Role of Liquid-Liquid Separation in Endocrine and Living Cells.

cellular body paraspeckle phase transition sex development type 2 diabetes

Journal

Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997

Informations de publication

Date de publication:
01 Oct 2021
Historique:
received: 23 03 2021
entrez: 16 8 2021
pubmed: 17 8 2021
medline: 17 8 2021
Statut: epublish

Résumé

Recent studies have revealed that every eukaryotic cell contains several membraneless organelles created via liquid-liquid phase separation (LLPS). LLPS is a physical phenomenon that transiently compartmentalizes the subcellular space and thereby facilitates various biological reactions. LLPS is indispensable for cellular functions; however, dysregulated LLPS has the potential to cause irreversible protein aggregation leading to degenerative disorders. To date, there is no systematic review on the role of LLPS in endocrinology. We explored previous studies which addressed roles of LLPS in living cells, particularly from the viewpoint of endocrinology. To this end, we screened relevant literature in PubMed published between 2009 and 2021 using LLPS-associated keywords including "membraneless organelle," "phase transition," and "intrinsically disordered," and endocrinological keywords such as "hormone," "ovary," "androgen," and "diabetes." We also referred to the articles in the reference lists of identified papers. Based on 67 articles selected from 449 papers, we provided a concise overview of the current understanding of LLPS in living cells. Then, we summarized recent articles documenting the physiological or pathological roles of LLPS in endocrine cells. The discovery of LLPS in cells has resulted in a paradigm shift in molecular biology. Recent studies indicate that LLPS contributes to male sex development by providing a functional platform for SOX9 and CBX2 in testicular cells. In addition, dysregulated LLPS has been implicated in aberrant protein aggregation in pancreatic β-cells, leading to type 2 diabetes. Still, we are just beginning to understand the significance of LLPS in endocrine cells.

Identifiants

pubmed: 34396024
doi: 10.1210/jendso/bvab126
pii: bvab126
pmc: PMC8358989
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

bvab126

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society.

