• Preventive Nutrition and Food Science
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• 제21권1호
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• pp.62-67
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• 2016

Green tea (Camellia sinensis) is one of the most popular beverages in the world and has been acknowledged for centuries as having significant health benefits. (-)-Epigallocatechin-3-gallate (EGCG) is the most abundant catechin in green tea, and it has been reported to have health benefit effects. Peroxisome proliferator-activated receptor ${\gamma}$ coactivator $(PGC)-1{\alpha}$ is a crucial regulator of mitochondrial biogenesis and hepatic gluconeogenesis. The objective of this study was to investigate whether EGCG from green tea can affect the ability of transcriptional regulation on $PGC-1{\alpha}$ mRNA expression in HepG2 cells and 3T3-L1 adipocytes. To study the molecular mechanism that allows EGCG to control $PGC-1{\alpha}$ expression, the promoter activity levels of $PGC-1{\alpha}$ were examined. The $PGC-1{\alpha}$ mRNA level was measured using quantitative real-time PCR. The -970/+412 bp of $PGC-1{\alpha}$ promoter was subcloned into the pGL3-Basic vector that includes luciferase as a reporter gene. EGCG was found to up-regulate the $PGC-1{\alpha}$ mRNA levels significantly with $10{\mu}mol/L$ of EGCG in HepG2 cells and differentiated 3T3-L1 adipocytes. $PGC-1{\alpha}$ promoter activity was also increased by treatment with $10{\mu}mol/L$ of EGCG in both cells. These results suggest that EGCG may induce $PGC-1{\alpha}$ gene expression, potentially through promoter activation.

• Preventive Nutrition and Food Science
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• 제21권4호
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• pp.317-322
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• 2016

Mitochondrial biogenesis is a complex process requiring coordinated expression of nuclear and mitochondrial genomes. The peroxisome proliferator-activated receptor gamma co-activator 1-alpha (PGC-$1{\alpha}$) is a key regulator of mitochondrial biogenesis, and it controls mitochondrial DNA (mtDNA) replication within diverse tissues, including muscle tissue. The aim of this study was to investigate the effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on mtDNA copy number and PGC-$1{\alpha}$ promoter activity in $C_2C_{12}$ muscle cells. mtDNA copy number and mRNA levels of genes related to mitochondrial biogenesis such as PGC-$1{\alpha}$, nuclear respiratory factor 1 (NRF1) and mitochondrial transcription factor A (Tfam) were assayed by quantitative real-time PCR. The PGC-$1{\alpha}$ promoter from -970 to +412 bp was subcloned into the pGL3-basic vector, which includes a luciferase reporter gene. Both EPA and DHA significantly increased mtDNA copy number, dose and time dependently, and up-regulated mRNA levels of PGC-$1{\alpha}$, NRF1, and Tfam. Furthermore, EPA and DHA stimulated PGC-$1{\alpha}$ promoter activity in a dose-dependent manner. These results suggest that EPA and DHA may modulate mitochondrial biogenesis, which was partially associated with increased mtDNA replication and PGC-$1{\alpha}$ gene expression in $C_2C_{12}$ muscle cells.

• 대한의생명과학회지
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• 제18권2호
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• pp.139-145
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• 2012

RFLP of PGC-$1{\alpha}$ gene of 285 Korean women was analyzed by PCR and HpaII restriction. We evaluated the correlation between PGC 1 genotypes and biochemical results, using the results of RFLP. Study subjects were divided into 3 groups: normal group (who has been average value of serum biochemical analysis), upper group (who has been higher value than average value), and low group (who have been lower value than average value). The frequencies of $H_1H_1$, $H_1H_2$, and $H_2H_2$ genotypes were 92 (32%), 85 (32%), and 108 (38%) respectively, and the ratio between $H_1$ and $H_2$ alleles was 1:1.1. There were no meaningful differences between biochemical results and PGC-$1{\alpha}$ genotypes in the normal group. But, in upper group, there was significant difference in total cholesterol (P=0.04) level. In the result of Turkey multiple comparison test, the P value of $H_1H_1$ and $H_2H_2$ was 0.059. In upper group, there were noticeable differences also in triglyceride (P=0.034) level and glucose (P=0.043) level, respectively. There were important differences between $H_1H_1$ type and $H_1H_2$ type in triglyceride (P=0.029) level and between $H_1H_2$ type and $H_2H_2$ type in glucose (P=0.040) level. This study may provide the PGC-$1{\alpha}$ genotype patterns for the amounts of lipid and glucose in the serum. $H_2$ allele (Ser482) of PGC-$1{\alpha}$ gene may be related with upper group in Korean women.

