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Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process
We crafted human immunodeficiency virus (HIV)-like particles of diameter about 140 nm, which expressed two major HIV-1 proteins, namely, env and gag gene products, and used this reagent to simulate the rate of decay of HIV from the blood stream of BALB/c male mice. We found that most (~90%) of the p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256111/ https://www.ncbi.nlm.nih.gov/pubmed/28167948 http://dx.doi.org/10.3389/fimmu.2017.00035 |
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author | Mates, Jessica M. Yao, Zhili Cheplowitz, Alana M. Suer, Ozan Phillips, Gary S. Kwiek, Jesse J. Rajaram, Murugesan V. S. Kim, Jonghan Robinson, John M. Ganesan, Latha P. Anderson, Clark L. |
author_facet | Mates, Jessica M. Yao, Zhili Cheplowitz, Alana M. Suer, Ozan Phillips, Gary S. Kwiek, Jesse J. Rajaram, Murugesan V. S. Kim, Jonghan Robinson, John M. Ganesan, Latha P. Anderson, Clark L. |
author_sort | Mates, Jessica M. |
collection | PubMed |
description | We crafted human immunodeficiency virus (HIV)-like particles of diameter about 140 nm, which expressed two major HIV-1 proteins, namely, env and gag gene products, and used this reagent to simulate the rate of decay of HIV from the blood stream of BALB/c male mice. We found that most (~90%) of the particles were eliminated (cleared) from the blood by the liver sinusoidal endothelial cells (LSECs), the remainder from Kupffer cells; suggesting that LSECs are the major liver scavengers for HIV clearance from blood. Decay was rapid with kinetics suggesting second order with respect to particles, which infers dimerization of a putative receptor on LSEC. The number of HIV-like particles required for saturating the clearance mechanism was approximated. The capacity for elimination of blood-borne HIV-like particles by the sinusoid was 112 million particles per minute. Assuming that the sinusoid endothelial cells were about the size of glass-adherent macrophages, then elimination capacity was more than 540 particles per hour per endothelial cell. |
format | Online Article Text |
id | pubmed-5256111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52561112017-02-06 Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process Mates, Jessica M. Yao, Zhili Cheplowitz, Alana M. Suer, Ozan Phillips, Gary S. Kwiek, Jesse J. Rajaram, Murugesan V. S. Kim, Jonghan Robinson, John M. Ganesan, Latha P. Anderson, Clark L. Front Immunol Immunology We crafted human immunodeficiency virus (HIV)-like particles of diameter about 140 nm, which expressed two major HIV-1 proteins, namely, env and gag gene products, and used this reagent to simulate the rate of decay of HIV from the blood stream of BALB/c male mice. We found that most (~90%) of the particles were eliminated (cleared) from the blood by the liver sinusoidal endothelial cells (LSECs), the remainder from Kupffer cells; suggesting that LSECs are the major liver scavengers for HIV clearance from blood. Decay was rapid with kinetics suggesting second order with respect to particles, which infers dimerization of a putative receptor on LSEC. The number of HIV-like particles required for saturating the clearance mechanism was approximated. The capacity for elimination of blood-borne HIV-like particles by the sinusoid was 112 million particles per minute. Assuming that the sinusoid endothelial cells were about the size of glass-adherent macrophages, then elimination capacity was more than 540 particles per hour per endothelial cell. Frontiers Media S.A. 2017-01-24 /pmc/articles/PMC5256111/ /pubmed/28167948 http://dx.doi.org/10.3389/fimmu.2017.00035 Text en Copyright © 2017 Mates, Yao, Cheplowitz, Suer, Phillips, Kwiek, Rajaram, Kim, Robinson, Ganesan and Anderson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Mates, Jessica M. Yao, Zhili Cheplowitz, Alana M. Suer, Ozan Phillips, Gary S. Kwiek, Jesse J. Rajaram, Murugesan V. S. Kim, Jonghan Robinson, John M. Ganesan, Latha P. Anderson, Clark L. Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process |
title | Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process |
title_full | Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process |
title_fullStr | Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process |
title_full_unstemmed | Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process |
title_short | Mouse Liver Sinusoidal Endothelium Eliminates HIV-Like Particles from Blood at a Rate of 100 Million per Minute by a Second-Order Kinetic Process |
title_sort | mouse liver sinusoidal endothelium eliminates hiv-like particles from blood at a rate of 100 million per minute by a second-order kinetic process |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256111/ https://www.ncbi.nlm.nih.gov/pubmed/28167948 http://dx.doi.org/10.3389/fimmu.2017.00035 |
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