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Updated: May 12, 2026

An Adipocyte Cell Culture Model to Study the Impact of Protein and Micro-RNA Modulation on Adipocyte Function
Published on: May 4, 2021
Globular adiponectin modulates expression of programmed cell death 4 and miR-21 in RAW 264.7 macrophages through the
Amit Subedi1, Mi Jin Kim, Saroj Nepal
1College of Pharmacy, Yeungnam University, Gyeongsanbuk-do 712-749, Republic of Korea.
Abstract:
MicroRNA-21 and programmed cell death 4 (PDCD4), a downstream target of miR-21, mediate diverse physiological responses. Here we demonstrate that globular adiponectin (gAcrp) modulates expression of miR-21 and PDCD4 in RAW 264.7 macrophages. These effects were abrogated by inhibitors of ERK1/2, JNK or NF-κB. Conditioned media collected from gAcrp-stimulated RAW 264.7 macrophages caused similar effects as direct gAcrp treatment, showing the paracrine effect of gAcrp. These data indicate that gAcrp modulates the miR-21/PDCD4 axis through the ERK and JNK/NF-κB pathways in RAW 264.7 macrophages and further suggest that the miR-21/PDCD4 axis may be a novel target mediating adiponectin-induced biological responses.
Insights
Globular adiponectin (gAcrp) influences microRNA-21 (miR-21) and programmed cell death 4 (PDCD4) levels in macrophages. This modulation occurs via ERK, JNK, and NF-κB pathways, suggesting a new target for adiponectin
Area of Science:
- Cellular and Molecular Biology
- Immunology
- Endocrinology
Background:
- MicroRNA-21 (miR-21) and programmed cell death 4 (PDCD4) are key regulators of cellular processes.
- Adiponectin, an adipokine, plays crucial roles in metabolic and inflammatory responses.
- Understanding the interplay between adiponectin and miR-21/PDCD4 is vital for elucidating cellular signaling.
Purpose of the Study:
- To investigate the effect of globular adiponectin (gAcrp) on miR-21 and PDCD4 expression in RAW 264.7 macrophages.
- To identify the signaling pathways involved in gAcrp-mediated modulation of the miR-21/PDCD4 axis.
- To explore the potential of the miR-21/PDCD4 axis as a mediator of adiponectin's biological effects.
Main Methods:
- Treatment of RAW 264.7 macrophages with globular adiponectin (gAcrp).
- Assessment of miR-21 and PDCD4 expression levels.
- Inhibition of key signaling pathways including ERK1/2, JNK, and NF-κB.
- Analysis of conditioned media from gAcrp-stimulated macrophages to evaluate paracrine effects.
Main Results:
- Globular adiponectin (gAcrp) significantly modulated the expression of miR-21 and PDCD4 in RAW 264.7 macrophages.
- The effects of gAcrp on miR-21 and PDCD4 were dependent on the activation of ERK1/2, JNK, and NF-κB signaling pathways.
- Conditioned media from gAcrp-treated cells mimicked the direct effects of gAcrp, indicating paracrine signaling.
Conclusions:
- Globular adiponectin (gAcrp) regulates the miR-21/PDCD4 axis in macrophages through ERK and JNK/NF-κB signaling pathways.
- The miR-21/PDCD4 axis represents a novel molecular target mediating adiponectin's biological responses.
- These findings provide insights into the molecular mechanisms underlying adiponectin's functions in immune cells.
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