Document Detail

Contact-dependent intercellular communication of bovine luteal cells in culture.
MedLine Citation:
PMID:  1935805     Owner:  NLM     Status:  MEDLINE    
Mammalian gap junctions permit exchange of nutrients, ions, and regulatory molecules of less than 1.5 kDa among contacting communication-competent cells and may be important for regulation of luteal function and maintenance of luteal homeostasis. The present studies were designed to evaluate gap junction-mediated intercellular communication between bovine luteal cells in culture. Using a dye-coupling technique along with interactive laser cytometry, selected luteal cells were studied for the rate of contact-dependent fluorescence redistribution after photobleaching. The rate of communication, reported as the rate of fluorescence recovery (percentage per min), was determined for steroidogenic cells as follows: 1) small luteal cells contacting only small luteal cells, 2) large luteal cells contacting only small luteal cells, and 3) large luteal cells contacting only large luteal cells. In addition, the effects of known regulators of luteal function [LH, prostaglandin F2 alpha (PGF), and forskolin] on the rate of intercellular communication were determined. Small luteal cells communicated rapidly with each other, exhibiting an initial rate of fluorescence recovery of 4.1 +/- 0.1%/min (n = 187). The rate of small cell-small cell communication was unaffected by LH and PGF. For large luteal cells contacting small luteal cells, however, LH and PGF stimulated (P less than 0.02) the rate of communication compared with no hormone [1.6 +/- 0.2 (n = 18) and 1.5 +/- 0.6 (n = 20) vs. 0.8 +/- 0.3%/min (n = 27), respectively]. LH and PGF in combination, however, did not enhance the rate (0.6 +/- 0.2%/min; n = 19) of large cell-small cell communication. In contrast, forskolin significantly stimulated both small cell-small cell and large cell-small cell communication rates compared with no forskolin [34% increase (n = 48) and 50% increase (n = 23), respectively]. Large luteal cells did not communicate with each other under any condition tested. Transmission electron microscopy revealed the presence of numerous gap junction-like structures in bovine luteal cells in culture. These data suggest that luteal cells are capable of intercellular communication and that the rate of communication may be influenced by hormones. Contact-dependent intercellular communication among luteal cells may, therefore, play a significant role in the regulation of luteal function.
D A Redmer; A T Grazul-Bilska; L P Reynolds
Related Documents :
25319825 - Arid3a is essential to execution of the first cell fate decision via direct embryonic a...
6309265 - Frequency-dependent coupling between rhythmically active neurons in the leech.
2953845 - The specific direct interaction of helper t cells and antigen-presenting b cells. ii. r...
6715265 - Gap junctions in the stria vascularis and effects of ethacrynic acid.
16931585 - Defining ploidy-specific thresholds in array comparative genomic hybridization to impro...
19482835 - Induction of human alveolar epithelial cell growth factor receptors by dendrimeric nano...
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Endocrinology     Volume:  129     ISSN:  0013-7227     ISO Abbreviation:  Endocrinology     Publication Date:  1991 Nov 
Date Detail:
Created Date:  1991-12-02     Completed Date:  1991-12-02     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  2757-66     Citation Subset:  AIM; IM    
Department of Animal and Range Sciences, North Dakota State University, Fargo 58105.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Cell Communication / physiology*
Cells, Cultured
Corpus Luteum / cytology*,  metabolism,  ultrastructure
Dinoprost / pharmacology
Forskolin / pharmacology
Intercellular Junctions / physiology*
Luteinizing Hormone / pharmacology
Microscopy, Electron
Progesterone / metabolism
Tamoxifen / pharmacology
Reg. No./Substance:
10540-29-1/Tamoxifen; 551-11-1/Dinoprost; 57-83-0/Progesterone; 66428-89-5/Forskolin; 9002-67-9/Luteinizing Hormone

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

Previous Document:  Molecular cloning and expression of rat placental lactogen-Iv, a variant of rPL-I present in late pr...
Next Document:  Triiodothyronine receptor beta-2 messenger ribonucleic acid expression by somatotropes and thyrotrop...