Literature DB >> 20032047

The follistatin-288 isoform alone is sufficient for survival but not for normal fertility in mice.

Fuminori Kimura1, Yisrael Sidis, Lara Bonomi, Yin Xia, Alan Schneyer.   

Abstract

Follistatin (FST) is a natural antagonist of activin and related TGFbeta superfamily ligands that exists as three protein isoforms differing in length at the C terminus. The longest FST315 isoform is found in the circulation, whereas the shortest FST288 isoform is typically found in or on cells and tissues, and the intermediate FST303 isoform is found in gonads. We recently demonstrated that the FST isoforms have distinct biological actions in vitro that, taken together with the differential distribution, suggests they may also have different roles in vivo. To explore the specific role of individual FST isoforms, we created a single-isoform FST288-only mouse. In contrast to the neonatal death of FST global knockout mice, FST288-only mice survive to adulthood. Although they appear normal, FST288-only mice have fertility defects including reduced litter size and frequency. Follicles were counted in ovaries from 8.5- to 400-d-old females. Significantly fewer morphologically healthy antral follicles were found in 100- to 250-d FST288-only ovaries, but there were significantly more secondary, primary, and primordial follicles detected at d 8.5 in FST288-only ovaries. However, depletion of this primordial follicle pool is more rapid in FST288-only females resulting in a deficit by 250 d of age and early cessation of reproduction. Superovulated FST288-only females have fewer ovulated eggs and embryos. These results indicate that the FST isoforms have different activities in vivo, that the FST288-only isoform is sufficient for development, and that loss of FST303 and FST315 isoforms results in fertility defects that resemble activin hyperactivity and premature ovarian failure.

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Year:  2009        PMID: 20032047      PMCID: PMC2840692          DOI: 10.1210/en.2009-1176

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  28 in total

1.  Differential biosynthesis and intracellular transport of follistatin isoforms and follistatin-like-3.

Authors:  Seiichiro Saito; Yisrael Sidis; Abir Mukherjee; Yin Xia; Alan Schneyer
Journal:  Endocrinology       Date:  2005-09-08       Impact factor: 4.736

2.  Postnatal regulation of germ cells by activin: the establishment of the initial follicle pool.

Authors:  Sarah K Bristol-Gould; Pamela K Kreeger; Christina G Selkirk; Signe M Kilen; Robert W Cook; Jingjing L Kipp; Lonnie D Shea; Kelly E Mayo; Teresa K Woodruff
Journal:  Dev Biol       Date:  2006-06-17       Impact factor: 3.582

3.  Biological activity of follistatin isoforms and follistatin-like-3 is dependent on differential cell surface binding and specificity for activin, myostatin, and bone morphogenetic proteins.

Authors:  Yisrael Sidis; Abir Mukherjee; Henry Keutmann; Anne Delbaere; Miyuki Sadatsuki; Alan Schneyer
Journal:  Endocrinology       Date:  2006-04-20       Impact factor: 4.736

4.  Pituitary follistatin regulates activin-mediated production of follicle-stimulating hormone during the rat estrous cycle.

Authors:  L M Besecke; M J Guendner; P A Sluss; A G Polak; T K Woodruff; J L Jameson; A C Bauer-Dantoin; J Weiss
Journal:  Endocrinology       Date:  1997-07       Impact factor: 4.736

Review 5.  Biological bases of premature ovarian failure.

Authors:  R G Gosden; M J Faddy
Journal:  Reprod Fertil Dev       Date:  1998       Impact factor: 2.311

6.  A model conforming the decline in follicle numbers to the age of menopause in women.

Authors:  M J Faddy; R G Gosden
Journal:  Hum Reprod       Date:  1996-07       Impact factor: 6.918

Review 7.  Regulation of primordial follicle assembly and development.

Authors:  Michael K Skinner
Journal:  Hum Reprod Update       Date:  2005-07-08       Impact factor: 15.610

8.  Fate of the initial follicle pool: empirical and mathematical evidence supporting its sufficiency for adult fertility.

