» Articles » PMID: 27499877

Functional Joint Regeneration is Achieved Using Reintegration Mechanism in Xenopus Laevis

Overview
Date 2016 Aug 9
PMID 27499877
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

A functional joint requires integration of multiple tissues: the apposing skeletal elements should form an interlocking structure, and muscles should insert into skeletal tissues via tendons across the joint. Whereas newts can regenerate functional joints after amputation, Xenopus laevis regenerates a cartilaginous rod without joints, a "spike." Previously we reported that the reintegration mechanism between the remaining and regenerated tissues has a significant effect on regenerating joint morphogenesis during elbow joint regeneration in newt. Based on this insight into the importance of reintegration, we amputated frogs' limbs at the elbow joint and found that frogs could regenerate a functional elbow joint between the remaining tissues and regenerated spike. During regeneration, the regenerating cartilage was partially connected to the remaining articular cartilage to reform the interlocking structure of the elbow joint at the proximal end of the spike. Furthermore, the muscles of the remaining part inserted into the regenerated spike cartilage via tendons. This study might open up an avenue for analyzing molecular and cellular mechanisms of joint regeneration using Xenopus.

Citing Articles

FGF-stimulated tendon cells embrace a chondrogenic fate with BMP7 in newt tissue culture.

Sugiura N, Agata K Dev Growth Differ. 2024; 66(3):182-193.

PMID: 38342985 PMC: 11457504. DOI: 10.1111/dgd.12913.


Quantitative Image Processing for Three-Dimensional Episcopic Images of Biological Structures: Current State and Future Directions.

Holroyd N, Walsh C, Gourmet L, Walker-Samuel S Biomedicines. 2023; 11(3).

PMID: 36979887 PMC: 10045950. DOI: 10.3390/biomedicines11030909.


A comprehensive reference transcriptome resource for the Iberian ribbed newt Pleurodeles waltl, an emerging model for developmental and regeneration biology.

Matsunami M, Suzuki M, Haramoto Y, Fukui A, Inoue T, Yamaguchi K DNA Res. 2019; 26(3):217-229.

PMID: 31006799 PMC: 6589553. DOI: 10.1093/dnares/dsz003.


Changing While Staying the Same: Preservation of Structural Continuity During Limb Evolution by Developmental Integration.

Tsutsumi R, Tran M, Cooper K Integr Comp Biol. 2017; 57(6):1269-1280.

PMID: 28992070 PMC: 6455032. DOI: 10.1093/icb/icx092.

References
1.
Gardiner D, Endo T, Bryant S . The molecular basis of amphibian limb regeneration: integrating the old with the new. Semin Cell Dev Biol. 2002; 13(5):345-52. DOI: 10.1016/s1084952102000903. View

2.
Guo X, Day T, Jiang X, Garrett-Beal L, Topol L, Yang Y . Wnt/beta-catenin signaling is sufficient and necessary for synovial joint formation. Genes Dev. 2004; 18(19):2404-17. PMC: 522990. DOI: 10.1101/gad.1230704. View

3.
Holder N . Organization of connective tissue patterns by dermal fibroblasts in the regenerating axolotl limb. Development. 1989; 105(3):585-93. DOI: 10.1242/dev.105.3.585. View

4.
Schweitzer R, Chyung J, Murtaugh L, Brent A, Rosen V, Olson E . Analysis of the tendon cell fate using Scleraxis, a specific marker for tendons and ligaments. Development. 2001; 128(19):3855-66. DOI: 10.1242/dev.128.19.3855. View

5.
Ishibashi S, Cliffe R, Amaya E . Highly efficient bi-allelic mutation rates using TALENs in Xenopus tropicalis. Biol Open. 2013; 1(12):1273-6. PMC: 3558749. DOI: 10.1242/bio.20123228. View