help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chow, D. C.
Right arrow Articles by Papoutsakis, E. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chow, D. C.
Right arrow Articles by Papoutsakis, E. T.

Biophys J, August 2001, p. 685-696, Vol. 81, No. 2

Modeling pO2 Distributions in the Bone Marrow Hematopoietic Compartment. II. Modified Kroghian Models

Dominic C. Chow, Larissa A. Wenning, William M. Miller, and E. Terry Papoutsakis

Department of Chemical Engineering, Northwestern University, Evanston, Illinois 60208-3120 USA

Hematopoietic cells of various lineages are organized in distinct cellular architectures in the bone marrow hematopoietic compartment (BMHC). The homogeneous Kroghian model, which deals only with a single cell type, may not be sufficient to accurately describe oxygen transfer in the BMHC. Thus, for cellular architectures of physiological significance, more complex biophysical-transport models were considered and compared against simulations using the homogeneous Kroghian model. The effects of the heterogeneity of model parameters on the oxygen tension (pO2) distribution were examined using the multilayer Kroghian model. We have also developed two-dimensional Kroghian models to simulate several cellular architectures in which a cell cluster (erythroid cluster) or an individual cell (megakaryocyte or adipocyte) is located in the BMHC predominantly occupied by mature granulocytes. pO2 distributions in colony-type cellular arrangements (erythroblastic islets, granulopoietic loci, and lymphocytic nodules) in the BMHC were also evaluated by modifying the multilayer Kroghian model. The simulated results indicate that most hematopoietic progenitors experience low pO2 values, which agrees with the finding that low pO2 promotes the expansion of various hematopoietic progenitors. These results suggest that the most primitive stem cells, which are located even further away from BM sinuses, are likely located in a very low pO2 environment.

Biophys J, August 2001, p. 685-696, Vol. 81, No. 2
© 2001 by the Biophysical Society   0006-3495/01/08/685/12  $2.00



This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
S. M. Schieke, M. Ma, L. Cao, J. P. McCoy Jr., C. Liu, N. F. Hensel, A. J. Barrett, M. Boehm, and T. Finkel
Mitochondrial Metabolism Modulates Differentiation and Teratoma Formation Capacity in Mouse Embryonic Stem Cells
J. Biol. Chem., October 17, 2008; 283(42): 28506 - 28512.
[Abstract] [Full Text] [PDF]


Home page
JEMHome page
C. Chen, Y. Liu, R. Liu, T. Ikenoue, K.-L. Guan, Y. Liu, and P. Zheng
TSC-mTOR maintains quiescence and function of hematopoietic stem cells by repressing mitochondrial biogenesis and reactive oxygen species
J. Exp. Med., September 29, 2008; 205(10): 2397 - 2408.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
O. Krejci, M. Wunderlich, H. Geiger, F.-S. Chou, D. Schleimer, M. Jansen, P. R. Andreassen, and J. C. Mulloy
p53 signaling in response to increased DNA damage sensitizes AML1-ETO cells to stress-induced death
Blood, February 15, 2008; 111(4): 2190 - 2199.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
J. L. Chan, K. C. Tang, A. P. Patel, L. M. Bonilla, N. Pierobon, N. M. Ponzio, and P. Rameshwar
Antigen-presenting property of mesenchymal stem cells occurs during a narrow window at low levels of interferon-{gamma}
Blood, June 15, 2006; 107(12): 4817 - 4824.
[Abstract] [Full Text] [PDF]


Home page
Stem CellsHome page
Z. Ivanovic, F. Hermitte, P. B. de la Grange, B. Dazey, F. Belloc, F. Lacombe, G. Vezon, and V. Praloran
Simultaneous Maintenance of Human Cord Blood SCID-Repopulating Cells and Expansion of Committed Progenitors at Low O2 Concentration (3%)
Stem Cells, September 1, 2004; 22(5): 716 - 724.
[Abstract] [Full Text] [PDF]


Home page
JBJSHome page
G. F. Muschler, C. Nakamoto, and L. G. Griffith
Engineering Principles of Clinical Cell-Based Tissue Engineering
J. Bone Joint Surg. Am., July 1, 2004; 86(7): 1541 - 1558.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. A. Potian, H. Aviv, N. M. Ponzio, J. S. Harrison, and P. Rameshwar
Veto-Like Activity of Mesenchymal Stem Cells: Functional Discrimination Between Cellular Responses to Alloantigens and Recall Antigens
J. Immunol., October 1, 2003; 171(7): 3426 - 3434.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
D. L. Hevehan, W. M. Miller, and E. T. Papoutsakis
Differential expression and phosphorylation of distinct STAT3 proteins during granulocytic differentiation
Blood, March 1, 2002; 99(5): 1627 - 1637.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the Biophysical Society.