Human iPSC‐Derived Proinflammatory Macrophages cause Insulin Resistance in an Isogenic White Adipose Tissue Microphysiological System

• Published in: Small (Weinheim an der Bergstrasse, Germany) Germany), 2023-08, Vol.19 (34), p.e2203725-n/a
• Main Authors: Qi, Lin, Matsuo, Koji, Pereira, Ashley, Lee, Yue Tung, Zhong, Fenmiao, He, Yuchen, Zushin, Peter‐James H., Gröger, Marko, Sharma, Aditi, Willenbring, Holger, Hsiao, Edward C., Stahl, Andreas
• Format: Article
• Language: English
• Subjects: Adipose Tissue; Adipose Tissue, White - pathology; Aged; Animals; Body fat; coculture; Humans; human‐induced pluripotent stem cells; Induced Pluripotent Stem Cells; induced pluripotent stem cell‐derived lineages; inflammation; Inflammation - pathology; Insulin; Insulin resistance; Insulin Resistance - physiology; insulin sensitivity; Macrophages; Mice; Mice, Inbred C57BL; Microphysiological Systems; Morphology; Nanotechnology; Obesity; organ‐on‐a‐chip; Palmitic acid; Pathogenesis; Stem cells; white adipose tissues
• ISSN: 1613-6810; 1613-6829; 1613-6829
• DOI: 10.1002/smll.202203725

Chronic white adipose tissue (WAT) inflammation has been recognized as a critical early event in the pathogenesis of obesity‐related disorders. This process is characterized by the increased residency of proinflammatory M1 macrophages in WAT. However, the lack of an isogenic human macrophage‐adipocyte model has limited biological studies and drug discovery efforts, highlighting the need for human stem cell‐based approaches. Here, human induced pluripotent stem cell (iPSC) derived macrophages (iMACs) and adipocytes (iADIPOs) are cocultured in a microphysiological system (MPS). iMACs migrate toward and infiltrate into the 3D iADIPOs cluster to form crown‐like structures (CLSs)‐like morphology around damaged iADIPOs, recreating classic histological features of WAT inflammation seen in obesity. Significantly more CLS‐like morphologies formed in aged and palmitic acid‐treated iMAC‐iADIPO‐MPS, showing the ability to mimic inflammatory severity. Importantly, M1 (proinflammatory) but not M2 (tissue repair) iMACs induced insulin resistance and dysregulated lipolysis in iADIPOs. Both RNAseq and cytokines analyses revealed a reciprocal proinflammatory loop in the interactions of M1 iMACs and iADIPOs. This iMAC‐iADIPO‐MPS thus successfully recreates pathological conditions of chronically inflamed human WAT, opening a door to study the dynamic inflammatory progression and identify clinically relevant therapies. Here, iPSC‐derived macrophages and adipocytes are cocultured in a microphysiological system. Macrophages migrate toward and infiltrate into the 3D adipocytes cluster to form crown‐like structures. M1 but not M2 macrophages induced insulin resistance and dysregulated lipolysis in adipocytes, causing a reciprocal proinflammatory loop. This isogenic system opens a door to study the dynamic inflammatory progression and identify clinically relevant therapies.