Document Detail


Intercellular propagation of individually programmed growth bursts in FRTL-5 cells. Implications for interpreting growth factor actions.
MedLine Citation:
PMID:  2226304     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Five methods are commonly used to quantify FRTL-5 cells' and other thyrocytes' growth in vitro and the impact of growth inhibiting or stimulating maneuvers: Total cell count, mitotic index, DNA measurement, total [3H]thymidine incorporation, and the fraction of [3H]thymidine labeled cells. All of them assess cell growth as though all cells were homogeneous with an identical response to growth factors. We demonstrate here that this assumption is not valid. Rather, some intrinsically growth-prone cells appear to pass a growth signal to neighboring cells so that variably sized colonies of synchronized cells within each cluster growing from monodispersed cells are formed. This is true for FRTL-5 cells growing in vitro in monolayers and in three-dimensional, collagen embedded spheroids. The pattern is the same when cell suspensions or collagen-embedded spheroids are implanted onto nude mice. Patches with alternating high and low growth become particularly prominent in the large tumor-like organoids grown from monodispersed cells in nude mice. The pattern much reminds of similar observations in growing intact thyroids. Since there is no significant correlation between the fraction of [3H]thymidine labeled cells and the size of two- or three-dimensional clusters in any experiment, growth of signal-spreading cells is assumed to occur in leaps and bounds. Growth velocity in each subclone of a cell population depends on the mean interval between bursts of replications and on the number of cells synchronized by cell-to-cell diffusion of the growth signal emanating from one dividing cell. Thus, growth-promoting and growth-inhibiting factors may not only act on the mean interval between successive growth bursts, but they may also change cell-to-cell spreading of growth signals.
Authors:
M Derwahl; H Studer; G Huber; H Gerber; H J Peter
Related Documents :
11278744 - The p38 mapk pathway is required for cell growth inhibition of human breast cancer cell...
2759344 - Are continuous cell lines safe as substrates for human drugs and biologics? a case stud...
21696184 - Non-invasive transdermal iontophoretic delivery of biologically active human basic fibr...
9139874 - Invasion of human colorectal carcinoma cells is promoted by endogenous basic fibroblast...
7927934 - Spatial distribution of mitosis, apoptosis and small blood vessels in malignant diffuse...
9811004 - Early cellular response in tendon injury: the effect of loading.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Endocrinology     Volume:  127     ISSN:  0013-7227     ISO Abbreviation:  Endocrinology     Publication Date:  1990 Nov 
Date Detail:
Created Date:  1990-12-04     Completed Date:  1990-12-04     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  2104-10     Citation Subset:  AIM; IM    
Affiliation:
Laboratory of Endocrinology, University Clinic of Internal Medicine, Inselspital, Berne, Switzerland.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Autoradiography
Cell Aggregation
Cell Division
Goiter / pathology
Growth Substances / physiology*
Humans
Thymidine / metabolism
Thyroid Gland / cytology*,  metabolism
Time Factors
Tritium / diagnostic use
Chemical
Reg. No./Substance:
0/Growth Substances; 10028-17-8/Tritium; 50-89-5/Thymidine

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


Previous Document:  Monoclonal antibodies against luteinizing hormone receptor. Immunochemical characterization of the r...
Next Document:  Expression of the pregnancy-specific beta 1-glycoprotein gene in cultured human trophoblasts.