Growth hormone insensitivity and adipose tissue: tissue morphology and transcriptome analyses in pigs and humans

• Published in: Pituitary 2023-12, Vol.26 (6), p.660-674
• Main Authors: Young, Jonathan A., Hinrichs, Arne, Bell, Stephen, Geitgey, Delaney K., Hume-Rivera, Diana, Bounds, Addison, Soneson, Maggie, Laron, Zvi, Yaron-Shaminsky, Danielle, Wolf, Eckhard, List, Edward O., Kopchick, John J., Berryman, Darlene E.
• Format: Article
• Language: English
• Subjects: Adipocytes; Adipose tissue; Adipose Tissue - metabolism; Animal models; Animals; Body fat; Comorbidity; Endocrinology; Gene expression; Gene Expression Profiling; Genotypes; Growth Hormone - metabolism; Growth hormones; Hogs; Human Physiology; Humans; Insulin-Like Growth Factor I - metabolism; Insulin-like growth factors; Medicine; Medicine & Public Health; Obesity; Obesity - genetics; Phenotypes; Receptors, Somatotropin - genetics; Receptors, Somatotropin - metabolism; Swine; Transcriptomes; Transcriptomics
• ISSN: 1386-341X; 1573-7403; 1573-7403
• DOI: 10.1007/s11102-023-01355-y

Purpose Growth hormone receptor knockout ( GHR -KO) pigs have recently been developed, which serve as a large animal model of Laron syndrome (LS). GHR -KO pigs, like individuals with LS, are obese but lack some comorbidities of obesity. The purpose of this study was to examine the histological and transcriptomic phenotype of adipose tissue (AT) in GHR -KO pigs and humans with LS. Methods Intraabdominal (IA) and subcutaneous (SubQ) AT was collected from GHR -KO pigs and examined histologically for adipocyte size and collagen content. RNA was isolated and cDNA sequenced, and the results were analyzed to determine differentially expressed genes that were used for enrichment and pathway analysis in pig samples. For comparison, we also performed limited analyses on human AT collected from a single individual with and without LS. Results GHR -KO pigs have increased adipocyte size, while the LS AT had a trend towards an increase. Transcriptome analysis revealed 55 differentially expressed genes present in both depots of pig GHR -KO AT. Many significant terms in the enrichment analysis of the SubQ depot were associated with metabolism, while in the IA depot, IGF and longevity pathways were negatively enriched. In pathway analysis, multiple expected and novel pathways were significantly affected by genotype, i.e. KO vs. controls. When GH related gene expression was analyzed, SOCS3 and CISH showed species-specific changes. Conclusion AT of GHR -KO pigs has several similarities to that of humans with LS in terms of adipocyte size and gene expression profile that help describe the depot-specific adipose phenotype of both groups.