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http://acervodigital.unesp.br/handle/11449/19741
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DC Field | Value | Language |
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dc.contributor.author | Pavon, L. F. | - |
dc.contributor.author | Gamarra, L. F. | - |
dc.contributor.author | Marti, L. C. | - |
dc.contributor.author | Amaro Junior, E. | - |
dc.contributor.author | Moreira-Filho, C. A. | - |
dc.contributor.author | Camargo-Mathias, M. I. | - |
dc.contributor.author | Okamoto, O. K. | - |
dc.date.accessioned | 2014-05-20T13:55:11Z | - |
dc.date.accessioned | 2016-10-25T17:05:00Z | - |
dc.date.available | 2014-05-20T13:55:11Z | - |
dc.date.available | 2016-10-25T17:05:00Z | - |
dc.date.issued | 2008-09-01 | - |
dc.identifier | http://dx.doi.org/10.1111/j.1365-2818.2008.02049.x | - |
dc.identifier.citation | Journal of Microscopy-oxford. Oxford: Blackwell Publishing, v. 231, n. 3, p. 374-383, 2008. | - |
dc.identifier.issn | 0022-2720 | - |
dc.identifier.issn | 1365-2818 | - |
dc.identifier.uri | http://hdl.handle.net/11449/19741 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/19741 | - |
dc.description.abstract | CD133 antigen is an integral membrane glycoprotein that can bind with different cells. Originally, however. this cellular surface antigen was expressed in human stem cells and in various cellular progenitors of the haematopoietic system. Human cord blood has been described as an excellent source of CD133(+) haematopoietic progenitor cells with a large application potential. One of the main objectives of the present study is to describe for the first time the ultrastructural characteristics of CD133(+) stem cells using transmission electronic microscopy. Another objective of the manuscript is to demonstrate through transmission electronic microscopy the molecular image of magnetic nanoparticles connected to the stein cells of great biotechnological importance, as well as demonstrating the value of this finding for electronic paramagnetic resonance and its related nanobioscientific value. Ultrastructural results showed the monoclonal antibody anti-CD133 bound to the superparamagnetic nanoparticles by the presence of electrondense granules in cell membrane, as well as in the cytoplasm, revealing the ultrastructural characteristics of CD133(+) cells, exhibiting a round morphology with discrete cytoplasmic projections, having an active nucleus that follows this morphology. The cellular cytoplasm was filled up with mitochondrias, as well as microtubules and vesicles pinocitic. characterizing the process as being related to internalization of the magnetic nanoparticles that were endocyted by the cells in question. Electronic paramagnetic resonance analysis of the CD133(+) stem cells detected that the small (spectrum) generated by the labelled cells comes from the superparamagnetic nanoparticles that are bound to them. These results strongly suggest that these CD133(+) cells can be used in nanobiotechnology applications, with benefits in different biomedical areas. | en |
dc.description.sponsorship | Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein SBIBHAE | - |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | - |
dc.format.extent | 374-383 | - |
dc.language.iso | eng | - |
dc.publisher | Blackwell Publishing | - |
dc.source | Web of Science | - |
dc.subject | magnetic nanoparticles | en |
dc.subject | nanobiotechnology | en |
dc.subject | stem cells | en |
dc.subject | ultrastructure | en |
dc.title | Ultrastructural characterization of CD133(+) stem cells bound to superparamagnetic nanoparticles: possible biotechnological applications | en |
dc.type | outro | - |
dc.contributor.institution | Albert Einstein Res & Educ Inst IEPAE | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.contributor.institution | Universidade Federal de São Paulo (UNIFESP) | - |
dc.description.affiliation | Albert Einstein Res & Educ Inst IEPAE, São Paulo, Brazil | - |
dc.description.affiliation | Univ São Paulo, Biotechnol Program, IPT, Butanan Inst, São Paulo, Brazil | - |
dc.description.affiliation | Univ São Paulo, Dept Radiol, São Paulo, Brazil | - |
dc.description.affiliation | Univ São Paulo, Dept Immunol, Inst Biomed Sci, São Paulo, Brazil | - |
dc.description.affiliation | UNESP, Biosci Inst, Dept Biol, Rio Claro, SP, Brazil | - |
dc.description.affiliation | Univ Fed São Paulo, Dept Neurol & Neurosurg, São Paulo, Brazil | - |
dc.description.affiliationUnesp | UNESP, Biosci Inst, Dept Biol, Rio Claro, SP, Brazil | - |
dc.description.sponsorshipId | SBIBHAE: (IIEP-AE 278-07 | - |
dc.description.sponsorshipId | FAPESP: 02/01826-5 | - |
dc.identifier.doi | 10.1111/j.1365-2818.2008.02049.x | - |
dc.identifier.wos | WOS:000259611000003 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | Journal of Microscopy-oxford | - |
dc.identifier.scopus | 2-s2.0-50649088630 | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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