• Molecules and Cells
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• 제39권2호
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• pp.87-95
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• 2016

Sirt1 is the most prominent and extensively studied member of sirtuins, the family of mammalian class III histone deacetylases heavily implicated in health span and longevity. Although primarily a nuclear protein, Sirt1's deacetylation of Peroxisome proliferator-activated receptor Gamma Coactivator-$1{\alpha}$ (PGC-$1{\alpha}$) has been extensively implicated in metabolic control and mitochondrial biogenesis, which was proposed to partially underlie Sirt1's role in caloric restriction and impacts on longevity. The notion of Sirt1's regulation of PGC-$1{\alpha}$ activity and its role in mitochondrial biogenesis has, however, been controversial. Interestingly, Sirt1 also appears to be important for the turnover of defective mitochondria by mitophagy. I discuss here evidences for Sirt1's regulation of mitochondrial biogenesis and turnover, in relation to PGC-$1{\alpha}$ deacetylation and various aspects of cellular physiology and disease.

• 생명과학회지
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• 제28권7호
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• pp.857-863
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• 2018

본 연구는 함초의 보충식이가 고지방식이 흰쥐의 혈청 및 조직의 중성지방 농도와 골격근 내 $PGC-1{\alpha}$와 $PPAR-{\gamma}$ 단백질 발현에 미치는 영향에 대하여 연구하였다. SD계 수컷 흰쥐를 대조군(CD, n=8), 고지방식이군(HD, n=8), 고지방식이+ 5% 함초 보충식이군(SD, n=8)으로 분류하여 8주간 사육하였다. 그 결과 SD군의 지방조직 중량은 HD군에 비해 약 25%정도 유의하게 감소한 반면 골격근의 중량은 SD군이 HD군에 비해 약 5%정도 유의하게 증가하였다(p<0.01). SD군의 혈청과 간장 내 중성지방은 HD군에 비해 약 20% 유의하게 감소하였다(p<0.05). SD군의 골격근 내 $PGC-1{\alpha}$ 와 $PPAR-{\gamma}$ 단백질 발현은 HD군에 비해 1.5배 유의하게 높게 나타났다(p<0.01). 이상의 결과로 부터 함초 보충은 골격근 내 $PGC-1{\alpha}$와 $PPAR-{\gamma}$ 단백질 발현의 증가를 통하여 지방감소 및 근육량 증가에 효과적이었음이 시사되었다.

• 생명과학회지
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• 제24권1호
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• pp.67-73
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• 2014

본 연구는 안정 시 고지방식이 흰쥐의 골격근에서 PPAR-${\delta}$, PPAR-${\gamma}$ 그리고 PGC-$1{\alpha}$ 단백질 발현에 손바닥선인장 보충이 미치는 효과에 대하여 연구하였다. SD계 수컷 흰쥐 16마리를 무작위로 대조군(CG, n=8)과 실험군(EG, n=8)으로 분류하였다. 8주 동안 대조군은 고지방식이를 부하하였으며, 실험군은 5% 손바닥선인장을 보충식이하였다. 본 실험결과, 복부지방과 고환부 지방 중량은 EG군이 CG군에 비해 유의하게 낮게 나타났다(p<0.01). 또한 혈당, 중성지방, 총콜레스테롤의 농도도 EG군이 CG군에 비해 유의하게 낮게 나타났다(p<0.01). 한편, 골격근에서 PPAR-${\gamma}$와 PGC-$1{\alpha}$ 단백질 발현은 EG군이 CG군에 비해 유의하게 높게 나타났다(p<0.05). 이상의 결과로부터 손바닥선인장 보충이 고지방식이 흰쥐의 혈당과 중성지방 농도의 감소와 골격근에서 PPAR-${\gamma}$와 PGC-$1{\alpha}$ 단백질 발현을 증가시킴으로서 체지방을 감소시켜 체중증가 억제에 긍정적인 영향을 미치는 것으로 나타났다.

