|
FOR IMMEDIATE RELEASE: |
Contact: BD2@gmmb.com |
|
September 26, 2024 |
|
BD² EXPANDS FOUNDATIONAL EFFORT TO UNDERSTAND BIOLOGY OF BIPOLAR DISORDER WITH $36 MILLION IN NEW GRANTS
Grantees include researchers at the University of Oxford, the University of California, Berkeley, Mass General Brigham, and the Broad Institute; BD² opens new round of funding
Washington, D.C. – BD²: Breakthrough Discoveries for thriving with Bipolar Disorder today announced its second installment of Discovery Research grants, totaling nearly $18 million – broadening a comprehensive effort to examine the key mechanisms of bipolar disorder and marking a global expansion of BD². Multidisciplinary teams of scientists and clinicians whose leads are from the University of Oxford, the University of California, Berkeley, Mass General Brigham, and the Broad Institute of MIT and Harvard, will each receive grants of up to $4.5 million over three years, joining current Discovery Research grantees to undertake targeted, innovative research that deepens our understanding of bipolar disorder.
BD² also announced a third round of funding for the program, inviting interested research teams to apply for grants of up to $4.5 million each as well – an additional $18 million in total.
“The Discovery Research program is a cornerstone of BD²’s comprehensive efforts to improve the exploration of causal mechanisms of bipolar disorder,” said Cara Altimus, PhD, managing director for BD² and managing director at the Milken Institute Science Philanthropy Accelerator for Research and Collaboration. “This second round of funding includes projects with direct links to programs throughout BD², building the scientific basis for new diagnostic and treatment approaches.”
The second round of Discovery Research grantees and their areas of focus are as follows:
- Paul Harrison of the University of Oxford will lead his team to investigate the role of voltage-gated calcium channels in bipolar disorder. Using a variety of innovative molecular approaches, the team will determine the function of these proteins in the causes and development of bipolar disorder and assess their potential as drug targets. Throughout, the work will unlock collaboration across BD², especially through the validation of key findings, and has the potential to translate new therapeutic avenues to the BD² Integrated Network.
- Lance Kriegsfeld of the University of California, Berkeley, will lead his team to explore the link between reward-related behavior and disruption in circadian-regulated processes like sleep – and how the interplay may exacerbate manic symptoms in people with bipolar disorder. The project will complement other ongoing work within bipolar-related sleep dysfunction and will help to inform future efforts within the BD² Integrated Network.
- Tracy Young-Pearse of Mass General Brigham will lead her team to examine the role of the immune system in bipolar disorder, identifying how circulating immune cells in the blood can enter the brain and impact its function. Using newly developed organ-chip technology, the team will model how these immune changes affect living human brain cells – ultimately identifying key immune biomarkers and uncovering possibilities for new therapies.
- Jen Pan of the Broad Institute of MIT and Harvard will lead her team to investigate the role of gene-driven dysfunction within key brain structures along the cerebellar thalamic cortical circuit in a model of bipolar disorder to determine if changes in these structures drive disease-associated symptoms. The study will leverage recent genetic findings from the Stanley Center for Psychiatric Research and collaborators, characterize the properties of cerebellar thalamocortical circuits in rodent models, and may generate potential therapeutic opportunities for bipolar patients.
Learn more about the projects and the teams.
The first round of Discovery Research grantees included teams whose leads are from Yale University, Stanford University, New York Genome Center, and the Wyss Institute at Harvard University. That work, comprising research into topics like the genetic risk factors of bipolar disorder and the role of genes in sleep disruption and mania, began last year and is well underway.
BD² also announced the opening of a third round of funding opportunities for the Discovery Research program, inviting scientists across disciplines to learn more about and apply for funding to undertake groundbreaking research into the genetic, molecular, cellular, circuit, and behavioral mechanisms of bipolar disorder.
“Opening the Cycle 3 RFA for the Discovery Research program is a testament to the promise already evident in this approach – and an indicator of our hope and ambition to be able to accelerate scientific progress,” said Eric J. Nestler, MD, PhD, Icahn School of Medicine at Mount Sinai, and Chair, BD² Research Programs. “This program continues to champion innovative thinking and creative strategies from a variety of teams and institutions to better understand bipolar disorder and lift up new opportunities for treatment.”
BD² has dedicated $85 million in funding to research that accelerates scientific understanding of bipolar disorder and advances clinical care through cross-disciplinary collaboration, data sharing, and real-time learning.
###
About BD²: Breakthrough Discoveries for thriving with Bipolar Disorder is the first organization focused on funding and advancing research and care for bipolar disorder on a global scale. Our collaborative, open-science approach is designed to transform and shorten the time it takes for scientific breakthroughs to make a meaningful difference in the lives of the tens of millions of people with bipolar disorder. For more information, please visit bipolardiscoveries.org.
Grantee Quotes
- Paul Harrison of the University of Oxford: “I am excited to lead this innovative multidisciplinary team to explore the role of calcium channels in bipolar disorder. There have long been tantalizing clues about their importance, and the time is right to make significant advances. Our work will investigate how they contribute to the disorder and, particularly, whether and how they can be novel treatment targets. We look forward to joining the BD² community and working together towards achieving this goal.”
- Lance Kriegsfeld of the University of California, Berkeley: “I am delighted to join the BD² community and work with an outstanding team of investigators to examine interactions between the circadian and dopaminergic reward systems in bipolar disorder. Circadian and sleep disturbances, and a heightened response to reward, are key risk factors for the onset and course of bipolar disorder. We look forward to beginning our research examining the mechanistic link between dysregulated circadian timing and reward processing in bipolar disorder to help identify novel treatment targets and therapeutic approaches to care.”
- Tracy Young-Pearse of Mass General Brigham: “I am thrilled to receive this award from BD². This grant will provide us with critical funding to tackle challenging questions regarding the molecular basis neuroimmune interactions in bipolar disorder. Scientists in the Departments of Neurology and Psychiatry here at Mass General Brigham are teaming up for this effort to identify and test novel therapeutic targets for bipolar disorder.”
- Jen Pan of the Broad Institute of MIT and Harvard: “I am honored to lead a team of fantastic colleagues to investigate the role of cerebellar cortical and thalamocortical circuits in bipolar disorder. There have been clues connecting these regions of the brain to bipolar disorder, but recent genetic findings open the door to more deeply understand the underlying mechanisms and potentially uncover new therapeutic opportunities. We are excited to join BD² and are grateful for the support.”