correlations between nuclear Receptor Co‐activator 3 (NCOA3), a critical gene involved in regulating fat accumulation, and fat distribution were investigated. The ratio of IMAT NCOA3 to SCAT NCOA3 expression levels (NCOA3 I /NCOA3 S ) was higher in the high I/S group compared with the low I/S group. The NCOA3 expression level in fat tissue was positively correlated with fat deposition. miR‐17‐5p was identified as a putative regulator of NCOA3 based on bioinformatics prediction analysis followed by gene expression analysis. The miR‐17‐5p I /miR‐17‐5p S ratio was negatively correlated with the NCOA3 I /NCOA3 S ratio. The predicted relationship between miR‐17‐5p and NCOA3 was further verified by dual luciferase activity assays, qPCR, and western blots. Overexpression of miR‐17‐5p in intramuscular preadipocytes inhibited NCOA3 expression and reduced preadipocyte differentiation. FABP4 and PPARG expression were also significantly decreased, as was triglyceride content. Meanwhile, knockdown of miR‐17‐5p significantly increased NCOA3 expression and promoted intramuscular preadipocyte differentiation. Based on these results, we propose that differential expression of NCOA3 in pig intramuscular and subcutaneous adipose tissue is regulated by miR‐17‐5p.
    Type of Medium: Online Resource
    ISSN: 0024-4201 , 1558-9307
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 2030265-4
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    American Physiological Society ; 2019
    In:  American Journal of Physiology-Endocrinology and Metabolism Vol. 316, No. 4 ( 2019-04-01), p. E635-E645
    In: American Journal of Physiology-Endocrinology and Metabolism, American Physiological Society, Vol. 316, No. 4 ( 2019-04-01), p. E635-E645
    Abstract: The mechanism of adipocyte regulation specifically in muscle and the influence of muscle tissue on intramuscular fat deposition are unknown. Our previous studies have shown that myostatin, a myokine, is involved in inhibiting the differentiation of preadipocytes and may be a potential regulator that affects the deposition of intramuscular fat. Myostatin inhibited adipogenesis by downregulating the expression of glucocorticoid receptor (GR) in porcine preadipocytes. However, the mechanism of regulation is not yet clear. In this study, we demonstrate microRNA (miR-124-3p) mediates regulation of GR by myostatin. We found that miR-124-3p can target GR 3'-UTR and negatively regulate GR expression. We demonstrate that overexpression of miR-124-3p can reduce differentiation of 3T3-L1 cells by inhibiting GR, and vice versa. The expression of miR-124-3p was upregulated in 3T3-L1 cells treated with myostatin. Further study revealed that myostatin also promotes the expression of SMAD4 and its transfer and localization to the nucleus. The activated myostatin/SMAD4 signal promotes the expression of miR-124-3p by SMAD4 binding to the promoter region of miR-124-3p. When myostatin or SMAD4 activity is inhibited, the upregulation of miR-124-3p is also inhibited. All of these findings suggested that myostatin could inhibit adipogenic differentiation of 3T3-L1 cells by activating miR-124-3p to inhibit GR. These data may provide an explanation for how myostatin signaling affects intramuscular fat deposition in a tissue-specific manner.
    Type of Medium: Online Resource
    ISSN: 0193-1849 , 1522-1555
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2019
    detail.hit.zdb_id: 1477331-4
    SSG: 12
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  • 7
    In: Biochemical and Biophysical Research Communications, Elsevier BV, Vol. 472, No. 1 ( 2016-03), p. 68-74
    Type of Medium: Online Resource
    ISSN: 0006-291X
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 1461396-7
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    MDPI AG ; 2017
    In:  International Journal of Molecular Sciences Vol. 18, No. 8 ( 2017-08-20), p. 1799-
    In: International Journal of Molecular Sciences, MDPI AG, Vol. 18, No. 8 ( 2017-08-20), p. 1799-
    Abstract: Due to the paracrine effects of skeletal muscle, the lipid metabolism of porcine intramuscular (i.m.) preadipocytes was different from that of subcutaneous (s.c.) preadipocytes. To investigate the development of i.m. preadipocytes in vivo, the s.c. preadipocytes were cultured with muscle conditional cultured medium (MCM) for approximating extracellular micro-environment of the i.m. preadipocytes. Insulin signaling plays a fundamental role in porcine adipocyte differentiation. The expression levels of insulin receptor (INSR) and insulin-like growth factor 1 receptor (IGF-1R) in i.m. Preadipocytes were higher than that in s.c. preadipocytes. The effects of MCM on adipocyte differentiation, lipid metabolism and insulin signaling transdution were verified. MCM induced the apoptosis of s.c. preadipocytes but not of s.c. adipocytes. Moreover, MCM inhibited adipocyte differentiation at pre-differentiation and early stages of differentiation, while the expression levels of INSR and IGF-1R were increased. Furthermore, MCM treatment increased adipocyte lipolysis and fatty acid oxidation through induction of genes involved in lipolysis, thermogenesis, and fatty acid oxidation in mitochondria. Consistent with the above, treatment of s.c. adipocytes with MCM upregulated mitochondrial biogenesis. Taken together, MCM can approximate the muscle micro-environment and reduce intramuscular adipocyte differentiation and lipid accumulation via regulating insulin signaling.
    Type of Medium: Online Resource
    ISSN: 1422-0067
    Language: English
    Publisher: MDPI AG
    Publication Date: 2017
    detail.hit.zdb_id: 2019364-6
    SSG: 12
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