The Morning Journal (Lorain, OH)

Single-cell revolution is underway

New techniques let scientists zero in on individual cells, and the approach is leading to a slew of discoverie­s.

- By Malcolm Ritter

NEW YORK >> Did you hear what happened when Bill Gates walked into a bar? Everybody there immediatel­y became millionair­es — on average.

That joke about a very rich man is an old one among statistici­ans. So why did Peter Smibert use it to explain a revolution in biology?

Because it shows averages can be misleading. And Smibert, of the New York Genome Center, says that includes when scientists are trying to understand the basic unit of life, the cell.

Until recently, trying to study key traits of cells from people and other animals often meant analyzing bulk samples of tissue, producing a mushed-up average of results from many cell types. It was like trying to learn about a banana by studying a strawberry­blueberry- orange-banana smoothie.

In recent years, however, scientists have developed techniques that let them directly study the DNA codes, the activity of genes and other traits of individual cells. The approach has become widely adopted, revealing details about the body that couldn’t be shown before. And it has opened the door to pursuing an audacious goal: listing every cell type in the human body.

“Single- cell analysis is crucial for a comprehens­ive understand­ing of our biology and health,” Dr. Francis Collins, the director of the National Institutes of Health, declared recently. A scientist at the NY Genome Center in New York demonstrat­es equipment used in single-cell RNA analysis on Wednesday. Until recently, trying to study key traits of cells from people and other animals often meant analyzing bulk samples of tissue, producing an average of results from many cell types. But scientists have developed techniques that let them directly study the DNA codes, and its chemical cousin RNA, the activity of genes and other traits of individual cells.

In fact, the journal Science named the techniques that allow singlecell tracking of gene activity over time in developing organisms and organs as its “breakthrou­gh of the year” for 2018. Its announceme­nt declared, “The single-cell revolution is just starting.”

lon, for example, has more than 50 kinds of cells.

It was just five years ago that methods for decoding of DNA and its chemical cousin RNA from individual cells became broadly accessible, according to the journal Nature Methods. New techniques are still being developed to pry more and more secrets out of individual cells.

The single-cell approach is leading to a slew of discoverie­s. In just the past year, for example:

• Scientists closely tracked gene activity within fish and frog embryos, a step toward the longstandi­ng goal of understand­ing how a single fertilized egg can produce an animal. One

study compiled results from more than 92,000 zebrafish embryonic cells.

• Other researcher­s revealed details of the physical connection between pregnant women and the fetus, giving potential clues for understand­ing some causes of stillbirth.

• A study found a pattern of gene activity in some melanoma cells that let them resist immunother­apy, the practice of unleashing the body’s immune system on cancer. That might lead to finding a way to render those cells vulnerable.

And a pair of other studies may affect research into cystic fibrosis, the genetic disease that causes lung infections and limits breathing ability. Scientists have long known that the disease stems from a faulty version of protein called CFTR. The studies identified a type of rare cell in the airway that makes large amounts of CFTR, surpassing earlier but only dimly understood indication­s that such cells existed.

The discovery offers great potential for guiding the developmen­t of new treatments, said Dr. William Skach, senior vice president of research affairs for the Cystic Fibrosis Foundation. Single-cell techniques will be important in studying them further for coming up with new therapies, he said. (Two co-authors of one paper are from the foundation).

At the MDAnderson Cancer Center of the University of Texas, Nicholas Navin uses single-cell DNA studies to reveal different patterns of mutations in various cells of a single tumor. That lets him reconstruc­t when and where those mutations appeared as the tumor evolved from benign cells. And he can identify cells that contain combinatio­ns of muta- Researcher Peter Smibert at the NY Genome Center in New York demonstrat­es a step in single-cell RNA analysis on Wednesday. Until recently, trying to study key traits of cells from people and other animals often meant analyzing bulk samples of tissue, producing an average of results from many cell types. tions that make them the most lethal.

Someday, such research should indicate what treatments to use for particular patients, or which patients have the highest risk of the disease progressin­g, he says. It might also allow doctors to check how well their treatments are working against a cancer over time. A decade or two from now, it might let doctors detect cancers very early by picking up and analyzing the DNA of rare cells in blood tests, he says.

In fact, the journal Science named the techniques that allow singlecell tracking of gene activity over time in developing organisms and organs as its “breakthrou­gh of the year” for 2018.

ganizer Aviv Regev, a biology professor at the Massachuse­tts Institute of Technology and researcher at the Broad Institute of MIT and Harvard. (Her salary is paid by the Howard Hughes Medical Institute, which also supports The Associated Press Health & Science Department.)

The gene map led to identifyin­g thousands of genetic variants that raise or lower the risk of many diseases. But to turn that into therapies, scientists have to know in which cells those variants act, she said. And to run down those cells in the human body, “we have to map all of them.”

Some cells are rarer than others, but these can be just as critical for a functionin­g body as their more plentiful neighbors, she said.

She hopes for a first draft of the cell atlas in about five years, focused on certain organs and tissues of the body. To finish the job might take about a decade, she figures. Regev won’t hazard a guess about how many cell types will be found for the entire human body.

“This is not going to cure all disease immediatel­y,” she said, but “it is a critical stepping stone.”

 ?? MALCOLM RITTER — THE ASSOCIATED PRESS ??
MALCOLM RITTER — THE ASSOCIATED PRESS
 ?? MALCOLM RITTER — THE ASSOCIATED PRESS ??
MALCOLM RITTER — THE ASSOCIATED PRESS

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