Analyze Diet
Theriogenology2017; 100; 8-15; doi: 10.1016/j.theriogenology.2017.05.015

A proteomic study of mesenchymal stem cells from equine umbilical cord.

Abstract: To the best of our knowledge, this is the first study describing the proteome of equine umbilical cord intervascular matrix mesenchymal stem cells (UCIM-MSCs) in a global and functional manner. The aim of this work was to analyze the proteome of previously characterized UCIM-MSCs to determine protein abundance and classify the identified proteins according to Gene Ontology (GO) terms. Protein classification analysis according to biological process, molecular function and cellular component was performed using the PANTHER (Protein ANalysis THrough Evolutionary Relationships) Classification System, which revealed enrichment for 42 biological processes, 23 molecular functions and 18 cellular components. Protein abundance was estimated according to the emPAI method (Exponential Modified Protein Abundance Index). The two most abundant proteins in the proteome of UCIM-MSCs were the cytoskeletal proteins actin and vimentin, which have important roles in cell stability and motility. Additionally, we identified 14 cell surface antigens. Three of them, CD44, CD90 and CD105, had been previously validated by flow cytometry. In the present study, we also identified important information about the biological properties of UCIM-MSCs such as differentiation potential, low immunogenicity (low MHC-II expression) and chromosomal stability, which reinforces their use for cell therapy. Together with the proteomic findings, this information allowed us to infer the functional relevance of several activities related to primary metabolic processes, protein synthesis, production of vesicle coats, vesicle-mediated transport and antioxidant activity. In addition, the identification of different cell surface markers may help establish an immunophenotypic panel suitable for the characterization of MSCs from equine fetal membranes.
Publication Date: 2017-05-24 PubMed ID: 28708537DOI: 10.1016/j.theriogenology.2017.05.015Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research focuses on the proteomic study of mesenchymal stem cells obtained from the intervascular matrix of equine umbilical cord (UCIM-MSCs). This is the first study to identify and analyze these proteins and their functions, revealing significant factors such as cellular stability, mobility, and low immunogenicity, thereby emphasizing their potential application in cell therapy.

Understanding the Proteome of UCIM-MSCs

  • The main aim was to study the proteome of the previously characterized UCIM-MSCs. Proteome represents all proteins expressed by a cell. Understanding the proteome helps identify the presence and abundance of different proteins and their associated functions.
  • The researchers classified the identified proteins based on Gene Ontology (GO) terms. These terms provide information about biological process, molecular function, and cellular components associated with the proteins.
  • The PANTHER (Protein ANalysis THrough Evolutionary Relationships) Classification System was used in the study; it disclosed enrichment for 42 biological processes, 23 molecular functions, and 18 cellular components.

Protein Abundance and Functions

  • The Exponential Modified Protein Abundance Index (emPAI) method was used to estimate the protein abundance. It helped identify the most prevalent proteins in the stem cells.
  • The two most abundant proteins were actin and vimentin, both of which are cytoskeletal proteins that play crucial roles in cell stability and mobility.
  • Besides, the study identified 14 cell surface antigens. Three of them, namely CD44, CD90, and CD105 had been previously validated by flow cytometry, a method used to measure physical and chemical characteristics of cells or particles.

UCIM-MSCs and their Therapeutic Potential

  • The study highlights the potential of UCIM-MSCs in cell therapy by presenting information about their biological properties such as differentiation potential, low immunogenicity (low MHC-II expression), and chromosomal stability.
  • It also emphasizes the importance of functions related to primary metabolic processes, protein synthesis, production of vesicle coats, vesicle-mediated transport, and antioxidant activity.
  • The identification of cell surface markers could help establish an immunophenotypic panel that aids the characterization of MSCs from equine fetal membranes, contributing to its therapeutic application.

