Thymosin [beta]4 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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Veröffentlicht in:Molecular and cellular biochemistry 2020-12, Vol.476 (2), p.1303
Hauptverfasser: Acharya, Mohan, Liyanage, Rohana, Gupta, Anamika, Arsi, Komala, Donoghue, Ann M, Lay, Jackson O, Rath, Narayan C
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container_issue 2
container_start_page 1303
container_title Molecular and cellular biochemistry
container_volume 476
creator Acharya, Mohan
Liyanage, Rohana
Gupta, Anamika
Arsi, Komala
Donoghue, Ann M
Lay, Jackson O
Rath, Narayan C
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 [beta]4 (T[beta]4), 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 T[beta]4 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 T[beta]4 likely precedes villous reparation process. The possible mechanism for the differences in T[beta]4 profile in relation to the healing of the villus-crypts to developing enteroids is discussed.
doi_str_mv 10.1007/s11010-020-04008-x
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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 [beta]4 (T[beta]4), 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 T[beta]4 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 T[beta]4 likely precedes villous reparation process. 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subjects Comparative analysis
Ionization
Muscle proteins
Thymosin
title Thymosin [beta]4 dynamics during chicken enteroid development
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