Summary: A new study reports mast cells play a key role in determining sex differences in the developing brain.
Source: University of Maryland School of Medicine.
Researchers at the University of Maryland School of Medicine (UMSOM) have made a surprising discovery: during fetal development, a particular immune cell seems to play a key role in determining the male or female characteristics of the brain.
“This a totally new discovery,” says Margaret McCarthy, professor and chairman of the UMSOM Department of Pharmacology. “Prior to this, we didn’t know that these cells played a role in this process at all.”
The study, which was published today, appears in the latest issue of the Journal of Neuroscience.
Prof. McCarthy and her colleagues studied immune cells known as mast cells, which originate in the bone marrow but are found on body surfaces such as the skin, mouth, nose and eyes. They are also found on the outside surface of the brain in a membrane known as the meninges. Mast cells are signaling molecules, and when activated, they release a range of molecules, including serotonin, histamine and other inflammatory substances. In general they act as triggers for other immune system cells to respond to an injury or threat to the body.
“Mast cells are basically a signaling system, they release these substances, which signal to other immune cells to come and help out,” says Prof. McCarthy.
At the same time, they also exist, in small numbers, in a specific area of the brain known as the preoptic area. The preoptic area contributes to the control of sexual motivation and parenting behavior, basic behaviors that occur in nearly all species. During development, between 10 and 70 mast cells exist in this area. This study found that in males there are more of the cells in this area than in females, typically about twice as many, and they are more actively releasing their signaling molecules, in particular histamine.
Surprisingly, the histamine released by the mast cells in males signals to another immune cell, the microglia, and instructs them to make prostaglandins, another inflammatory signaling molecule. In previous research, Prof. McCarthy’s lab has shown how prostaglandins induce the development of neural connections in the preoptic area.
In research on rats, Prof. McCarthy and her colleagues found this crucial development occurs in the first week of postnatal development, and plays a large role in determining differences between the male and female brains. She says the findings amazed her: “This one type of cell, and a very small number of these cells, is orchestrating this complex multicellular process to permanently change the circuitry of the brain to make it different in males and females.”
In many animals, including both rats and humans, certain regions of male and female brains are quite different. Imaging studies in humans suggest that females tend to have more cross-hemisphere connections, while males tend to have more connections within each hemisphere.
There are also differences in the size of certain parts of the brain. Certain parts of the hypothalamus are larger in men than women. This divergence may play a role in determining sexual orientation. In gay men, this hypothalamic region is smaller than in heterosexual men; it is typically the same size as in heterosexual women.
On the cellular level male and female brains are also sometimes different. Males tend to have more dense synaptic connections in the preoptic area, while in other areas, females have more dense synaptic connections.
Prof. McCarthy has focused much of her work on the neuroscience of sex differences. In previous research she found sex and gender differences in levels of a protein associated with language acquisition and development. This finding may be associated with higher levels of communication among females in some species.
In previous research, she had found that another kind of immune cell known as microglia appear to play a role in masculinization, in part through their production of prostaglandins, a neurochemical normally associated with illness. In recent years, scientists have increasingly realized that the immune system is integral to the development of the brain;
Prof. McCarthy and her colleagues are now doing additional research on the links between the immune system and brain sex differences. They will next focus on the role of histamine, one of the chemicals released by mast cells, to discover more about precisely what role it plays in the process.
[cbtabs][cbtab title=”MLA”]University of Maryland School of Medicine”Immune Cells Play Key Role in Determining Male or Female Characteristics in Developing Brain.” NeuroscienceNews. NeuroscienceNews, 11 September 2018. <https://neurosciencenews.com/sexual-characteristics-immune-cells-9849/>.[/cbtab][cbtab title=”APA”]University of Maryland School of Medicine(2018, September 11). Immune Cells Play Key Role in Determining Male or Female Characteristics in Developing Brain. NeuroscienceNews. Retrieved September 11, 2018 from https://neurosciencenews.com/sexual-characteristics-immune-cells-9849/[/cbtab][cbtab title=”Chicago”]University of Maryland School of Medicine”Immune Cells Play Key Role in Determining Male or Female Characteristics in Developing Brain.” https://neurosciencenews.com/sexual-characteristics-immune-cells-9849/ (accessed September 11, 2018).[/cbtab][/cbtabs]
Mast Cells in the Developing Brain Determine Adult Sexual Behavior
Many sex differences in brain and behavior are programmed during development by gonadal hormones, but the cellular mechanisms are incompletely understood. We found that immune system-derived mast cells are a primary target for the masculinizing hormone, estradiol, and that mast cells are in turn primary mediators of brain sexual differentiation. Newborn male rats had greater numbers and more activated mast cells in the preoptic area (POA), a brain region essential for male copulatory behavior, than female littermates during the critical period for sexual differentiation. Inhibiting mast cells with a stabilizing agent blunted the masculinization of both POA neuronal and microglial morphology and adult sex behavior, while activating mast cells in females, even though fewer in number, induced masculinization. Treatment of newborn females with a masculinizing dose of estradiol increased mast cell number and induced mast cells to release histamine, which then stimulated microglia to release prostaglandins and thereby induced male-typical synaptic patterning. These findings identify a novel non-neuronal origin of brain sex differences and resulting motivated behaviors.
We found that immune system-derived mast cells are a primary target for the masculinizing hormone, estradiol, and that mast cells are in turn primary mediators of brain sexual differentiation. These findings identify a novel non-neuronal origin of brain sex differences and resulting motivated behaviors.