• Biomolecules & Therapeutics
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• 제28권3호
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• pp.240-249
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• 2020

Despite the therapeutic effect of mesenchymal stem cells (MSCs) in ischemic diseases, pathophysiological conditions, including hypoxia, limited nutrient availability, and oxidative stress restrict their potential. To address this issue, we investigated the effect of melatonin on the bioactivities of MSCs. Treatment of MSCs with melatonin increased the expression of peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α). Melatonin treatment enhanced mitochondrial oxidative phosphorylation in MSCs in a PGC-1α-dependent manner. Melatonin-mediated PGC-1α expression enhanced the proliferative potential of MSCs through regulation of cell cycle-associated protein activity. In addition, melatonin promoted the angiogenic ability of MSCs, including migration and invasion abilities and secretion of angiogenic cytokines by increasing PGC-1α expression. In a murine hindlimb ischemia model, the survival of transplanted melatonin-treated MSCs was significantly increased in the ischemic tissues, resulting in improvement of functional recovery, such as blood perfusion, limb salvage, neovascularization, and protection against necrosis and fibrosis. These findings indicate that the therapeutic effect of melatonin-treated MSCs in ischemic diseases is mediated via regulation of PGC-1α level. This study suggests that melatonin-induced PGC-1α might serve as a novel target for MSC-based therapy of ischemic diseases, and melatonin-treated MSCs could be used as an effective cell-based therapeutic option for patients with ischemic diseases.

• 한국식품영양과학회지
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• 제43권7호
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• pp.963-971
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• 2014

본 연구에서는 4주간의 고지방식이와 지구성 운동이 골격근의 PGC-$1{\alpha}$, PPAR-${\gamma}$ 및 인슐린 저항성(glucose uptake, GLUT-4)에 미치는 영향을 분석하였다. 인슐린 민감도 지표인 혈당내성검사에서는 일반식이와 비교하여 고지방식이에서 포도당 투여 후 30분과 60분에서 유의하게 증가하였으며, 운동집단에서는 일반식이와 고지방식이집단에 비해 유의하게 감소한 것을 알 수 있었다. 골격근의 포도당 운반률, PGC-$1{\alpha}$, GLUT-4, PPAR-${\gamma}$의 결과에서는 일반식이에 비해 고지방식이집단에서 감소하는 경향이 나타났으나 통계적으로 유의한 차이가 없는 것으로 나타났다. 그러나 운동집단(저/중/고강도운동)에서는 일반/고지방식이집단과 비교하여 유의하게 증가한 것으로 나타났다. 운동집단의 운동강도 차이에서 GLUT-4와 PPAR-${\gamma}$는 집단 간 유의한 차이가 없는 것으로 나타났다. 그러나 골격근의 포도당 운반률과 PGC-$1{\alpha}$ 단백질 발현은 저/중강도 운동과 비교하여 고강도 운동이 유의하게 증가한 것을 알 수 있었다. 이상의 결과를 종합해 볼 때 4주간의 고지방식이는 whole body의 인슐린 저항성을 발생시켰으나 근육 내 인슐린 저항에는 영향을 미치는 못한 것으로 사료된다. 그러므로 추후 고지방식이의 함량, 섭취 기간 등을 고려한 연구가 필요할 것으로 생각된다. 또한 4주간의 지속적인 지구성 운동이 고지방식이로 인해 발생된 골격근 인슐린 저항성을 감소시키는데 효과적인으로 나타났으나 운동 강도에 따른 골격근의 포도당 운반률, PGC-$1{\alpha}$, GLUT-4, PPAR-${\gamma}$의 변화가 인슐린 저항성이 개선시켰다고 설명하기는 부족한 것으로 판단된다. 그러므로 추후 본 연구의 결과를 바탕으로 운동 형태(운동 기간, 운동강도)에 따른 골격근의 PGC-$1{\alpha}$와 insulin signalling pathway에 대한 세부적인 연구가 필요할 것으로 생각된다.

