Alterations in human gene TRPC5 cause obesity and postpartum depression
Researchers at Baylor College of Medicine, the University of Cambridge and collaborating institutions have discovered that alterations in the human gene TRPC5 cause obesity and postpartum depression.
“Our investigation published in Cell began with the finding that the X chromosomes of two unrelated boys with intense food-seeking behavior, severe obesity and other altered behaviors were missing a small piece that included the TRPC5 gene,” said co-corresponding author Dr. Sadaf Farooqi, professor of metabolism and medicine at the University of Cambridge. “Their mothers had obesity, anxiety and postpartum depression. We found that they were carriers – one of their two X chromosomes also was missing the TRPC5 gene.”
Obesity and postpartum depression are significant global health problems. According to the World Health Organization, obesity has more than doubled in adults since 1990, and quadrupled in adolescents. Postpartum depression occurs in 10 to 15% of mothers and is associated with significant maternal health problems. Globally, postpartum depression remains a major cause of death by suicide in women at a time when maternal mortality due to infections and hemorrhage has declined.
The brain connection
“Previous studies had shown that disrupting gene Trpc5 in the brain causes obesity due to increased food intake and reduced energy expenditure in mice,” said co-corresponding author Dr. Yong Xu, professor of pediatrics – nutrition and associate director for basic sciences at the USDA/ARS Children’s Nutrition Research Center at Baylor College of Medicine.
In the current study, the Xu lab and the Farooqi lab combined the individual expertise of each lab – basic and genetic animal studies in the Xu lab and human genetics and clinical studies in the Farooqi lab – and were able to show that TRPC5 is an important regulator of obesity, postpartum depression and other human behaviors.
To investigate the mechanisms underlying the characteristics observed in people with a defective TRPC5 gene, the researchers generated a mouse model that carries a defective variant of this human gene. Male mice with this mutation gained weight on a high-fat diet and showed anxiety, increased arousal and reduced sociability. Female mice carrying the mutation exhibited depression-like behavior after giving birth and impaired maternal-offspring interactions. Intriguingly, virgin female mice carrying the mutation did not show depression-like behavior.
These studies show that the characteristics and behaviors seen in humans with a defective TRPC5 gene were also present in our mouse model and establish that TRPC5 regulates a spectrum of innate behaviors across mammalian species,” Xu said.
Two types of brain cells are involved
Digging deeper into the mechanisms mediating the actions of this gene, the researchers found that the gene’s actions seem to involve at least two different types of brain cells, Pomc neurons and oxytocin neurons, both in the hypothalamus.
Pomc neurons in the arcuate nucleus of the hypothalamus help regulate body weight by reducing food intake, and about 90% of these cells express Trpc5. The team discovered that genetic disruption of Trpc5 impaired the ability of Pomc neurons to reduce appetite in mice.
The team also discovered high levels of Trpc5 expression in oxytocin neurons in the paraventricular nucleus of the hypothalamus (PVH) in mice. This specific group of neurons in the brain is known to regulate energy balance in the body and the response to stress, emotion and social behaviors including mother-infant bonding.
“Removing the Trpc5 gene from PVH oxytocin neurons in mice caused severe overeating and obesity in both sexes and postpartum depressive behavior and reduced maternal care in females,” Xu said. “On the other hand, overexpressing the functional gene in the neurons of mice carrying a defective gene improved these conditions. Together, the results show that these genetically encoded innate maternal behaviors are mediated by Trpc5 on oxytocin neurons.”
“Our findings not only provide a better understanding of the genetic basis and neural mechanisms involved in obesity and postpartum depression but also have direct clinical implications by advancing the diagnostic practice of these two different human diseases,” Farooqi said.
Our work supports screening for TRPC5 to provide a clinical diagnosis for these conditions.”
In addition, the discovery of the key role TRPC5 plays in these conditions suggests that strategies directed at this protein can potentially lead to new treatments. The authors propose that as overeating and obesity of TRPC5 deficiency is mediated by impaired activation of Pomc neurons, this disorder may be treatable with an MC4R agonist drug licensed for the treatment of genetic obesity syndromes. Oxytocin receptor agonists or gene therapy to restore TRPC5 expression in specific areas of the hypothalamus are potential therapeutic strategies for people with postpartum depression.
Other contributors to this work include Yongxiang Li, Tessa M. Cacciottolo, Na Yin, Yang He, Hesong Liu, Hailan Liu, Yuxue Yang, Elana Henning, Julia M. Keogh, Katherine Lawler, Edson Mendes de Oliveira, Eugene J. Gardner, Katherine A. Kentistou, Panayiotis Laouris, Rebecca Bounds, Ken K. Ong, John R. B. Perry, Inês Barroso, Longlong Tu, Jonathan C. Bean, Meng Yu, Kristine M. Conde, Mengjie Wang, Olivia Ginnard, Xing Fang, Lydia Tong, Junying Han, Tia Darwich, Kevin W. Williams, Yongjie Yang, Chunmei Wang, Shelagh Joss and Helen V. Firth. The authors are affiliated with one or more of the following institutions: Baylor College of Medicine, University of Cambridge, Wellcome-MRC Institute of Metabolic Science, NIHR Cambridge Biomedical Research Center, Exeter Center of Excellence for Diabetes Research, University of Exeter Medical School, University of Texas Southwestern Medical Center at Dallas, Queen Elizabeth University Hospital at Glasgow, Cambridge University Hospitals NHS Foundation Trust and Wellcome Sanger Institute.
This work was supported by a Wellcome Principal Research Fellowship (207462/Z/17/Z), National Institute for Health and Care Research Cambridge Biomedical Research Centre, Botnar Fondation, Bernard Wolfe Health Neuroscience Endowment and an NIHR Senior Investigator Award. Funding for the DECIPHER project was provided by Wellcome. Additional funding was provided by National Institutes of Health grants (T32HD098068, R01 DK119169 and P01 DK119130-03), USDA/ARS (51000-064-01S), American Heart Association Fellowships 20POST35120600, 2020AHA000POST000204188, 23POST1030526 and 23POST1030352, American Diabetes Association Fellowship (1-24-PDF-56), NIHR Clinical Lectureship CL-2019-14-001, Wellcome Transforming Genetic Medicine Initiative grant (WT200990/A/16/Z), Research England “Expanding Excellence in England” award and National Institute for Health and Care Research Exeter Biomedical Research Center and Medical Research Council Unit programs MC_UU_12015/2, MC_UU_00006/2.
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