Stem Cells Help Lizard Regenerate a Perfect Tail for First Time in More Than 250 Million Years

Mourning Gecko

A lizard species known as a mourning gecko can regenerate its tail, but the replacement is an imperfect copy of the original. Credit: USC/Lozito Lab

USC researchers’ experiment helps inform efforts to improve wound-healing in humans.

Lizards can regrow severed tails, making them the closest relative to humans that can regenerate a lost appendage. But in lieu of the original tail that includes a spinal column and nerves, the replacement structure is an imperfect cartilage tube. Now, for the first time, a USC-led study in Nature Communications describes how stem cells can help lizards regenerate better tails.

“This is one of the only cases where the regeneration of an appendage has been significantly improved through stem cell-based therapy in any reptile, bird or mammal, and it informs efforts to improve wound healing in humans,” said the study’s corresponding author Thomas Lozito, an assistant professor of orthopedic surgery and stem cell biology and regenerative medicine at the Keck School of Medicine of USC.

These new and improved lizard tails exhibit what is known as “dorsoventral patterning”—meaning they have skeletal and nerve tissue on the upper or dorsal side, and cartilage tissue on the lower or ventral side.

“Lizards have been around for more than 250 million years, and in all that time no lizard has ever regrown a tail with dorsoventral patterning, until now,” said Lozito. “My lab has created the first regenerated lizard tails with patterned skeletons.”

To achieve this, the team of scientists from the medical schools at USC and the University of Pittsburgh analyzed how lizard tails form during adult regeneration, compared to embryonic development. In both cases, neural stem cells or NSCs—the stem cells that build the nervous system—play a central role.

Adult NSCs produce a molecular signal that blocks skeletal and nerve formation and encourages cartilage growth, effectively “ventralizing” both sides of the tail. This results in the cartilage tube typical of regenerated tails.

New Lizard Tail

Histology of a fully regenerated mourning gecko tail. Muscle is colored in white, cartilage in red, proliferating cells in green, and cell nuclei in blue. Credit: USC/Lozito Lab

Even in the absence of this ventralizing signal, adult NSCs are incapable of generating new nerve tissue for the dorsal side of the tail.

In contrast, embryonic NSCs produce this “ventralizing” signal only in the cartilage region that becomes the lower or ventral side of the tail. Meanwhile, in the absence of this signal, the upper or dorsal side develops skeletal and nerve tissue. Thus, the tail acquires the intricate dorsoventral patterning characteristic of original embryonic appendages.

However, if embryonic NSCs are implanted into adult tail stumps, they respond to the ventralizing signal, and fail to develop into dorsal structures.

To overcome these obstacles, Lozito’s team used gene-editing tools to make embryonic NSCs unresponsive to the ventralizing signal, and surgically implanted these cells into adult tail stumps—leading to the regeneration of perfect tails.

Histology of Mourning Gecko Blastema

Histology of mourning gecko blastema. Muscle is colored in white, cartilage in red, proliferating cells in green, and cell nuclei in blue. Credit: USC/Lozito Lab

“This study has provided us with essential practice on how to improve an organism’s regenerative potential,” said Lozito. “Perfecting the imperfect regenerated lizard tail provides us with a blueprint for improving healing in wounds that don’t naturally regenerate, such as severed human limbs and spinal cords. In this way, we hope our lizard research will lead to medical breakthroughs for treating hard-to-heal injuries.”

Reference: “Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells” by Thomas P. Lozito, Ricardo Londono, Aaron X. Sun and Megan L. Hudnall, 14 October 2021, Nature Communications.
DOI: 10.1038/s41467-021-26321-9

Additional co-authors include Ricardo Londono and Aaron X. Sun from the University of Pittsburgh School of Medicine, and Megan L. Hudnall from USC.

The work was made possible by grant R01GM115444 from the National Institute of General Medical Sciences, one of the National Institutes of Health.

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