Activins and inhibins are members of the TGFbeta family of growth and differentiation that were discovered by virtue of their reciprocal effects on the production of FSH. These pleiotropic proteins play a wide variety of endocrine, paracrine and autocrine roles within normal and neoplastic reproductive and other tissues. The binding of activin to its specific type II receptor serine kinase kinase (RSK) leads to the recruitment and trans- phosphorylation of its cognate type I RSK (Activin Like Kinase-4) and the subsequent phosphorylation of downstream mediators, the pathway- specific Smads.
Under Aim I, we will examine the nature of the interactions between the components of activin signaling. Based on the elucidation of the structure of the ligand binding domain of the type II activin receptor by Project III, we are expressing a series of mutant receptors in mammalian cells and analyzing their affinities for activin, inhibin and the type I receptor (ALK4). These efforts are highly complementary to Choe (Project III), who is working to solve the structure of the ActRII/activin/ALK4 complex and to Fischer (Project IV) who is mutating activin itself..
The second Aim i nvolves the study of mechanisms that serve to limit the biological effects of activin itself. We have observed cellular desensitization of the transcriptional response to activin and will explore mechanisms, including the possibility that this is mediated by the inhibitory Smad, Smad7. We will continue to explore the mode of action of inhibin; this will include a continued effort to clone an inhibin specific binding component. If we are successful, a series of biochemical and cellular experiments will ensure to determine the importance of this protein. If warranted, we will generate and analyze mice deficient in the inhibin receptor.
Under Aim III we will continue to explore paracrine and autocrine mechanisms within the pituitary, examining the interesting possibility that some cytokine effects may be mediated through increased production of follistatin. The roles and regulation of Smad7 in the pituitary and gonadotropes, will be explored by a variety of approaches, including the generation of Smad 7 null mice, in which, Smad7 is conditionally knocked out in gonadotropes. This intra-pituitary modulatory network provides a mechanism for the integration of central and peripheral inputs and may be critical for the differential production of FSH and LH under defined physiological circumstances. Drugs and other approaches targeting components of the extracellular and intracellular activin signaling system may prove to be useful for the management of human fertility and reproductive disorders.

Project Start
2001-04-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
22
Fiscal Year
2001
Total Cost
$197,421
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
005436803
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Muenster, Uwe; Korupolu, Radhika; Rastogi, Ratindra et al. (2011) Antagonism of activin by activin chimeras. Vitam Horm 85:105-28
Kim, Meejung; Choe, Senyon (2011) BMPs and their clinical potentials. BMB Rep 44:619-34
Looyenga, Brendan D; Wiater, Ezra; Vale, Wylie et al. (2010) Inhibin-A antagonizes TGFbeta2 signaling by down-regulating cell surface expression of the TGFbeta coreceptor betaglycan. Mol Endocrinol 24:608-20
Valera, Elvira; Isaacs, Michael J; Kawakami, Yasuhiko et al. (2010) BMP-2/6 heterodimer is more effective than BMP-2 or BMP-6 homodimers as inductor of differentiation of human embryonic stem cells. PLoS One 5:e11167
Isaacs, Michael J; Kawakami, Yasuhiko; Allendorph, George P et al. (2010) Bone morphogenetic protein-2 and -6 heterodimer illustrates the nature of ligand-receptor assembly. Mol Endocrinol 24:1469-77
Hassold, Terry; Hunt, Patricia (2009) Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew. Curr Opin Pediatr 21:703-8
Wiater, Ezra; Lewis, Kathy A; Donaldson, Cynthia et al. (2009) Endogenous betaglycan is essential for high-potency inhibin antagonism in gonadotropes. Mol Endocrinol 23:1033-42
Cheng, Edith Y; Hunt, Patricia A; Naluai-Cecchini, Theresa A et al. (2009) Meiotic recombination in human oocytes. PLoS Genet 5:e1000661
Ciarmela, Pasquapina; Wiater, Ezra; Smith, Sean M et al. (2009) Presence, actions, and regulation of myostatin in rat uterus and myometrial cells. Endocrinology 150:906-14
Blount, Amy L; Vaughan, Joan M; Vale, Wylie W et al. (2008) A Smad-binding element in intron 1 participates in activin-dependent regulation of the follistatin gene. J Biol Chem 283:7016-26

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