4.7 Article

A Comparative Study of Canine Mesenchymal Stem Cells Isolated from Different Sources

期刊

ANIMALS
卷 12, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/ani12121502

关键词

canine mesenchymal stem cells; morphology; phenotype; multilineage potential

资金

  1. Slovak Research and Development Agency [APVV-19-0193]
  2. Scientific Grant Agency of the Ministry of Education Slovak Republic [VEGA 1/0285/22]

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This study compares the differences in morphology, phenotype, multilineage potential, and proliferation capacity of canine MSCs isolated from bone marrow, adipose tissue, and amniotic tissue. The results show variations in these characteristics among the MSCs from different sources, and suggest considerations for isolation, expansion, and phenotyping of these cells prior to their application in regenerative veterinary medicine.
Simple Summary The present study describes differences in the isolation yield, morphology, presence of surface markers and proliferation capacity but not in the multilineage potential of canine MSCs isolated from bone marrow, adipose tissue and amnion. Among all the MSCs analysed, AT-MSCs showed the highest isolation yield, phenotype homogeneity, proliferation capacity and osteogenic and chondrogenic potential. In addition, for BM-MSCs and AM-MSCs, we uncovered some differences that need to be considered during isolation, expansion and phenotyping prior to their possible application in targeted regenerative veterinary medicine. In this study, we provide comprehensive analyses of mesenchymal stem cells (MSCs) isolated from three types of canine tissues: bone marrow (BM-MSCs), adipose tissue (AT-MSCs) and amniotic tissue (AM-MSCs). We compare their morphology, phenotype, multilineage potential and proliferation activity. The BM-MSCs and AM-MSCs showed fibroblast-like shapes against the spindle shape of the AT-MSCs. All populations showed strong osteogenic and chondrogenic potential. However, we observed phenotypic differences. The BM-MSCs and AT-MSCs revealed high expression of CD29, CD44, CD90 and CD105 positivity compared to the AM-MSCs, which showed reduced expression of all the analysed CD markers. Similarly, the isolation yield and proliferation varied depending on the source. The highest isolation yield and proliferation were detected in the population of AT-MSCs, while the AM-MSCs showed a high yield of cells, but the lowest proliferation activity, in contrast to the BM-MSCs which had the lowest isolation yield. Thus, the present data provide assumptions for obtaining a homogeneous MSC derived from all three canine tissues for possible applications in veterinary regenerative medicine, while the origin of isolated MSCs must always be taken into account.

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