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Pregled bibliografske jedinice broj: 989758

Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription


Aliotta, Jason M.; Pereira, Mandy; Johnson, Kevin W.; de Paz, Nicole; Dooner, Mark S.; Puente, Napoleon; Ayala, Carol; Brilliant, Kate; Berz, David; Lee, David et al.
Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription // Experimental hematology, 38 (2010), 233-245 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 989758 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription

Autori
Aliotta, Jason M. ; Pereira, Mandy ; Johnson, Kevin W. ; de Paz, Nicole ; Dooner, Mark S. ; Puente, Napoleon ; Ayala, Carol ; Brilliant, Kate ; Berz, David ; Lee, David ; Ramratnam, Bharat ; McMillan, Paul N. ; Hixson, Douglas C. ; Josic, Djuro ; Quesenberry, Peter J.

Izvornik
Experimental hematology (0301-472X) 38 (2010); 233-245

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
HORIZONTAL TRANSFER ; MEMBRANE-VESICLES ; PLATELET MICROPARTICLES ; MULTIVESICULAR BODIES ; GENE-EXPRESSION ; HUMAN PLASMA ; EXOSOMES ; PROTEIN ; CANCER ; ENGRAFTMENT

Sažetak
Objective. Microvesicles have been shown to mediate intercellular communication. Previously, we have correlated entry of murine lung-derived microvesicles into murine bone marrow cells with expression of pulmonary epithelial cell-specific messenger RNA (mRNA) in these marrow cells. The present studies establish that entry of lung-derived microvesicles into marrow cells is a prerequisite for marrow expression of pulmonary epithelial cell-derived mRNA. Materials and Methods. Murine bone marrow cells cocultured with rat lung, but separated from them using a cell-impermeable membrane (0.4-mu m pore sire), were analyzed using species-specific printers (for rat or mouse). Results. These studies revealed that surfactant 13 and C mRNA produced by murine marrow cells were of both rat and mouse origin. Similar results were obtained using murine lung cocultured with rat bone marrow cells or when bone marrow cells were analyzed for the presence of Species-Specific albumin mRNA after coculture with rat or murine liver. These studies show that microvesicles both deliver mRNA to marrow cells and mediate marrow cell transcription of tissue-specific mRNA. The latter likely Underlies the longer-term stable change in genetic phenotype that has been observed. We have also observed microRNA in lung-derived microvesicles, and studies with RNase-treated microvesicles indicate that microRNA negatively modulates pulmonary epithelial cell-specific mRNA levels in cocultured marrow cells. In addition, we have also observed tissue-specific expression of brain, heart, and liver mRNA in cocultured marrow cells. suggesting that microvesicle-mediated cellular phenotype change is a universal phenomena. Conclusion. These studies suggest that cellular systems :are more phenotypically labile than previously considered. (C) 2010 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.

Izvorni jezik
Engleski

Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)



POVEZANOST RADA


Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju

Profili:

Avatar Url Đuro Josić (autor)


Citiraj ovu publikaciju:

Aliotta, Jason M.; Pereira, Mandy; Johnson, Kevin W.; de Paz, Nicole; Dooner, Mark S.; Puente, Napoleon; Ayala, Carol; Brilliant, Kate; Berz, David; Lee, David et al.
Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription // Experimental hematology, 38 (2010), 233-245 (međunarodna recenzija, članak, znanstveni)
Aliotta, J., Pereira, M., Johnson, K., de Paz, N., Dooner, M., Puente, N., Ayala, C., Brilliant, K., Berz, D. & Lee, D. (2010) Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription. Experimental hematology, 38, 233-245.
@article{article, author = {Aliotta, Jason M. and Pereira, Mandy and Johnson, Kevin W. and de Paz, Nicole and Dooner, Mark S. and Puente, Napoleon and Ayala, Carol and Brilliant, Kate and Berz, David and Lee, David and Ramratnam, Bharat and McMillan, Paul N. and Hixson, Douglas C. and Josic, Djuro and Quesenberry, Peter J.}, year = {2010}, pages = {233-245}, keywords = {HORIZONTAL TRANSFER, MEMBRANE-VESICLES, PLATELET MICROPARTICLES, MULTIVESICULAR BODIES, GENE-EXPRESSION, HUMAN PLASMA, EXOSOMES, PROTEIN, CANCER, ENGRAFTMENT}, journal = {Experimental hematology}, volume = {38}, issn = {0301-472X}, title = {Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription}, keyword = {HORIZONTAL TRANSFER, MEMBRANE-VESICLES, PLATELET MICROPARTICLES, MULTIVESICULAR BODIES, GENE-EXPRESSION, HUMAN PLASMA, EXOSOMES, PROTEIN, CANCER, ENGRAFTMENT} }
@article{article, author = {Aliotta, Jason M. and Pereira, Mandy and Johnson, Kevin W. and de Paz, Nicole and Dooner, Mark S. and Puente, Napoleon and Ayala, Carol and Brilliant, Kate and Berz, David and Lee, David and Ramratnam, Bharat and McMillan, Paul N. and Hixson, Douglas C. and Josic, Djuro and Quesenberry, Peter J.}, year = {2010}, pages = {233-245}, keywords = {HORIZONTAL TRANSFER, MEMBRANE-VESICLES, PLATELET MICROPARTICLES, MULTIVESICULAR BODIES, GENE-EXPRESSION, HUMAN PLASMA, EXOSOMES, PROTEIN, CANCER, ENGRAFTMENT}, journal = {Experimental hematology}, volume = {38}, issn = {0301-472X}, title = {Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription}, keyword = {HORIZONTAL TRANSFER, MEMBRANE-VESICLES, PLATELET MICROPARTICLES, MULTIVESICULAR BODIES, GENE-EXPRESSION, HUMAN PLASMA, EXOSOMES, PROTEIN, CANCER, ENGRAFTMENT} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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