Brain wave: New insight into development
This has been an extremely humbling experience," marvels physiologist Val Galton, Ph.D., a member of the DMS faculty since 1961. She's referring to a recent finding that challenges a piece of conventional wisdom in the field she's worked in for nearly 50 years. Galton began her career by studying thyroid hormone (TH) in the frog—an ideal model for TH studies because of its simplicity; the sole purpose of TH in frog development is to trigger the differentiation that turns tadpoles into frogs. If they lack TH, tadpoles neither grow limbs nor absorb their tails.
Since then, she's developed a longterm collaboration with endocrinologist Donald St. Germain, M.D. They now work with more complex animal models, primarily looking at how TH regulates brain development in mice. "We went from studying shrinking tails to [studying] growing brains," observes St. Germain.
Poor: As a clinician, he has long sought to develop better treatments for hypothyroidism—a TH deficiency in humans. Children who grow up lacking TH develop cretinism, a condition characterized by mental retardation, short stature, and other features of poor development.
There are two thyroid hormones, T4 and
T3; the latter is the active form. It is the job of enzymes called deiodinases to maintain the right ratio of the two. Proper development requires "receiving the right amount of thyroid hormone at the right time," says St. Germain. Recognizing TH's apparent role in brain development, he and Galton began using genetic techniques to wipe out deiodinases in mice, to see the effect of their absence.
Deiodinases are like switches that can be turned on and off to ensure the right balance of T3 and T4 during critical stages of development. The accepted view of TH regulation has been that T3 in
the brain is produced there from T4 by a deiodinase known as type 2 (D2).
For their latest study, published in Endocrinology, Galton and St. Germain used a mouse model lacking D2; such mice are known as D2KO (the "KO" stands for knockout). The results strongly imply that the current view of TH homeostasis in the brain is incomplete. According to that view, D2KO mice should suffer from severe developmental problems. However, they exhibited only relatively mild functional impairment, plus some difficulties hearing and regulating their body temperature. But infants born with an untreated TH deficiency develop cretinism.
Role: So Galton and St. Germain have proposed the existence of important compensatory mechanisms that may minimize functional abnormalities in the absence of D2. "The more we learn about the role of the thyroid hormone in the developing brain, the more optimal a treatment we can offer pregnant mothers and infants suffering from hypothyroidism," explains St. Germain.
Now, armed with mouse models deficient in various combinations of deiodinases, he and Galton are determined to unveil more of the mystery surrounding thyroid hormone regulation during brain development.
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