The gp130 Cytokines Interleukin-11 and Ciliary Neurotropic Factor Regulate through Specific Receptors the Function and Growth of Lactosomatotropic and Folliculostellate Pituitary Cell Lines1
Two of the most potent cytokines regulating anterior pituitary cell function are leukemia inhibitory factor and interleukin-6 (IL-6), which belong to the cytokine receptor family using the common gp130 signal transducer. We studied the actions of two other members of this family, IL-11 and ciliary n...
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Published in | Endocrinology (Philadelphia) Vol. 141; no. 5; pp. 1746 - 1753 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Endocrine Society
01.05.2000
|
Online Access | Get full text |
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Summary: | Two of the most potent cytokines regulating anterior pituitary cell
function are leukemia inhibitory factor and interleukin-6 (IL-6), which
belong to the cytokine receptor family using the common gp130 signal
transducer. We studied the actions of two other members of this family,
IL-11 and ciliary neurotropic factor (CNTF), on folliculostellate (FS)
cells (TtT/GF cell line) and lactosomatotropic cells (GH3 cell line).
The messenger RNA (mRNA) for the α-chain specific for the IL-11
receptor (1.7 kb) and CNTF receptor (2 kb) are expressed on both cell
types. In addition, we detected CNTF receptor mRNA in normal rat
anterior pituitary cells. IL-11 (1.25–5 nm) dose
dependently stimulated the proliferation of FS cells. CNTF, at doses
from 0.4–2 nm, also significantly stimulated the growth of
these cells. In addition, both cytokines significantly stimulated
proliferation of lactosomatotropic GH3 cells, and CNTF stimulated
hormone production (GH and PRL) at 24 h by these cells. At 16–72
h, IL-11 stimulates the secretion of the angiogenic factor vascular
endothelial growth factor by FS cells. In addition, both GH3 and FS
cells express CNTF mRNA. These data suggest that IL-11 and CNTF may act
as growth and regulatory factors in anterior pituitary cells. |
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ISSN: | 0013-7227 1945-7170 |
DOI: | 10.1210/endo.141.5.7442 |