Hypothalamic ER-associated degradation regulates POMC maturation, feeding, and age-associated obesity

• Published in: The Journal of clinical investigation Vol. 128; no. 3; pp. 1125 - 1140
• Main Authors: Kim, Geun Hyang, Shi, Guojun, Somlo, Diane Rm, Haataja, Leena, Song, Soobin, Long, Qiaoming, Nillni, Eduardo A, Low, Malcolm J, Arvan, Peter, Myers, Jr, Martin G, Qi, Ling
• Format: Journal Article
• Language: English
• Published: United States American Society for Clinical Investigation 01.03.2018
• Subjects: Age; Biomedical research; Care and treatment; Cysteine; Development and progression; Diabetes; Diet; Disease; Endoplasmic reticulum; Energy; Genetic aspects; Health aspects; Homeostasis; Hyperphagia; Hypothalamus; Maturation; Metabolism; Mutation; Neural networks; Neurons; Neuropeptides; Neurosciences; Obesity; Pathogenesis; Phenylalanine; Physiology; Proopiomelanocortin; Proteasomes; Proteins; Quality control; Retention; Rodents; Secretion; Ubiquitination; Protein misfolding; Monogenic diseases; Metabolism; Mouse models; Cell Biology
• ISSN: 0021-9738; 1558-8238
• DOI: 10.1172/jci96420

Pro-opiomelanocortin (POMC) neurons function as key regulators of metabolism and physiology by releasing prohormone-derived neuropeptides with distinct biological activities. However, our understanding of early events in prohormone maturation in the ER remains incomplete. Highlighting the significance of this gap in knowledge, a single POMC cysteine-to-phenylalanine mutation at position 28 (POMC-C28F) is defective for ER processing and causes early onset obesity in a dominant-negative manner in humans through an unclear mechanism. Here, we report a pathologically important role of Sel1L-Hrd1, the protein complex of ER-associated degradation (ERAD), within POMC neurons. Mice with POMC neuron-specific Sel1L deficiency developed age-associated obesity due, at least in part, to the ER retention of POMC that led to hyperphagia. The Sel1L-Hrd1 complex targets a fraction of nascent POMC molecules for ubiquitination and proteasomal degradation, preventing accumulation of misfolded and aggregated POMC, thereby ensuring that another fraction of POMC can undergo normal posttranslational processing and trafficking for secretion. Moreover, we found that the disease-associated POMC-C28F mutant evades ERAD and becomes aggregated due to the presence of a highly reactive unpaired cysteine thiol at position 50. Thus, this study not only identifies ERAD as an important mechanism regulating POMC maturation within the ER, but also provides insights into the pathogenesis of monogenic obesity associated with defective prohormone folding.