Cargando…
Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders
The developing forelimb has been a foundational model to understand how specified progenitor cells integrate genetic information to produce the tetrapod limb bauplan. Although the reigning hypothesis is that all tetrapods develop limbs in a similar manner, recent work suggests that urodeles have evo...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010949/ https://www.ncbi.nlm.nih.gov/pubmed/35433673 http://dx.doi.org/10.3389/fcell.2022.797352 |
_version_ | 1784687589551243264 |
---|---|
author | Purushothaman, Sruthi Lopez Aviña, Brianda B. Seifert, Ashley W. |
author_facet | Purushothaman, Sruthi Lopez Aviña, Brianda B. Seifert, Ashley W. |
author_sort | Purushothaman, Sruthi |
collection | PubMed |
description | The developing forelimb has been a foundational model to understand how specified progenitor cells integrate genetic information to produce the tetrapod limb bauplan. Although the reigning hypothesis is that all tetrapods develop limbs in a similar manner, recent work suggests that urodeles have evolved a derived mode of limb dvelopment. Here, we demonstrate through pharmacological and genetic inactivation of Sonic hedgehog (Shh) signaling in axolotls that Shh directs expansion and survival of limb progenitor cells in addition to patterning the limb across the proximodistal and antero-posterior axis. In contrast to inactivation of Shh in mouse or chick embryos where a humerus, radius, and single digit develop, Shh crispant axolotls completely lack forelimbs. In rescuing limb development by implanting SHH-N protein beads into the nascent limb field of Shh crispants, we show that the limb field is specified in the absence of Shh and that hedgehog pathway activation is required to initiate proximodistal outgrowth. When our results are examined alongside other derived aspects of salamander limb development and placed in a phylogenetic context, a new hypothesis emerges whereby the ability for cells at an amputation plane to activate morphogenesis and regenerate a limb may have evolved uniquely in urodeles. |
format | Online Article Text |
id | pubmed-9010949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90109492022-04-16 Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders Purushothaman, Sruthi Lopez Aviña, Brianda B. Seifert, Ashley W. Front Cell Dev Biol Cell and Developmental Biology The developing forelimb has been a foundational model to understand how specified progenitor cells integrate genetic information to produce the tetrapod limb bauplan. Although the reigning hypothesis is that all tetrapods develop limbs in a similar manner, recent work suggests that urodeles have evolved a derived mode of limb dvelopment. Here, we demonstrate through pharmacological and genetic inactivation of Sonic hedgehog (Shh) signaling in axolotls that Shh directs expansion and survival of limb progenitor cells in addition to patterning the limb across the proximodistal and antero-posterior axis. In contrast to inactivation of Shh in mouse or chick embryos where a humerus, radius, and single digit develop, Shh crispant axolotls completely lack forelimbs. In rescuing limb development by implanting SHH-N protein beads into the nascent limb field of Shh crispants, we show that the limb field is specified in the absence of Shh and that hedgehog pathway activation is required to initiate proximodistal outgrowth. When our results are examined alongside other derived aspects of salamander limb development and placed in a phylogenetic context, a new hypothesis emerges whereby the ability for cells at an amputation plane to activate morphogenesis and regenerate a limb may have evolved uniquely in urodeles. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9010949/ /pubmed/35433673 http://dx.doi.org/10.3389/fcell.2022.797352 Text en Copyright © 2022 Purushothaman, Lopez Aviña and Seifert. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Purushothaman, Sruthi Lopez Aviña, Brianda B. Seifert, Ashley W. Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders |
title |
Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders |
title_full |
Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders |
title_fullStr |
Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders |
title_full_unstemmed |
Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders |
title_short |
Sonic hedgehog is Essential for Proximal-Distal Outgrowth of the Limb Bud in Salamanders |
title_sort | sonic hedgehog is essential for proximal-distal outgrowth of the limb bud in salamanders |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010949/ https://www.ncbi.nlm.nih.gov/pubmed/35433673 http://dx.doi.org/10.3389/fcell.2022.797352 |
work_keys_str_mv | AT purushothamansruthi sonichedgehogisessentialforproximaldistaloutgrowthofthelimbbudinsalamanders AT lopezavinabriandab sonichedgehogisessentialforproximaldistaloutgrowthofthelimbbudinsalamanders AT seifertashleyw sonichedgehogisessentialforproximaldistaloutgrowthofthelimbbudinsalamanders |