Document Detail


Analysis of homogeneous populations of anterior pituitary folliculostellate cells by laser capture microdissection and reverse transcription-polymerase chain reaction.
MedLine Citation:
PMID:  11316732     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Pituitary folliculostellate (FS) cells are usually located between the secretory cells in the anterior pituitary, and they produce many peptides that exert a paracrine effect on hormone-producing pituitary cells. Previous approaches have been unsuccessful in obtaining homogeneous populations of FS cells. We used a combination of immunostaining with S100 protein followed by laser capture microdissection (Immuno-LCM) to obtain purified populations of rat FS cells. These cells were analyzed along with a mouse FS cell line (TtT/GF) by RT-PCR for gene expression. RT-PCR analyses showed that both FS cell populations expressed the mRNAs for glial fibrillary acidic protein, S100 protein, transforming growth factor-beta1 (TGFbeta1), TGFbeta receptor, interleukin-6, leptin, leptin receptor, pituitary adenylate cyclase-activating polypeptide (PACAP), and PACAP receptors. Both FS cell populations were negative for PRL, GH, and POMC, supporting the homogeneity of the rat FS cell population. TGFbeta1, but not PACAP-38, treatment stimulated cell proliferation in both FS cell populations. TGFbeta1 increased leptin, but not interleukin-6, mRNA expression in rat FS cells. However, TGFbeta1 inhibited leptin RNA expression in the TtT/GF cell line, as shown by RT-PCR and Northern blot analysis. These results indicate that 1) homogeneous populations of FS cells can be prepared by Immuno-LCM; 2) TGFbeta1 stimulates the proliferation of normal rat FS cells and the TtT/GF cell line; and 3) the effects of TGFbeta1 to stimulate leptin mRNA expression in rat FS cells but inhibit leptin mRNA expression in TtT/GF cells probably reflect alterations in signal transduction in the TtT/GF cell line.
Authors:
L Jin; I Tsumanuma; K H Ruebel; J M Bayliss; R V Lloyd
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Endocrinology     Volume:  142     ISSN:  0013-7227     ISO Abbreviation:  Endocrinology     Publication Date:  2001 May 
Date Detail:
Created Date:  2001-04-24     Completed Date:  2001-05-17     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1703-9     Citation Subset:  AIM; IM    
Affiliation:
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Cell Division / drug effects
Cells, Cultured
Dissection
Female
Immunohistochemistry
Lasers
Leptin / genetics
Neuropeptides / pharmacology
Pituitary Adenylate Cyclase-Activating Polypeptide
Pituitary Gland, Anterior / cytology*
RNA, Messenger / analysis
Rats
Rats, Inbred WF
Reverse Transcriptase Polymerase Chain Reaction*
S100 Proteins / analysis
Transforming Growth Factor beta / pharmacology
Grant Support
ID/Acronym/Agency:
CA-37231/CA/NCI NIH HHS; CA-90249/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Adcyap1 protein, rat; 0/Leptin; 0/Neuropeptides; 0/Pituitary Adenylate Cyclase-Activating Polypeptide; 0/RNA, Messenger; 0/S100 Proteins; 0/Transforming Growth Factor beta

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


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