Have UAB scientists found the genetic key to reverse wrinkles and hair loss associated with aging?

Have UAB scientists found the genetic key to reverse wrinkles and hair loss associated with aging?
In today's society, everyone is interested in staying younger, longer. A research study by UAB scientists is making inroads into how the body ages, with some help from mice, whose cells age similarly to humans. Turning back the hands of time may be possible, UAB's Keshav Singh believes, following studies with mouse models that demonstrate reverse aging of skin and hair is possible. (Getty)

Wrinkled skin and hair loss are hallmarks of aging. What if they could be reversed?

Singh studies the induction of aging within mice cells, with the ability to “turn off” the gene responsible for mitochondrial dysfunction and halting the aging process. (Jeff Hansen/UAB)

Keshav Singh, Ph.D., and colleagues have done just that, in a mouse model developed at the University of Alabama at Birmingham. When a mutation leading to mitochondrial dysfunction is induced, the mouse develops wrinkled skin and extensive, visible hair loss in a matter of weeks. When the mitochondrial function is restored by turning off the gene responsible for mitochondrial dysfunction, the mouse returns to smooth skin and thick fur, indistinguishable from a healthy mouse of the same age.

“To our knowledge, this observation is unprecedented,” said Singh, a professor of genetics in the School of Medicine.

Importantly, the mutation that does this is in a nuclear gene affecting mitochondrial function, the tiny organelles known as the powerhouses of the cells. Numerous mitochondria in cells produce 90 percent of the chemical energy cells need to survive.

In humans, a decline in mitochondrial function is seen during aging, and mitochondrial dysfunction can drive age-related diseases. A depletion of the DNA in mitochondria is also implicated in human mitochondrial diseases, cardiovascular disease, diabetes, age-associated neurological disorders and cancer.

“This mouse model,” Singh said, “should provide an unprecedented opportunity for the development of preventive and therapeutic drug development strategies to augment the mitochondrial functions for the treatment of aging-associated skin and hair pathology and other human diseases in which mitochondrial dysfunction plays a significant role.”

The mutation in the mouse model is induced when the antibiotic doxycycline is added to food or drinking water. This causes depletion of mitochondrial DNA because the enzyme to replicate the DNA becomes inactive.

In four weeks, the mice showed gray hair, reduced hair density, hair loss, slowed movements and lethargy, which are changes reminiscent of natural aging. Wrinkled skin was seen four to eight weeks after induction of the mutation, and females had more severe skin wrinkles than males.

Dramatically, this hair loss and wrinkled skin could be reversed by turning off the mutation. Little change was seen in other organs when the mutation was induced, suggesting an important role for mitochondria in skin compared to other tissues. The wrinkled skin showed changes similar to those seen in both intrinsic and extrinsic aging. Intrinsic aging is the natural process of aging, and extrinsic aging is the effect of external factors, such as wrinkles from excess sun or long-term smoking.

These photos show the hair loss and wrinkled skin after two months of doxycycline induction, and the same mouse a month later, after doxycycline was stopped, allowing restoration of the depleted mitochondrial DNA. (Jeff Hansen/UAB)

Among the details, the skin of induced-mutation mice showed increased numbers of skin cells, abnormal thickening of the outer layer, dysfunctional hair follicles and increased inflammation that appeared to contribute to skin pathology. These are similar to extrinsic aging of the skin in humans. The mice with depleted mitochondrial DNA also showed changed expression of four aging-associated markers in cells, similar to intrinsic aging.

Reversal of the mutation restored mitochondrial function, as well as the skin and hair pathology. This showed that mitochondria are reversible regulators of skin aging and loss of hair, an observation that Singh calls “surprising.”

“It suggests that epigenetic mechanisms underlying mitochondria-to-nucleus cross-talk must play an important role in the restoration of normal skin and hair phenotype,” said Singh, who has a secondary UAB appointment as professor of pathology. “Further experiments are required to determine whether phenotypic changes in other organs can also be reversed to wild-type level by restoration of mitochondrial DNA.”

Co-authors with Singh for the paper, “Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function,” published in the Cell Death and Disease, a Nature online journal, are Bhupendra Singh, Trenton R. Schoeb and Prachi Bajpai, UAB Department of Genetics, and Andrzej Slominski, UAB Department of Dermatology.

This work was supported by Veterans Administration grant 1I01BX001716 and National Institutes of Health grants CA204430, AR071189-01A1 and AR073004.

At UAB, Singh holds the Joy and Bill Harbert Endowed Chair in Cancer Genetics. Slominski holds the Endowed Professorship in Basic Research in the Department of Dermatology.


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