Cite This Article

APA
Maia L, de Moraes CN, Dias MC, Martinez JB, Caballol AO, Testoni G, de Queiroz CM, Peña RD, Landim-Alvarenga FC, de Oliveira E. (2017). A proteomic study of mesenchymal stem cells from equine umbilical cord. Theriogenology, 100, 8-15. https://doi.org/10.1016/j.theriogenology.2017.05.015

Publication

ISSN: 1879-3231
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 100
Pages: 8-15
PII: S0093-691X(17)30254-6

Researcher Affiliations

Maia, Leandro
  • Department of Animal Reproduction and Veterinary Radiology, School of Veterinary Medicine and Animal Science, São Paulo State University UNESP, Botucatu, São Paulo 18618-681, Brazil; Proteomics Platform, Parc Cientific de Barcelona (PCB), Barcelona 08028, Spain. Electronic address: leandromvet@hotmail.com.
de Moraes, Carolina Nogueira
  • Department of Animal Reproduction and Veterinary Radiology, School of Veterinary Medicine and Animal Science, São Paulo State University UNESP, Botucatu, São Paulo 18618-681, Brazil.
Dias, Marianne Camargos
  • Department of Animal Reproduction and Veterinary Radiology, School of Veterinary Medicine and Animal Science, São Paulo State University UNESP, Botucatu, São Paulo 18618-681, Brazil.
Martinez, Julia Bauzá
  • Proteomics Platform, Parc Cientific de Barcelona (PCB), Barcelona 08028, Spain.
Caballol, Antonia Odena
  • Proteomics Platform, Parc Cientific de Barcelona (PCB), Barcelona 08028, Spain.
Testoni, Giorgia
  • Institute for Research in Biomedicine (IRB), Barcelona 08028, Spain.
de Queiroz, Carla Martins
  • Department of Animal Reproduction and Veterinary Radiology, School of Veterinary Medicine and Animal Science, São Paulo State University UNESP, Botucatu, São Paulo 18618-681, Brazil.
Peña, Ramón Díaz
  • Proteomics Platform, Parc Cientific de Barcelona (PCB), Barcelona 08028, Spain.
Landim-Alvarenga, Fernanda C
  • Department of Animal Reproduction and Veterinary Radiology, School of Veterinary Medicine and Animal Science, São Paulo State University UNESP, Botucatu, São Paulo 18618-681, Brazil.
de Oliveira, Eliandre
  • Proteomics Platform, Parc Cientific de Barcelona (PCB), Barcelona 08028, Spain.

MeSH Terms

  • Animals
  • Gene Expression Regulation / physiology
  • Horses / physiology
  • Mesenchymal Stem Cells / metabolism
  • Proteome
  • Umbilical Cord / cytology

Citations

This article has been cited 6 times.
  1. Isaković J, Šerer K, Barišić B, Mitrečić D. Mesenchymal stem cell therapy for neurological disorders: The light or the dark side of the force?. Front Bioeng Biotechnol 2023;11:1139359.
    doi: 10.3389/fbioe.2023.1139359pubmed: 36926687google scholar: lookup
  2. Cai H, Guo H. Mesenchymal Stem Cells and Their Exocytotic Vesicles. Int J Mol Sci 2023 Jan 20;24(3).
    doi: 10.3390/ijms24032085pubmed: 36768406google scholar: lookup
  3. Do PT, Wu CC, Chiang YH, Hu CJ, Chen KY. Mesenchymal Stem/Stromal Cell Therapy in Blood-Brain Barrier Preservation Following Ischemia: Molecular Mechanisms and Prospects. Int J Mol Sci 2021 Sep 17;22(18).
    doi: 10.3390/ijms221810045pubmed: 34576209google scholar: lookup
  4. Gussenhoven R, Klein L, Ophelders DRMG, Habets DHJ, Giebel B, Kramer BW, Schurgers LJ, Reutelingsperger CPM, Wolfs TGAM. Annexin A1 as Neuroprotective Determinant for Blood-Brain Barrier Integrity in Neonatal Hypoxic-Ischemic Encephalopathy. J Clin Med 2019 Jan 24;8(2).
    doi: 10.3390/jcm8020137pubmed: 30682787google scholar: lookup
  5. Bundgaard L, Stensballe A, Elbæk KJ, Berg LC. Mapping of equine mesenchymal stromal cell surface proteomes for identification of specific markers using proteomics and gene expression analysis: an in vitro cross-sectional study. Stem Cell Res Ther 2018 Oct 25;9(1):288.
    doi: 10.1186/s13287-018-1041-8pubmed: 30359315google scholar: lookup
  6. Man RC, Idrus RBH, Ibrahim WIW, Saim AB, Lokanathan Y. Secretome Analysis of Human Nasal Fibroblast Identifies Proteins That Promote Wound Healing. Adv Exp Med Biol 2024;1450:59-76.
    doi: 10.1007/5584_2023_777pubmed: 37247133google scholar: lookup