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Thymosin β4 dynamics during chicken enteroid development

The sheared avian intestinal villus-crypts exhibit high tendency to self-repair and develop enteroids in culture. Presuming that this transition process involves differential biomolecular changes, we employed matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF–MS)...

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Autores principales: Acharya, Mohan, Liyanage, Rohana, Gupta, Anamika, Arsi, Komala, Donoghue, Ann M., Lay, Jackson O., Rath, Narayan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873109/
https://www.ncbi.nlm.nih.gov/pubmed/33301106
http://dx.doi.org/10.1007/s11010-020-04008-x
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author Acharya, Mohan
Liyanage, Rohana
Gupta, Anamika
Arsi, Komala
Donoghue, Ann M.
Lay, Jackson O.
Rath, Narayan C.
author_facet Acharya, Mohan
Liyanage, Rohana
Gupta, Anamika
Arsi, Komala
Donoghue, Ann M.
Lay, Jackson O.
Rath, Narayan C.
author_sort Acharya, Mohan
collection PubMed
description The sheared avian intestinal villus-crypts exhibit high tendency to self-repair and develop enteroids in culture. Presuming that this transition process involves differential biomolecular changes, we employed matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF–MS) to find whether there were differences in the spectral profiles of sheared villi versus the enteroids, assessed in the mass range of 2–18 kDa. The results showed substantial differences in the intensities of the spectral peaks, one particularly corresponding to the mass of 4963 Da, which was significantly low in the sheared villus-crypts compared with the enteroids. Based on our previous results with other avian tissues and further molecular characterization by LC-ESI-IT-TOF–MS, and multiple reaction monitoring (MRM), the peak was identified to be thymosin β4 (Tβ4), a ubiquitously occurring regulatory peptide implicated in wound healing process. The identity of the peptide was further confirmed by immunohistochemistry which showed it to be present in a very low levels in the sheared villi but replete in the enteroids. Since Tβ4 sequesters G-actin preventing its polymerization to F-actin, we compared the changes in F-actin by its immunohistochemical localization that showed no significant differences between the sheared villi and enteroids. We propose that depletion of Tβ4 likely precedes villous reparation process. The possible mechanism for the differences in Tβ4 profile in relation to the healing of the villus-crypts to developing enteroids is discussed.
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spelling pubmed-78731092021-02-22 Thymosin β4 dynamics during chicken enteroid development Acharya, Mohan Liyanage, Rohana Gupta, Anamika Arsi, Komala Donoghue, Ann M. Lay, Jackson O. Rath, Narayan C. Mol Cell Biochem Article The sheared avian intestinal villus-crypts exhibit high tendency to self-repair and develop enteroids in culture. Presuming that this transition process involves differential biomolecular changes, we employed matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF–MS) to find whether there were differences in the spectral profiles of sheared villi versus the enteroids, assessed in the mass range of 2–18 kDa. The results showed substantial differences in the intensities of the spectral peaks, one particularly corresponding to the mass of 4963 Da, which was significantly low in the sheared villus-crypts compared with the enteroids. Based on our previous results with other avian tissues and further molecular characterization by LC-ESI-IT-TOF–MS, and multiple reaction monitoring (MRM), the peak was identified to be thymosin β4 (Tβ4), a ubiquitously occurring regulatory peptide implicated in wound healing process. The identity of the peptide was further confirmed by immunohistochemistry which showed it to be present in a very low levels in the sheared villi but replete in the enteroids. Since Tβ4 sequesters G-actin preventing its polymerization to F-actin, we compared the changes in F-actin by its immunohistochemical localization that showed no significant differences between the sheared villi and enteroids. We propose that depletion of Tβ4 likely precedes villous reparation process. The possible mechanism for the differences in Tβ4 profile in relation to the healing of the villus-crypts to developing enteroids is discussed. Springer US 2020-12-10 2021 /pmc/articles/PMC7873109/ /pubmed/33301106 http://dx.doi.org/10.1007/s11010-020-04008-x Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Acharya, Mohan
Liyanage, Rohana
Gupta, Anamika
Arsi, Komala
Donoghue, Ann M.
Lay, Jackson O.
Rath, Narayan C.
Thymosin β4 dynamics during chicken enteroid development
title Thymosin β4 dynamics during chicken enteroid development
title_full Thymosin β4 dynamics during chicken enteroid development
title_fullStr Thymosin β4 dynamics during chicken enteroid development
title_full_unstemmed Thymosin β4 dynamics during chicken enteroid development
title_short Thymosin β4 dynamics during chicken enteroid development
title_sort thymosin β4 dynamics during chicken enteroid development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873109/
https://www.ncbi.nlm.nih.gov/pubmed/33301106
http://dx.doi.org/10.1007/s11010-020-04008-x
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