Snapshots of Life: Growing Mini-Brains in a Dish

Brain grown in a lab dish

Credit: Collin Edington and Iris Lee, Department of Biomedical Engineering, MIT

Something pretty incredible happens—both visually and scientifically—when researchers spread neural stem cells onto a gel-like matrix in a lab dish and wait to see what happens. Gradually, the cells differentiate and self-assemble to form cohesive organoids that resemble miniature brains!

In this image of a mini-brain organoid, the center consists of a clump of neuronal bodies (magenta), surrounded by an intricate network of branching extensions (green) through which these cells relay information. Scattered throughout the mini-brain are star-shaped astrocytes (red) that serve as support cells.

Collin Edington and Iris Lee created this striking image in Linda Griffith’s lab at Massachusetts Institute of Technology (MIT), Cambridge. While it looks like a single image, the picture actually took about 12 hours to produce, using a confocal laser scanning microscope to zoom in and capture the microscopic details, pixel by pixel, before digitally stitching the series of images all together. For their painstaking efforts, the team was one of 10 winners in the 2017 Koch Institute Image Awards at MIT, established to recognize and publicly display extraordinary works of art and science.

One of the things that fascinated Edington and Lee about this particular mini-brain was its surprisingly organized structure, which emerged over the course of about two weeks. In fact, one of the most interesting aspects of growing organoids in the lab is that by simply changing the chemical makeup and physical consistency of the hydrogel on which the stem cells are placed, it is possible to influence the ways in which they differentiate and assemble. This enables researchers to tinker with and fine-tune the gel’s characteristics to encourage cells to take on different forms. It also reveals a critical component of the development of complex organs—the cellular environment really matters.

In the experiment captured in this image, the researchers randomly seeded thousands of neural stem cells from human embryonic stem cell lines into a dime-sized well on a standard laboratory plate. Those cells divided and differentiated into hundreds of thousands of cells to form the mini-brain organoid shown above. By studying these mini-brains in the lab, researchers can explore the way a “typical” organoid functions, as well as learn what goes wrong in organoids generated from induced pluripotent stem cells derived from people affected by Alzheimer’s disease or other brain conditions.

Griffith’s lab isn’t stopping with the brain. In fact, this mini-brain is part of a much larger project, funded by NIH and Defense Advanced Research Projects Agency, to produce many different types of “mini-organs”—representing the liver, gut, lung, heart, and more. The goal is to link the individual organoids together to form a “human on a chip.” That integrated approach is important because organs don’t act in isolation in either health or sickness.

Alzheimer’s disease is a good example. While it’s primarily a disease of the brain, it has become increasingly clear that the gut and liver play a role, too. The “human on a chip” platform will make it possible to study such complex interactions in Alzheimer’s disease and many other conditions in the lab, with the ultimate goal to accelerate development of safe and effective new treatments.

Links:

Griffith Lab (MIT, Cambridge, MA)

Human Physiome on a Chip (MIT)

Koch Institute Image Awards (MIT)

Meet Chip (National Center for Advancing Translational Sciences/NIH)

NIH Support: National Center for Advancing Translational Sciences

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s