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Regeneration of the dermal skeleton and wound epidermis formation depend on BMP signaling in the caudal fin of platyfish.

作者信息

Rees Lana, König Désirée, Jaźwińska Anna

机构信息

Department of Biology, University of Fribourg, Fribourg, Switzerland.

出版信息

Front Cell Dev Biol. 2023 Feb 9;11:1134451. doi: 10.3389/fcell.2023.1134451. eCollection 2023.


DOI:10.3389/fcell.2023.1134451
PMID:36846592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9946992/
Abstract

Fin regeneration has been extensively studied in zebrafish, a genetic model organism. Little is known about regulators of this process in distant fish taxa, such as the family, represented by the platyfish. Here, we used this species to investigate the plasticity of ray branching morphogenesis following either straight amputation or excision of ray triplets. This approach revealed that ray branching can be conditionally shifted to a more distal position, suggesting non-autonomous regulation of bone patterning. To gain molecular insights into regeneration of fin-specific dermal skeleton elements, actinotrichia and lepidotrichia, we localized expression of the genes and in the regenerative outgrowth. Blocking of the BMP type-I receptor suppressed phospho-Smad1/5 immunoreactivity, and impaired fin regeneration after blastema formation. The resulting phenotype was characterized by the absence of bone and actinotrichia restoration. In addition, the wound epidermis displayed extensive thickening. This malformation was associated with expanded Tp63 expression from the basal epithelium towards more superficial layers, suggesting abnormal tissue differentiation. Our data add to the increasing evidence for the integrative role of BMP signaling in epidermal and skeletal tissue formation during fin regeneration. This expands our understanding of common mechanisms guiding appendage restoration in diverse clades of teleosts.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/fa55cec9e64c/fcell-11-1134451-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/1e759fda1855/fcell-11-1134451-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/d78b140e90ea/fcell-11-1134451-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/7c408e667a56/fcell-11-1134451-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/c318b1e37a50/fcell-11-1134451-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/d7329e196b3b/fcell-11-1134451-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/d9807b81f4da/fcell-11-1134451-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/6ef348324f8a/fcell-11-1134451-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/fa55cec9e64c/fcell-11-1134451-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/1e759fda1855/fcell-11-1134451-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/d78b140e90ea/fcell-11-1134451-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/7c408e667a56/fcell-11-1134451-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/c318b1e37a50/fcell-11-1134451-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/d7329e196b3b/fcell-11-1134451-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/d9807b81f4da/fcell-11-1134451-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/6ef348324f8a/fcell-11-1134451-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/9946992/fa55cec9e64c/fcell-11-1134451-g008.jpg

相似文献

[1]
Regeneration of the dermal skeleton and wound epidermis formation depend on BMP signaling in the caudal fin of platyfish.

Front Cell Dev Biol. 2023-2-9

[2]
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[3]
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[4]
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[5]
Bone patterning is altered in the regenerating zebrafish caudal fin after ectopic expression of sonic hedgehog and bmp2b or exposure to cyclopamine.

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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Skeletal muscle regeneration after extensive cryoinjury of caudal myomeres in adult zebrafish.

NPJ Regen Med. 2024-2-20

[2]
Validity of Xiphophorus fish as models for human disease.

Dis Model Mech. 2024-1-1

本文引用的文献

[1]
Fin ray branching is defined by TRAP osteolytic tubules in zebrafish.

Proc Natl Acad Sci U S A. 2022-11-29

[2]
Platyfish bypass the constraint of the caudal fin ventral identity in teleosts.

Dev Dyn. 2022-11

[3]
Zebrafish fin regeneration involves generic and regeneration-specific osteoblast injury responses.

Elife. 2022-6-24

[4]
Hydrodynamic stress and phenotypic plasticity of the zebrafish regenerating fin.

J Exp Biol. 2021-8-1

[5]
Basal epidermis collective migration and local Sonic hedgehog signaling promote skeletal branching morphogenesis in zebrafish fins.

Dev Biol. 2021-9

[6]
Recent advancements in understanding fin regeneration in zebrafish.

Wiley Interdiscip Rev Dev Biol. 2020-1

[7]
Distribution and Restoration of Serotonin-Immunoreactive Paraneuronal Cells During Caudal Fin Regeneration in Zebrafish.

Front Mol Neurosci. 2019-9-19

[8]
Model systems for regeneration: zebrafish.

Development. 2019-9-20

[9]
Evolution of caudal fin ray development and caudal fin hypural diastema complex in spotted gar, teleosts, and other neopterygian fishes.

Dev Dyn. 2018-6

[10]
quantification of mechanical properties of caudal fins in adult zebrafish.

J Exp Biol. 2018-2-20

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