Ben Barres

Near the turn of the 21st century he continued his study of glial cells and the mechanisms behind their ability to generate new neurons.

He studied control of synapses by glia, and the differentiation of astrocytes by endothelial cells.

He investigated the role of the protein Id2 in the control of oligodendrocyte development and established that removing this protein led to premature oligodendrocyte maturation.

Ben A. Barres (September 13, 1954 – December 27, 2017) was an American neurobiologist at Stanford University.

His research focused on the interaction between neurons and glial cells in the nervous system.

Barres was born on September 13, 1954, in West Orange, New Jersey, assigned female as Barbara A. Barres.

As a child, his salesman father and homemaker mother saw him as a tomboy.

He later recalled: "Internally I felt strongly that I was a boy. This was evident in everything about my behavior."

Attending a West Orange school, Barres excelled in mathematics and science and was impressed by his eighth-grade teacher, Jeffrey Davis.

At the age of 17, he learned that he had been born with Müllerian agenesis, for which he received surgical correction.

He obtained a Bachelor of Science in Biology from Massachusetts Institute of Technology (1976), a medical degree (MD) from Dartmouth Medical School (1979), and a residency in neurology at Weill Cornell Medicine.

During his residency, Barres noted the lack of knowledge about the causes or cures of neurodegeneration.

In studying pathology reports, he noticed a correlation between neural degeneration and irregular patterns of glial cells in the brain and, intrigued, resigned his residency to pursue research in neuroscience at Harvard Medical School.

He completed a PhD in neurobiology there in 1990, then did postdoctoral training at University College London under Martin Raff.

In 1993, Barres joined the faculty of Neurobiology at the Stanford School of Medicine.

He transitioned to male in 1997, and became the first openly transgender scientist in the National Academy of Sciences in 2013.

After transitioning to male in 1997, Barres published on sexism in the sciences.

Beginning in 2008, he was chair of the Neurobiology Department at Stanford University School of Medicine.

In 2008, he was appointed to the Chair of Neurobiology at Stanford.

Barres authored or co-authored papers in journals such as Nature Neuroscience, Neuron, Science, and Cell.

His research involved study of mammalian glial cells of the central nervous system (CNS), including the exploration of their function and development.

Much of his early work was published under his deadname.

His first major discovery was how developing neurons provide signals to the myelinating glial cells called the oligodendrocytes that provide insulation on the axons.

Some of his earliest works focussed on vertebrate nervous system development, including how and why many neurons fail to survive shortly after forming connections with their targets.

These studies investigated how this programmed cell death, apoptosis, occurred in such a tremendous scale.

Additionally, he studied processes such as the prerequisites for and consequences of axon myelination, and the interactions of various signaling molecules such as thyroid-hormone and retinoic acid within the formation of glial cells including oligodendrocytes.

Early in his time at Stanford, Barres discovered the importance of glial cells in the formation, development, maturation, and regeneration of neurons.

His lab also discovered and developed methods for the purification and culturing of retinal ganglion cells and the glial cells with which they interact, including the oligodendrocytes and astrocytes of the optic nerve.

In the 2010s Barres's research focused on using techniques such as immunopanning, immunohistochemistry, tissue culturing, and patch clamping to: 1) understand the cell-to-cell interactions in the developmental regulation of nodes of Ranvier and myelin sheaths; 2) determine to what extent glial cells play a role in synapse formation and function of synapses; 3) identify the signals that promote retinal ganglia growth and survival, and how such knowledge of these signals could be regenerated post-trauma; 4) identify the functions and developmental mechanisms of gray matter astrocytes.

In these objectives, his lab discovered a number of novel glial signals for the induction of myelination, axonal sodium channel clustering, and synapse formation processes.

Additionally, his lab characterized these processes and the exact identity of these novel signals.

Barres described experiences of gender discrimination at an early age.

While he was presenting as female prior to transitioning, he was denied at schools from science and mathematics courses, which he liked.

It was a summer science course at Columbia University in New York City that enabled him to pursue further studies in science.

A more serious event happened to his academics in MIT.

After solving a difficult math problem that stumped many male students, his professor charged that it was solved for him by a boyfriend.

He was the top student in the class, but found it hard to get a willing supervisor for research.

He lost a scholarship to a man who had only one publication, while he already had six.

While earning a PhD at Harvard, he was told that he was to win a scientific competition, which was evidently between him and one man; the Dean confided to him, “I have read both applications, and it’s going to be you; your application is so much better.” But the award was given to the male-presenting man, who dropped out of science a year later.

After transitioning, he noticed that people who were not aware of his transgender status treated him with respect much more than when he presented as a woman.