bims-mimead Biomed News
on Adipose tissue and metabolic disease
Issue of 2026–05–03
five papers selected by
Rachel M. Handy, University of Guelph



  1. bioRxiv. 2026 Apr 15. pii: 2026.04.09.717542. [Epub ahead of print]
      Bariatric surgery induces profound weight loss and improvement of obesity-associated metabolic dysfunction. Recent studies have shown that adipose tissue undergoes remodeling after weight loss, characterized by a reduction in proinflammatory immune cells, increased vascularization, and a shift in the adipocyte transcriptome, but these studies focused on time points long after surgery. We performed single nucleus RNA-seq (snRNA-seq) in subcutaneous white adipose tissue (SAT) samples from subjects with obesity undergoing bariatric surgery, collected at baseline and at one, six, and twelve months after surgery. We identify profound remodeling of SAT within the first month after surgery, characterized by a surge in lipid-associated macrophages and sharp reductions in specific populations of adipocytes, adipose stromal and progenitor cells (ASPCs), and endothelial cells. Transcriptional profiles strongly suggest that some adipocytes undergo apoptosis soon after surgery, while new adipocytes are generated by de novo differentiation. Mechanistically, the data are consistent with a model whereby coordinated early loss of a hedgehog signaling axis between endothelial cells and an anti-adipogenic population of ASPCs known as adipose regulatory cells (Aregs; ASPC PTCH2 ) enables a transient burst of adipogenesis to occur. Interestingly, very few of these early features seen in human subjects are represented in a mouse model of surgical weight loss.
    DOI:  https://doi.org/10.64898/2026.04.09.717542
  2. Nature. 2026 Apr 29.
      There are increasing numbers of effective drugs to improve obesity-linked metabolic dysfunction; GLP-1R-GIPR co-agonism is effective in the management of obesity and type 2 diabetes1,2, and lanifibranor-a nuclear-acting small-molecule triple agonist of PPARα, PPARγ and PPARδ-is in clinical phase 3 trials for the treatment of metabolic dysfunction-associated steatohepatitis3. Here, seeking to further improve the metabolic efficacy of GLP-1R-GIPR co-agonism, we report the development of a unimolecular quintuple agonist that combines the body weight-reducing and blood glucose-lowering effects of GLP-1R-GIPR co-agonism with the insulin-sensitizing and anti-inflammatory effects of lanifibranor via its targeted delivery into GLP-1R- and GIPR-expressing cells. In vitro, GLP-1-GIP-lanifibranor is indistinguishable from GLP-1-GIP in relation to incretin receptor signalling and shows equal stimulation of insulin secretion in isolated mouse islets. In vivo, however, GLP-1-GIP-lanifibranor outperforms GLP-1R-GIPR co-agonism and semaglutide, further decreasing body weight, food intake and hyperglycaemia in obese and insulin-resistant mice through synergistic incretin and PPAR action. The metabolic action of GLP-1-GIP-lanifibranor is blunted in mice with genetic or pharmacological inhibition of GLP-1R, GIPR or PPARδ and is absent in DIO double incretin receptor-knockout mice, collectively suggesting that GLP-1-GIP-lanifibranor has substantial therapeutic value in the treatment of obesity and diabetes.
    DOI:  https://doi.org/10.1038/s41586-026-10427-5
  3. EMBO Rep. 2026 Apr 27.
      Fasting initiates a coordinated metabolic response to preserve energy balance. As glycogen stores are depleted, the body transitions to mobilizing fatty acids from adipose tissue and generating ketone bodies in the liver to sustain the function of vital organs. A network of hormonal signals and transcriptional programs coordinate these adaptations. Among these, the hepatokine fibroblast growth factor 21 (FGF21) is strongly upregulated during fasting and has been proposed as a key mediator of the fasting response. To investigate the physiological functions of FGF21, we study mice with hepatocyte-specific deletion of Fgf21. Although the liver is the primary source of circulating FGF21 during fasting, its absence in hepatocytes does not alter typical fasting-induced gene expression or key metabolic pathways such as hepatic gluconeogenesis, adipose tissue lipolysis, or ketone production. Instead, we uncover a distinct role for FGF21 in promoting protein appetite following a fast. These findings challenge the conventional view of hepatocyte-produced FGF21 as a fasting-acting hormone and reveal a more specialized function in guiding nutrient selection after energy depletion.
