» Articles » PMID: 23447666

Ectopic Eyes Outside the Head in Xenopus Tadpoles Provide Sensory Data for Light-mediated Learning

Overview
Journal J Exp Biol
Specialty Biology
Date 2013 Mar 1
PMID 23447666
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

A major roadblock in the biomedical treatment of human sensory disorders, including blindness, has been an incomplete understanding of the nervous system and its ability to adapt to changes in sensory modality. Likewise, fundamental insight into the evolvability of complex functional anatomies requires understanding brain plasticity and the interaction between the nervous system and body architecture. While advances have been made in the generation of artificial and biological replacement components, the brain's ability to interpret sensory information arising from ectopic locations is not well understood. We report the use of eye primordia grafts to create ectopic eyes along the body axis of Xenopus tadpoles. These eyes are morphologically identical to native eyes and can be induced at caudal locations. Cell labeling studies reveal that eyes created in the tail send projections to the stomach and trunk. To assess function we performed light-mediated learning assays using an automated machine vision and environmental control system. The results demonstrate that ectopic eyes in the tail of Xenopus tadpoles could confer vision to the host. Thus ectopic visual organs were functional even when present at posterior locations. These data and protocols demonstrate the ability of vertebrate brains to interpret sensory input from ectopic structures and incorporate them into adaptive behavioral programs. This tractable new model for understanding the robust plasticity of the central nervous system has significant implications for regenerative medicine and sensory augmentation technology.

Citing Articles

Evolutionary Implications of Self-Assembling Cybernetic Materials with Collective Problem-Solving Intelligence at Multiple Scales.

Hartl B, Risi S, Levin M Entropy (Basel). 2024; 26(7).

PMID: 39056895 PMC: 11275831. DOI: 10.3390/e26070532.


Self-Improvising Memory: A Perspective on Memories as Agential, Dynamically Reinterpreting Cognitive Glue.

Levin M Entropy (Basel). 2024; 26(6).

PMID: 38920491 PMC: 11203334. DOI: 10.3390/e26060481.


Bilateral Retinofugal Pathfinding Impairments Limit Behavioral Compensation in Near-Congenital One-Eyed .

Forsthofer M, Gordy C, Kolluri M, Straka H eNeuro. 2024; 11(1).

PMID: 38164595 PMC: 10849038. DOI: 10.1523/ENEURO.0371-23.2023.


retinal ganglion cell axon extension is unaffected by 5-HT receptor activation during visual system development.

Basakis P, Khaderi A, Lom B MicroPubl Biol. 2023; 2023.

PMID: 38116474 PMC: 10728752. DOI: 10.17912/micropub.biology.001076.


Future medicine: from molecular pathways to the collective intelligence of the body.

Lagasse E, Levin M Trends Mol Med. 2023; 29(9):687-710.

PMID: 37481382 PMC: 10527237. DOI: 10.1016/j.molmed.2023.06.007.


References
1.
Yang B, Yan G, Yan R . [A review of brain-computer interfaces (BCIs)]. Zhongguo Yi Liao Qi Xie Za Zhi. 2006; 29(5):353-7. View

2.
Schneuwly S, Klemenz R, Gehring W . Redesigning the body plan of Drosophila by ectopic expression of the homoeotic gene Antennapedia. Nature. 1987; 325(6107):816-8. DOI: 10.1038/325816a0. View

3.
Korf H, Liesner R, Meissl H, Kirk A . Pineal complex of the clawed toad, Xenopus laevis Daud.: structure and function. Cell Tissue Res. 1981; 216(1):113-30. DOI: 10.1007/BF00234548. View

4.
Constantine-Paton M, Caprianica R . Central projection of optic tract from translocated eyes in the leopard frog (Rana pipiens). Science. 1975; 189(4201):480-2. DOI: 10.1126/science.50621. View

5.
Lupo G, Liu Y, Qiu R, Chandraratna R, Barsacchi G, He R . Dorsoventral patterning of the Xenopus eye: a collaboration of Retinoid, Hedgehog and FGF receptor signaling. Development. 2005; 132(7):1737-48. DOI: 10.1242/dev.01726. View