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Immature adipocyte-derived exosomes inhibit expression of muscle differentiation markers
Koichi Ojima1, Susumu Muroya1, Hiromu Wada2
1Muscle Biology Research Unit, Division of Animal Products Research, National Institute of Livestock and Grassland Science, NARO, Tsukuba, Japan.
Abstract:
Exosomes are released from a variety of cells to communicate with recipient cells. Exosomes contain microRNAs (miRNAs), which are noncoding RNAs that suppress target genes. Our previous proteomic study (FEBS Open Bio 2016, 6, 816-826) demonstrated that 3T3-L1 adipocytes secrete exosome components as well as growth factors, inspiring us to investigate what type of miRNA is involved in adipocyte-secreted exosomes and what functions they carry out in recipient cells. Here, we profiled miRNAs in 3T3-L1 adipocyte-secreted exosomes and revealed suppression of muscle differentiation by adipocyte-derived exosomes. Through our microarray analysis, we detected over 300 exosomal miRNAs during adipocyte differentiation. Exosomal miRNAs present during adipocyte differentiation included not only pro-adipogenic miRNAs but also miRNAs associated with muscular dystrophy. Gene ontology analysis predicted that the target genes of miRNAs are associated primarily with transcriptional regulation. To further investigate whether adipocyte-secreted exosomes regulate the expression levels of genes involved in muscle differentiation, we treated cultured myoblasts with adipocyte-derived exosome fractions. Intriguingly, the expression levels of myogenic regulatory factors, Myog and Myf6, and other muscle differentiation markers, myosin heavy-chain 3 and insulin-like growth factor 2, were significantly downregulated in myoblasts treated with adipocyte-derived exosomes. Immature adipocyte-derived exosomes exhibited a stronger suppressive effect than mature adipocyte-derived exosomes. Our results suggest that adipocytes suppress the expression levels of muscle differentiation-associated genes in myoblasts via adipocyte-secreted exosomes containing miRNAs.
Insights
Adipocyte-secreted exosomes carrying microRNAs suppress muscle cell differentiation. These exosomes downregulate key muscle-specific genes, impacting muscle development and potentially contributing to conditions like muscular dystrophy.
Area of Science:
- Cell biology
- Molecular biology
- Biochemistry
Background:
- Exosomes mediate intercellular communication by transferring molecules like microRNAs (miRNAs).
- 3T3-L1 adipocytes secrete exosomal components and growth factors, suggesting a role in cell signaling.
- MicroRNAs are noncoding RNAs that regulate gene expression by targeting messenger RNAs.
Purpose of the Study:
- To profile microRNAs within exosomes secreted by 3T3-L1 adipocytes.
- To investigate the functional impact of adipocyte-derived exosomes on muscle cell differentiation.
- To identify specific microRNAs involved in the observed effects.
Main Methods:
- Microarray analysis to profile exosomal miRNAs from 3T3-L1 adipocytes.
- Treatment of cultured myoblasts with fractions of adipocyte-derived exosomes.
- Quantitative analysis of muscle differentiation markers and myogenic regulatory factors (e.g., Myog, Myf6).
Main Results:
- Over 300 exosomal miRNAs were detected during adipocyte differentiation.
- Adipocyte-derived exosomes significantly downregulated myogenic regulatory factors (Myog, Myf6) and muscle differentiation markers (myosin heavy-chain 3, IGF2) in myoblasts.
- Immature adipocyte-derived exosomes showed a stronger suppressive effect on muscle differentiation compared to mature ones.
Conclusions:
- Adipocytes secrete exosomes containing miRNAs that actively suppress muscle differentiation.
- The identified exosomal miRNAs target genes involved in transcriptional regulation, impacting muscle development.
- These findings highlight a novel mechanism of intercellular communication influencing muscle health and disease.
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