    DOI:  https://doi.org/10.1038/s44319-026-00790-9
  4. JHEP Rep. 2026 Feb 20. pii: S2589-5559(26)00063-7. [Epub ahead of print]8(5): 101792
       BACKGROUND & AIMS: Obesity-associated metabolic dysfunction-associated steatotic liver disease (MASLD) and its progression to steatohepatitis (MASH) with advanced fibrosis pose a major global health challenge. Targeting γ-aminobutyric acid (GABA)ergic system has shown promise in mitigating liver injury. Therefore, we investigated HK3, a positive allosteric modulator of the GABAA receptor, as a potential therapy for MASH, with a particular focus on liver fibrosis and obesity.
    METHODS: Human-derived 3D MASH spheroids (n = 4-27) and hepatic stellate cells (LX2, n = 3-5) were treated with increasing concentrations of HK3 or its derivative HK1 to assess their anti-steatotic, anti-inflammatory and anti-fibrotic efficacy. Molecular and transcriptional responses were assessed by immunoblotting, ELISA, reverse-transcription PCR and RNA sequencing. The in vivo effects of HK3 (10 or 25 mg/kg) were evaluated in carbon tetrachloride-induced fibrosis (n = 10) or diet-induced obesity (n = 6-7) mouse models. Adipocytes (3T3-L1, n = 5-8) and visceral adipose tissue from C57BL/6 mice (n = 6) were treated with HK3 or HK1 to determine their impact on mitochondrial respiratory function by extracellular flux analysis and high-resolution respirometry.
    RESULTS: The most effective concentration of HK3 reduced intracellular lipid content, interleukin secretion and pro-collagen 1αI levels (p <0.0001, p <0.05, p <0.01) in the organotypic 3D human MASH model. In hepatic stellate cells, HK3 and HK1 dose-dependently attenuated TGF-β1-induced fibrotic and inflammatory biomarker expression (p <0.0001) and diminished cell migration (p <0.0001). In vivo, HK3 prevented fibrosis progression (p <0.05) in a carbon tetrachloride mouse model and reduced body fat mass (p <0.0001) in a diet-induced obesity mouse model. Accordingly, HK3 increased proton leakage and mitochondrial uncoupling efficiency in adipocytes (p <0.0001) and visceral adipose tissue (p <0.001).
    CONCLUSION: HK3 attenuates hepatic fibrosis in preclinical MASH models, while reducing body fat through adipocyte mitochondrial uncoupling. Thus, HK3 offers a promising multi-targeted first-in-class pharmacological approach for obesity-associated MASLD.
    IMPACT AND IMPLICATIONS: Obesity-related fatty liver disease can progress to severe liver scarring, yet effective treatments targeting both liver damage and metabolic dysfunction remain rare. This study investigates HK3, a novel small molecule, which reduced liver fat, inflammation, and scarring while also lowering body fat in multiple preclinical models. These findings are particularly relevant for patients with obesity-related fatty liver disease, where current therapies often fail to adequately address fibrosis, the main driver of disease progression. If confirmed in clinical studies, HK3 could support the development of multi-target treatments that simultaneously improve liver health and metabolic balance.
    Keywords:  GABA modulators; Liver fibrosis; TGF-β1 signaling; hepatic stellate cells; metabolic disease; mitochondrial uncoupling; obesity; therapeutics
    DOI:  https://doi.org/10.1016/j.jhepr.2026.101792
  5. Cell Rep. 2026 Apr 29. pii: S2211-1247(26)00379-7. [Epub ahead of print] 117301
      Fecal microbiota transplantation (FMT) has emerged as a promising therapy for gastrointestinal diseases, yet its clinical efficacy remains individually variable. Here, we analyze multi-kingdom and functional profiles in pre- and post-FMT metagenomes from 515 FMTs across 30 cohorts and 12 diseases, in which 94 metagenomes from 44 FMTs are newly collected. We reveal a robust association between clinical efficacy and post-FMT microbiome convergence of recipients toward donors, across diseases. To predict post-FMT microbial convergence, we develop MOZAIC (Microbiome Matching Optimization via Artificial Intelligence), a framework that integrates multi-dimensional donor-recipient microbiota features. MOZAIC achieves an average area under the curve (AUC) of 0.88 and accuracy/recall >0.80 in forecasting microbiome convergence, with 78.7% accuracy in predicting clinical outcomes, and retrospectively simulates a 1.44-fold improvement (from 49.4% to 71.0%) in clinical response rates over baseline. This study establishes microbiome convergence as a key mediator of FMT and provides a scalable tool for precision matching in microbiota-based therapies.
    Keywords:  CP: microbiology; MOZAIC; artificial intelligence; fecal microbiota transplantation
    DOI:  https://doi.org/10.1016/j.celrep.2026.117301