4.1 Article

Proteomic Analysis and Reprogramming Potential of the Porcine Intra-Ooplasmic Nanovesicles

Journal

CELLULAR REPROGRAMMING
Volume 25, Issue 5, Pages 238-250

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/cell.2023.0050

Keywords

oocytes; ooplasmic vesicles; nanovesicles; cell reprogramming; pluripotency

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This study isolated and characterized nanovesicles from mature porcine oocytes, which were named as intra-ooplasmic vesicles (IOVs) for the first time. Proteomic analysis revealed that these IOVs contained proteins related to reprogramming, antioxidative defense, cytoskeleton, heat shock proteins, and metabolism. Supplementing cultured fibroblasts with IOVs resulted in changes in cell morphology and the expression of pluripotency and trophoblastic markers.
Oocytes contain reprogramming machinery that can transform somatic cells into totipotent cells. In this study, we aimed to isolate and characterize nanovesicles from mature porcine oocytes and described them for the first time as intra-ooplasmic vesicles (IOVs). Isolated IOVs had an average diameter of 186.3 +/- 10.8 nm. Proteomic analysis revealed 467 peptide reads, with the top 20 proteins related to reprogramming, antioxidative defense, cytoskeleton, heat shock proteins, and metabolism. Protein-protein interaction and gene ontology analysis indicated that these proteins were involved in various biological pathways, including protein folding, metabolism, and cellular responses to stress. Supplementing cultured fibroblasts with IOVs resulted in the expression of the pluripotency marker OCT4 and the early trophoblastic marker CDX2 and increased expression of the corresponding mRNAs together with increasing KLF4 and SALL4 expression. IOV treatment of fibroblasts for 14 consecutive days resulted in changes in cell morphology, with increased expression of ZEB2 and YBX3 as markers for epithelial-to-mesenchymal transition (EMT). These results provide a rationale for further characterization of IOVs, investigation of potential reprogramming capabilities for EMT, and the generation of induced pluripotent or oligopotent stem cells.

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