Document Detail


Endothelial cell phenotypic behaviors cluster into dynamic state transition programs modulated by angiogenic and angiostatic cytokines.
MedLine Citation:
PMID:  23303249     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Angiogenesis requires coordinated dynamic regulation of multiple phenotypic behaviors of endothelial cells in response to environmental cues. Multi-scale computational models of angiogenesis can be useful for analyzing effects of cell behaviors on the tissue level outcome, but these models require more intensive experimental studies dedicated to determining the required quantitative "rules" for cell-level phenotypic responses across a landscape of pro- and anti-angiogenic stimuli in order to ascertain how changes in these single cell responses lead to emerging multi-cellular behavior such as sprout formation. Here we employ single-cell microscopy to ascertain phenotypic behaviors of more than 800 human microvascular endothelial cells under various combinational angiogenic (VEGF) and angiostatic (PF4) cytokine treatments, analyzing their dynamic behavioral transitions among sessile, migratory, proliferative, and apoptotic states. We find that an endothelial cell population clusters into an identifiable set of a few distinct phenotypic state transition patterns (clusters) that is consistent across all cytokine conditions. Varying the cytokine conditions, such as VEGF and PF4 combinations here, modulates the proportion of the population following a particular pattern (referred to as phenotypic cluster weights) without altering the transition dynamics within the patterns. We then map the phenotypic cluster weights to quantified population level sprout densities using a multi-variate regression approach, and identify linear combinations of the phenotypic cluster weights that associate with greater or lesser sprout density across the various treatment conditions. VEGF-dominant cytokine combinations yielding high sprout densities are characterized by high proliferative and low apoptotic cluster weights, whereas PF4-dominant conditions yielding low sprout densities are characterized by low proliferative and high apoptotic cluster weights. Migratory cluster weights show only mild association with sprout density outcomes under the VEGF/PF4 conditions and the sprout formation characteristics explored here.
Authors:
Tharathorn Rimchala; Roger D Kamm; Douglas A Lauffenburger
Related Documents :
24721049 - Preparation, antiangiogenic and antitumoral activities of the chemically sulfated gluca...
23295879 - The influence of carbohydrates in the interaction of paracoccidioides brasiliensis with...
25064659 - Mathematical modelling of cancer invasion: implications of cell adhesion variability fo...
24368809 - Clasp2 interacts with p120-catenin and governs microtubule dynamics at adherens junctions.
24508729 - High proliferative potential endothelial colony forming cells contribute to hypoxia-ind...
21536769 - Isolation of human capillary endothelial cells from abdominal adipose tissue.
7520889 - Novel psi-s-ch2 peptide-bond replacement and its utilization in the synthesis of nonpep...
7741679 - Is laparoscopy associated with a lower rate of postoperative adhesions than laparotomy?...
16864799 - Liprin-alpha is required for photoreceptor target selection in drosophila.
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Integrative biology : quantitative biosciences from nano to macro     Volume:  5     ISSN:  1757-9708     ISO Abbreviation:  Integr Biol (Camb)     Publication Date:  2013 Mar 
Date Detail:
Created Date:  2013-02-25     Completed Date:  2013-09-24     Revised Date:  2014-03-07    
Medline Journal Info:
Nlm Unique ID:  101478378     Medline TA:  Integr Biol (Camb)     Country:  England    
Other Details:
Languages:  eng     Pagination:  510-22     Citation Subset:  IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Algorithms
Apoptosis
Cell Culture Techniques
Cell Movement
Cell Proliferation
Cluster Analysis
Collagen / metabolism
Cytokines / metabolism*
Endothelial Cells / cytology*
Endothelium, Vascular / metabolism
Humans
Microcirculation
Models, Biological
Multivariate Analysis
Neovascularization, Pathologic*
Phenotype
Regression Analysis
Grant Support
ID/Acronym/Agency:
R01 EB010246/EB/NIBIB NIH HHS; R01 GM081336/GM/NIGMS NIH HHS; R01-EB010246/EB/NIBIB NIH HHS; R01-GM081336/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Cytokines; 9007-34-5/Collagen
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Femtomolar Zn(ii) affinity of minimal zinc hook peptides - a promising small tag for protein enginee...
Next Document:  Sequential steps in DNA replication are inhibited to ensure reduction of ploidy in meiosis.