Endothelial progenitor cells/endothelial cells (EPCs/ECs) have great potential to treat pathological conditions such as cardiac infarction, muscle ischemia, and bone fractures, but isolation of EPC/ECs from existing cell sources is challenging due to their low EC frequency. We have isolated endothelial progenitor (EP)-like cells from rat oral mucosa and characterized their yield, immunophenotype, growth, and in vivo angiogenic potential. The frequency of EP-like cells derived from oral mucosa is thousands of folds higher than EPCs derived from donor-match bone marrow samples. EP-like cells from oral mucosa were positive for EC markers CD31, VE-Cadherin, and VEGFR2. Oral mucosa-derived EP-like cells displayed robust uptake of acetylated low-density lipoprotein and formed stable capillary networks in Matrigel. Subcutaneously implanted oral mucosa-derived EP-like cells anastomosed with host blood vessels, implicating their ability to elicit angiogenesis. Similar to endothelial colony-forming cells, EP-like cells from oral mucosa have a significantly higher proliferative rate than human umbilical vein endothelial cells. These findings identify a putative EPC source that is easily accessible in the oral cavity, potentially from discarded tissue specimens, and yet with robust yield and potency for angiogenesis in tissue and organ regeneration.
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http://dx.doi.org/10.1089/scd.2016.0175 | DOI Listing |
Res Vet Sci
December 2021
Department of Veterinary Science, University of Parma, Strada del Taglio, 10, Parma 43126, Italy. Electronic address:
Mycoplasma hyopneumoniae is a major pathogen affecting pig herds and vaccination is the most utilized approach, despite providing partial protection. Age at vaccination, the delivery route, and vaccination protocol can influence vaccine efficacy. The influence of age and the presence of maternally-derived antibodies at vaccination on single-dose needle-less intradermal (ID) administration of an inactivated bacterin-based vaccine (Porcilis® M Hyo ID Once) were assessed in conventional pigs under field conditions.
View Article and Find Full Text PDFStem Cells Dev
January 2017
1 Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York.
Endothelial progenitor cells/endothelial cells (EPCs/ECs) have great potential to treat pathological conditions such as cardiac infarction, muscle ischemia, and bone fractures, but isolation of EPC/ECs from existing cell sources is challenging due to their low EC frequency. We have isolated endothelial progenitor (EP)-like cells from rat oral mucosa and characterized their yield, immunophenotype, growth, and in vivo angiogenic potential. The frequency of EP-like cells derived from oral mucosa is thousands of folds higher than EPCs derived from donor-match bone marrow samples.
View Article and Find Full Text PDFCytotechnology
May 2011
Institute of Atherosclerosis, Taishan Medical University, Taian, 271000, China.
Endothelial progenitor cells (EPCs) derived from bone marrow are known to be heterogeneous. In this study, we tried to find favorable conditions that induce the differentiation of mononuclear cells (MNCs) from bone marrow into EPCs. The differentiation capacity of MNCs from rat bone marrow was investigated in different conditions, such as different media, different induction times and different culture surfaces.
View Article and Find Full Text PDFShi Yan Sheng Wu Xue Bao
September 2002
Third Institute of Oceanography, SOA, Xiamen 361005.
Using immunohischemical method, we have localized for the first time in the amphioxus, Branchiostoma belcheri, neuropeptide Y (NPY)-like and beta-endorphin (beta-Ep)-like immunoreactivity in nervous system and Hatschek's pit. NPY-immunoreactive (-ir) perikarya appeared in the front and middle areas of the telencephalon and midbrain, as well as in the hindbrain. Dense plexuses of NPY-ir fibers coursed with NPY-ir neurons and formed fine networks.
View Article and Find Full Text PDFJ Immunol
January 1999
Institute of Molecular Medicine and Genetics, Medical College of Georgia, Augusta 30912, USA.
In the thymus, immature T cells are positively and negatively selected by multiple interactions between their Ag receptors (TCRs) and self MHC/peptide complexes expressed on thymic stromal cells. Here we show that in the milieu of negative selection on physiological self class II MHC/peptide complexes (Abwt), a single class II/peptide complex AbEp52-68 positively selects a number of TCRs with various Ag specificities. This TCR repertoire is semidiverse and not biased toward Ep-like Ags.
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