Brain cell ‘atlas’ could boost research on neuropsychiatric conditions: Are we there yet?

In a collaborative study led by the University of California San Diego, scientists have examined over 1 million human brain cells to craft intricate maps of gene regulators specific to different brain cell types.

This research not only demonstrates the intricate links between distinct cell categories and prevalent neuropsychiatric disorders but also pioneers the use of artificial intelligence to predict the impact of high-risk gene variations within these cells, potentially unlocking insights into disease development.

This study forms a vital part of the National Institute of Health’s transformative BRAIN Initiative, initiated in 2014, which seeks to revolutionise our understanding of the mammalian brain by advancing innovative neurotechnologies for classifying various neural cell types.

A new study, published in a special edition of Science , highlights the connections between particular cell types and various prevalent neuropsychiatric conditions.

In the human brain, each cell possesses an identical DNA sequence, but various cell types utilise distinct genes in varying quantities.

This diversity results in the creation of numerous brain cell types and adds to the intricacy of neural networks.

Gaining insights into the molecular distinctions among these cell types is crucial for comprehending brain functionality and devising innovative approaches to address neuropsychiatric disorders, such as schizophrenia , bipolar disorder , Alzheimer’s disease , and major depression . Human brain not uniform, an intricate system

The human brain is not uniform in nature. It comprises an incredibly intricate system of neurons and non-neuronal cells, each with distinct roles.

Creating a comprehensive map of these diverse brain cell types and deciphering their collaborative functions will ultimately lead to the identification of novel treatments that can specifically target relevant cell types associated with particular diseases.

Four experts, not involved in this research, spoke to Medical News Today about its findings.

Dr. Ryan S. Sultan is an assistant professor of clinical psychiatry in the Department of Psychiatry at Columbia University Irving Medical Center and the New York State Psychiatric Institute. He noted that the current research “explores an important topic in neuroscience and genetics.”

Dr. Sultan explained that “the study is extensive, encompassing an analysis of chromatin accessibility in 1.1 million cells from various brain regions.”

The researchers pinpointed 107 unique subcategories of brain cells and established connections between aspects of their molecular characteristics and various neuropsychiatric disorders, such as schizophrenia, bipolar disorder, Alzheimer’s disease, and major depression.

Subsequently, the researchers constructed machine learning models aimed at forecasting how specific DNA sequence variations can impact gene regulation and contribute to the development of diseases.

Although these recent findings provide significant insights into the human brain and its disorders, scientists are still in the process of comprehensively mapping the brain.

Dr. James Giordano , the Pellegrino Center professor of neurology and biochemistry at Georgetown University Medical Center, commented on the Science special issue, published on October 13, 2023, which covers research based on The BRAIN Initiative.

He said that “these studies, published in a series of papers in notable medical journals, present the first comprehensive map of molecular mechanisms inherent to specific cell types in discrete areas of the human brain.” “Taken together, these studies, afford a ‘molecular atlas’ of nodes of cells that are genotypically correlated to the expression of certain structural and functional phenotypes that may be involved in a number of neuropsychiatric conditions.”

– Dr. James Giordano Dr. Consuelo Walss-Bass , professor of psychiatry and behavioral sciences and director of the Psychiatric Genetics program at UTHealth Houston, noted that “research of [the] human brain has been historically difficult because of limited ability to obtain human brain samples.”

“However, recently, advances in genomic technologies, coupled with increased availability of postmortem brain tissue, have facilitated the generation of multi-level omics data, including epigenomics, transcriptomics, proteomics, in [the] human brain,” she added. “This is a seminal example of the advances in technology, describing how it is now possible to identify, at the single cell level, DNA regions that are involved in regulating how genes are expressed (genes being ‘turned on or off’). Up till now, there was a lack of technology that allowed for this level of knowledge to be resolved at the individual cell level.”

– Dr. Consuelo Walss-Bass Future is promising, but more research needed

However, Dr. Stefan Ivantu , consultant psychiatrist at ADHD Specialist, said that he felt researchers still had a long way to go until compiling a true “brain cell Atlas.”

“[I]n my opinion,” he told us, “analyzing 1 million cells is considered a small sample given the complexity of the human brain. Very few [people] are aware that the human brain has on average 86 billion cells that are interacting with each other constantly.”

“What makes it even more difficult are the interactions between the cells, which are far more complex,” he added. “However, with more powerful imagistic and AI tool, we may be able to understand the patterns related to specific conditions.”

In Dr. Ivantu’s view, “[a] more promising field is quantum computing, which this linked with the recent AI advances may be more effective in understanding the human brain.”

Nevertheless, he noted that “[i]t is extremely encouraging that researchers are using more technology for the next steps in understanding the human brain, and I believe this is the right approach.”

Dr. Walss-Bass pointed out that the researchers “have identified areas of the genome in individual brain cells that determine whether a gene will become expressed, that is, turned into RNA and then protein, to perform specific functions.”“From this, the authors were then able to correlate genes that had been previously associated with schizophrenia and other psychiatric disorders to areas in the DNA where the expression of these genes is being regulated,” she explained. “Understanding how gene expression is regulated in specific cell types in the brain is a significant advancement that will help to shed light shed light on the neurobiological mechanisms of psychiatric disorders and could lead to development of new therapies to treat these disorders.”– Dr. Consuelo Walss-Bass Dr. Sultan explained that this “research has significant implications for patients and the public.” “It advances our understanding […]

Read more at www.medicalnewstoday.com

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