Authors:  Sarah K Bristol-Gould; Pamela K Kreeger; Christina G Selkirk; Signe M Kilen; Kelly E Mayo; Lonnie D Shea; Teresa K Woodruff
Journal:  Dev Biol       Date:  2006-06-18       Impact factor: 3.582

9.  Kit-ligand/stem cell factor induces primordial follicle development and initiates folliculogenesis.

Authors:  J A Parrott; M K Skinner
Journal:  Endocrinology       Date:  1999-09       Impact factor: 4.736

10.  Multiple defects and perinatal death in mice deficient in follistatin.

Authors:  M M Matzuk; N Lu; H Vogel; K Sellheyer; D R Roop; A Bradley
Journal:  Nature       Date:  1995-03-23       Impact factor: 49.962

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  15 in total

1.  Activin B regulates islet composition and islet mass but not whole body glucose homeostasis or insulin sensitivity.

Authors:  Lara Bonomi; Melissa Brown; Nathan Ungerleider; Meghan Muse; Martin M Matzuk; Alan Schneyer
Journal:  Am J Physiol Endocrinol Metab       Date:  2012-06-26       Impact factor: 4.310

Review 2.  Inhibin at 90: from discovery to clinical application, a historical review.

Authors:  Yogeshwar Makanji; Jie Zhu; Rama Mishra; Chris Holmquist; Winifred P S Wong; Neena B Schwartz; Kelly E Mayo; Teresa K Woodruff
Journal:  Endocr Rev       Date:  2014-07-22       Impact factor: 19.871

Review 3.  Activins and Inhibins: Roles in Development, Physiology, and Disease.

Authors:  Maria Namwanje; Chester W Brown
Journal:  Cold Spring Harb Perspect Biol       Date:  2016-07-01       Impact factor: 10.005

4.  The Local Control of the Pituitary by Activin Signaling and Modulation.

Authors:  Louise M Bilezikjian; Wylie W Vale
Journal:  Open Neuroendocrinol J       Date:  2011-01-01

5.  Differential synthesis and action of TGFß superfamily ligands in mouse and rat islets.

Authors:  Melissa L Brown; Fuminori Kimura; Lara M Bonomi; Nathan A Ungerleider; Alan L Schneyer
Journal:  Islets       Date:  2011-11-01       Impact factor: 2.694

6.  Follistatin is critical for mouse uterine receptivity and decidualization.

Authors:  Paul T Fullerton; Diana Monsivais; Ramakrishna Kommagani; Martin M Matzuk
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-30       Impact factor: 11.205

Review 7.  Cell-type specific modulation of pituitary cells by activin, inhibin and follistatin.

Authors:  Louise M Bilezikjian; Nicholas J Justice; Alissa N Blackler; Ezra Wiater; Wylie W Vale
Journal:  Mol Cell Endocrinol       Date:  2012-02-04       Impact factor: 4.102

8.  A non-coding region near Follistatin controls head colour polymorphism in the Gouldian finch.

Authors:  Matthew B Toomey; Cristiana I Marques; Pedro Andrade; Pedro M Araújo; Stephen Sabatino; Małgorzata A Gazda; Sandra Afonso; Ricardo J Lopes; Joseph C Corbo; Miguel Carneiro
Journal:  Proc Biol Sci       Date:  2018-10-03       Impact factor: 5.349

Review 9.  Regulation of the ovarian reserve by members of the transforming growth factor beta family.

Authors:  Stephanie A Pangas
Journal:  Mol Reprod Dev       Date:  2012-09-11       Impact factor: 2.609

10.  Increased activin bioavailability enhances hepatic insulin sensitivity while inducing hepatic steatosis in male mice.

Authors:  Nathan A Ungerleider; Lara M Bonomi; Melissa L Brown; Alan L Schneyer
Journal:  Endocrinology       Date:  2013-03-26       Impact factor: 4.736

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