[Cited FineTest ELISA Kit] Current Research on Metabolism and Obesity

FineTest ELISA kit contributes to the research on metabolism and obesity. The immunoassay is designed to measure PDIA3 level in serum.

Article Title: PDIA3 defines a novel subset of adipose macrophages to exacerbate the development of obesity and metabolic disorders
Journal Title: Cell Metabolism
DOI: 10.1016/j.cmet.2024.08.009
IF: 27.7
PMID: 39293433

Abstract: Adipose tissue macrophages (ATMs) play important roles in maintaining adipose tissue homeostasis and orchestrating metabolic inflammation. Given the extensive functional heterogeneity and phenotypic plasticity of ATMs, identification of the authentically pathogenic ATM subpopulation under obese setting is thus necessitated. Herein, we performed single-nucleus RNA sequencing (snRNA-seq) and unraveled a unique maladaptive ATM subpopulation defined as ATF4hiPDIA3hiACSL4hiCCL2hi inflammatory and metabolically activated macrophages (iMAMs), in which PDIA3 is required for the maintenance of their migratory and pro-inflammatory properties. Mechanistically, ATF4 serves as a metabolic stress sensor to transcribe PDIA3, which then imposes a redox control on RhoA activity and strengthens the pro-inflammatory and migratory properties of iMAMs through RhoA-YAP signaling. Administration of Pdia3 small interfering RNA (siRNA)-loaded liposomes effectively repressed adipose inflammation and high-fat diet (HFD)-induced obesity. Together, our data support that strategies aimed at targeting iMAMs by suppressing PDIA3 expression or activity could be a viable approach against obesity and metabolic disorders in clinical settings.

Keywords: adipose tissue macrophages, ATMs, metabolism and obesity, protein disulfide isomerase 3, PDIA3, metabolic stress

Immunoassay

FineTest Product Sample Species Detection Target
Human PDIA3(Protein Disulfide Isomerase A3) ELISA Kit(EH3541) serum human PDIA3

Validated Image

metabolism and obesity

Figure Source: Cell Metab. 2024 Oct 1;36(10):2262-2280.e5. doi: 10.1016/j.cmet.2024.08.009.

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