Atlas and cell census represent the initial products of the BRAIN Initiative Cell Census Network.
The NIH Brain Research Through Advancing Innovative Neurotechnologies® (BRAIN) Initiative Cell Census Network (BICCN) has unveiled an atlas of cell types and an anatomical neuronal wiring diagram for the mammalian primary motor cortex, derived from detailed studies of mice, monkeys, and humans. This publicly available resource represents the culmination of an international collaborative effort by more than 250 scientists at more than 45 institutions across 3 continents. The atlas provides a foundation for more in-depth study of cell types in the rest of the mammalian brain and may help scientists translate research done in animal models to humans. The findings appear as 17 associated papers published in a dedicated issue of the journal Nature.
“Thanks to this groundbreaking collaboration, we now have a comprehensive understanding of the brain cells found in the motor cortex of the brain and their basic functional properties,” said NIH Director Francis S. Collins, M.D., Ph.D. “The atlas will provide a springboard for future research into the structure and function of the brain within and across species.”
The human brain is an incredibly complex organ, consisting of about one hundred billion neurons and roughly an equivalent number of non-neuronal cells and trillions of neuronal connections. Although all humans share the same general brain structure, a variety of environmental and genetic factors shape how our brains develop and function. In other words, each person’s brain reflects their unique background and life experiences. A full accounting of all the cell types that comprise the brain, their characteristics, and how they differ from individual to individual is crucial for understanding what makes us human.
Importantly, understanding the factors that play a role in the development of the structure and function of the brain is an essential step to learning how diseases — such as schizophrenia, addiction, seizure disorders, and Alzheimer’s disease — develop.
“There is an urgent need to develop therapies for brain-based disorders. Research conducted as part of BICCN will provide scientists with tools that enable precise targeting of cell types and neural networks by genomic therapy for disorders that affect thinking, memory, mood, and movement,” said Walter Koroshetz, M.D., director of the National Institute of Neurological Disorders and Stroke.
Scientific advances in the past 10 years have allowed researchers to move beyond analyzing just the physical characteristics of brain cells to investigating molecular features underlying cell function. Researchers can now examine the transcriptome (the complete set of gene readouts in a cell, which contains instructions for making proteins and other cellular products) and the epigenome of a cell (the set of chemical modifications to the DNA of the cell, which alters the way the cell’s genetic information is expressed). Technical innovations have now scaled to allow for the rapid, cost-effective analysis of tens of millions of individual cells in the effort to better understand the building blocks of the brain.
These scientific advances provide researchers with the opportunity to understand the structure and function of the brain at an unprecedented level of detail. In 2017, the BICCN brought together teams of researchers in a coordinated effort to develop a comprehensive reference of cell types in the human brain, the monkey brain, and the mouse brain. The BICCN researchers set out to catalog and map the different cells of the mammalian brain much like a population census, in which census takers record individuals’ demographic and geographic characteristics. The researchers focused on the primary motor cortex, an area of the brain involved in controlling complex movement that is known to be similar across mammalian species.
In the current series of studies, researchers used a battery of single-cell transcriptome and epigenome measurements obtained from millions of cells in the motor cortex to create a cross-species, data-driven framework of brain cell types. The researchers characterized the brain cell types they found by using a combination of electrophysiological, morphological, and circuit tracing approaches. They also used data from single-cell transcriptome and epigenome analysis to identify unique gene markers that define the many different cell types found in the primary motor cortex. Important to note, this work is more than a compendium of cell types, as it also identifies genetic tools that allow researchers to precisely monitor and modulate the neural activity of specific cell types.
The researchers identified similar cell types across mice, monkeys, and humans but also important differences in gene expression that may be responsible for variations in the way these three species process neural information.
“Through an impressive integration of data from multiple cutting-edge techniques, the BICCN has created a comprehensive reference that catalogs and characterizes the many types of cells found in the mammalian primary motor cortex, describing their proportions, spatial distributions, anatomical and physiological characteristics, and molecular genetic profiles. This work represents a crucial step that will dramatically enhance the pace of advances in understanding the brain,” said Joshua Gordon, M.D., Ph.D., director of the National Institute of Mental Health.
These initial results set the foundation for future research efforts that dive deeper into the structure and function of cells in the mammalian brain. These studies may include efforts to understand how the brain matures and develops, as well as research examining the roles that distinct cell types play in the creation of complex thought and behavior.
“This important work couldn’t have happened without the many minds, institutions, and organizations who came together to solve a very complex problem,” said Andrea Beckel-Mitchener, Ph.D., deputy director of the NIH BRAIN Initiative. “These studies are an example of how collaboration can foster science and set the wheels in motion for future efforts that will revolutionize our ability to study brain function and brain disorders.”
Grants: 1U24MH114827, 1U19MH114831, 1U19MH114821, 1U01MH117072, 1590 1U19MH114830, 1U01MH114829, 1U01MH121282, 1U01MH117023, 1U01MH114825, 1591 1U01MH114819, 1U01MH114812, 1U01MH121260, 1U01MH114824, 1U01MH117079, 1592 1U01MH116990, 1U01MH114828, 1R24MH117295, 5R24MH114793, 5R24MH114788, 1593 5R24MH114815.
The NIH BRAIN Initiative is managed by 10 institutes whose missions and current research portfolios complement the goals of The BRAIN Initiative®: National Center for Complementary and Integrative Health, National Eye Institute, National Institute on Aging, National Institute on Alcohol Abuse and Alcoholism, National Institute of Biomedical Imaging and Bioengineering, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institute on Drug Abuse, National Institute on Deafness and other Communication Disorders, National Institute of Mental Health, and National Institute of Neurological Disorders and Stroke.
About the National Institute of Mental Health (NIMH): The mission of the NIMH is to transform the understanding and treatment of mental illnesses through basic and clinical research, paving the way for prevention, recovery, and cure. For more information, visit the NIMH website.
knowledge to reduce the burden of neurological disease.
About the National Institutes of Health (NIH): NIH, the nation’s medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit www.nih.gov.
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BRAIN Initiative Cell Census Network (BICCN). (2021). A multimodal cell census and atlas of the mammalian primary motor cortex. Nature