Inflammatory gene regulation describes the complex molecular processes by which the transcription of genes encoding pro-inflammatory and anti-inflammatory mediators is controlled. This critical regulatory mechanism determines the magnitude and duration of the body’s inflammatory response, which is fundamentally linked to chronic disease risk and hormonal signaling dysfunction. Maintaining optimal regulation is essential for systemic health and longevity.
Origin
The term combines inflammatory, referring to the body’s immune response, with gene regulation, the control over gene expression. This concept stems from molecular immunology and endocrinology, recognizing that chronic, low-grade inflammation is a central driver of many age-related and hormonally-sensitive pathologies.
Mechanism
Key transcription factors, such as Nuclear Factor-kappa B (NF-κB), serve as central regulators, becoming activated by inflammatory stimuli like cytokines or metabolic stress. Once activated, NF-κB translocates to the nucleus, binding to DNA sequences to promote the transcription of pro-inflammatory genes, including those for interleukins and tumor necrosis factor-alpha. Conversely, hormones like cortisol and specific dietary compounds can activate anti-inflammatory pathways, effectively dampening this response and restoring immune balance.
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