• 한국체육학회지인문사회과학편
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• 제55권4호
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• pp.507-516
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• 2016

본 연구는 지구성 운동 후 안정시 PGC-1α mRNA와 단백질의 안정성이 PPARβ/δ의 영향을 받는지 확인하는 것이다. 전기 자극 유전자 전이법(electroporation; EPO)을 이용하여 PPARβ/δ와 empty vector(EV) 유전자를 각각 생쥐의 왼쪽과 오른쪽 tibialis anterior(TA)근육에 전이하였으며, 처치하지 않은 대조군(control)과 1회 지구성 운동 후 시간에 경과에 따른 mRNA와 단백질을 비교하였다. 생쥐는 5시간 수영 운동을 1회 실시하였으며, 운동 직후(0h), 24시간(24h) 및 54시간(h)이 경과한 후 TA근육을 적출하였다. 운동 직후(0h) 대조군, EV 및 PPARβ/δ가 과발현된 근육의 PGC-1α mRNA는 좌업 그룹보다 각각 6.8배(p<.001)배, 6.2배(p<.001) 및 7.1배(p<.001) 증가하였으나, 24h 및 54h에 좌업 그룹수준으로 회복되었다. 운동 후 24h에 EV가 처치된 근육은 PGC-1α 및 PGC-1α ubiquitination이 좌업 그룹보다 각각 2.2배 및 1.74배 증가하였으나, 운동 후 54h에 좌업 그룹수준으로 회복되었다. PPARβ/δ 처치 그룹의 PGC-1α는 운동 후 24h와 54h에 좌업 그룹보다 각각 2.5배와 2.2배 증가하였으나 PGC-1α ubiquitination은 증가하지 않았다. 따라서 PPARβ/δ 과발현은 지구성 운동에 의한 PGC-1α mRNA 단백질 안정성에 영향을 미치지 않는다. 그러나 PPARβ/δ 과발현은 지구성 운동으로 증가된 PGC-1α mRNA가 단백질로 전환된 후 PGC-1α의 안정성을 증가시킨다.

• 한국식품영양학회지
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• 제30권5호
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• pp.900-907
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• 2017

This study was performed to investigate the body fat-lowering effect of garlic powder in peroxisome proliferator-activated receptor ${\gamma}$ coactivator-$1{\alpha}$(PGC-$1{\alpha}$)-luciferase transgenic mice (TG). In this study, we generated transgenic mice with a PGC-$1{\alpha}$ promoter (-970/+412 bp) containing luciferase as a reporter gene. Mice were fed a 45% high-fat diet for 8 weeks to induce obesity. Subsequently, mice were maintained on either a high-fat control diet (CON), or high-fat diets supplemented with 2% (GP2) or 5% (GP5) garlic powder for an additional 8 weeks. Dietary garlic powder reduced the body weight in the GP2 and GP5 groups, compared to the CON group. Furthermore, garlic supplementation significantly decreased the plasma levels of triglycerides, total cholesterol, and leptin in the GP5 group, compared to the CON group. Specifically, luciferase activity in liver, white adipose tissue (WAT), and brown adipose tissue (BAT) was increased by garlic supplementation in a dose-dependent manner. These results suggest that the body fat-lowering effect of garlic powder might be related to PGC-$1{\alpha}$ by the increase in luciferase activity in liver, WAT, and BAT. Furthermore, transgenic mice might be useful for evaluating the body fat-lowering effect of various health functional foods.