Références

Proc Natl Acad Sci U S A. 2020 Jun 2;117(22):12050-12061
pubmed: 32414928
J Theor Biol. 2017 Dec 7;434:42-49
pubmed: 28392184
J Cell Biol. 2019 Dec 2;218(12):4127-4140
pubmed: 31636118
Cell. 2018 Apr 19;173(3):706-719.e13
pubmed: 29677514
Curr Opin Cell Biol. 2017 Jun;46:62-71
pubmed: 28343140
Genes Dev. 2019 Dec 1;33(23-24):1619-1634
pubmed: 31594803
Mol Cell Biol. 2007 Jul;27(13):4863-75
pubmed: 17452459
Genes Dev. 2019 Jul 1;33(13-14):799-813
pubmed: 31171700
Noncoding RNA. 2020 Jul 01;6(3):
pubmed: 32630183
EMBO J. 2012 Oct 17;31(20):4020-34
pubmed: 22960638
Cell. 2015 Aug 27;162(5):1066-77
pubmed: 26317470
Noncoding RNA. 2019 Nov 01;5(4):
pubmed: 31683819
Trends Biochem Sci. 2018 Feb;43(2):124-135
pubmed: 29289458
Cancer Sci. 2020 Sep;111(9):3155-3163
pubmed: 32594560
Curr Opin Cell Biol. 2020 Jun;64:67-76
pubmed: 32259767
Nature. 1991 Jul 4;352(6330):77-9
pubmed: 2062380
Front Biosci (Landmark Ed). 2012 Jan 01;17:1729-46
pubmed: 22201832
Nat Genet. 2006 Dec;38(12):1369-71
pubmed: 17086185
Dev Cell. 2013 Oct 28;27(2):161-173
pubmed: 24176641
Wiley Interdiscip Rev RNA. 2020 Jan;11(1):e1574
pubmed: 31680436
Am J Hum Genet. 2009 May;84(5):658-63
pubmed: 19361780
Nat Commun. 2015 Aug 19;6:8088
pubmed: 26286827
Science. 2018 Jul 27;361(6400):
pubmed: 29930091
J Mol Biol. 2018 Nov 2;430(23):4773-4805
pubmed: 30017918
Dev Cell. 2020 Oct 12;55(1):4-17
pubmed: 33007213
Science. 2018 May 25;360(6391):918-921
pubmed: 29650702
Cell. 2016 Sep 8;166(6):1572-1584.e16
pubmed: 27594427
Nat Rev Mol Cell Biol. 2017 May;18(5):285-298
pubmed: 28225081
Proteomics. 2018 Mar;18(5-6):e1700193
pubmed: 29068531
Endocr Dev. 2016;29:36-49
pubmed: 26680571
Semin Cancer Biol. 2016 Jun;37-38:36-50
pubmed: 26721423
Open Biol. 2018 Oct 24;8(10):
pubmed: 30355755
Phys Rev Lett. 2013 Aug 23;111(8):088101
pubmed: 24010479
J Biol Chem. 2019 Feb 1;294(5):1451-1463
pubmed: 30514760
Cell. 2020 Dec 23;183(7):1742-1756
pubmed: 33357399
Science. 2009 Jun 26;324(5935):1729-32
pubmed: 19460965
Endocrinology. 2012 Feb;153(2):913-24
pubmed: 22186409
Trends Genet. 2019 Sep;35(9):658-671
pubmed: 31288943
Mol Reprod Dev. 2020 Nov;87(11):1124-1125
pubmed: 33022123
Science. 2017 Sep 22;357(6357):
pubmed: 28935776
Curr Opin Struct Biol. 2017 Jun;44:18-30
pubmed: 27838525
Nat Struct Mol Biol. 2019 Mar;26(3):193-203
pubmed: 30833784
Int J Mol Sci. 2020 Sep 16;21(18):
pubmed: 32947964
Cell. 2019 Jan 24;176(3):419-434
pubmed: 30682370
Annu Rev Microbiol. 2018 Sep 08;72:255-271
pubmed: 30200855
J Clin Invest. 2008 Sep;118(9):3098-108
pubmed: 18677406
Science. 2020 Jan 31;367(6477):
pubmed: 32001628
Cell. 1994 Dec 16;79(6):1111-20
pubmed: 8001137
Trends Cell Biol. 2018 Jun;28(6):420-435
pubmed: 29602697
Biol Reprod. 2006 Sep;75(3):352-9
pubmed: 16641145
Curr Opin Cell Biol. 2019 Dec;61:117-125
pubmed: 31480011
Trends Cell Biol. 2016 Jul;26(7):547-558
pubmed: 27051975
Nature. 1998 Jun 18;393(6686):688-92
pubmed: 9641679
J Biol Chem. 2008 Feb 29;283(9):5525-32
pubmed: 18162467
PLoS Biol. 2013;11(6):e1001577
pubmed: 23762018
Hum Mol Genet. 2015 Sep 1;24(17):4933-47
pubmed: 26060192
Proc Natl Acad Sci U S A. 2011 Mar 15;108(11):4334-9
pubmed: 21368180
Mol Cell. 2018 Jun 21;70(6):1038-1053.e7
pubmed: 29932899
Cell. 2013 Feb 14;152(4):791-805
pubmed: 23415227
Proc Natl Acad Sci U S A. 2016 Nov 1;113(44):12473-12477
pubmed: 27791129
Nature. 1994 Dec 8;372(6506):525-30
pubmed: 7990924
J Cell Biol. 2011 Apr 4;193(1):31-9
pubmed: 21444682
Front Physiol. 2020 Dec 08;11:606889
pubmed: 33424631
Nat Struct Mol Biol. 2017 Oct;24(10):816-824
pubmed: 28846091

Auteurs

Kazuhisa Akiba (K)

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 157-8535 Tokyo, Japan.
Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, 183-8561 Tokyo, Japan.

Yuko Katoh-Fukui (Y)

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 157-8535 Tokyo, Japan.

Kei Yoshida (K)

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 157-8535 Tokyo, Japan.

Satoshi Narumi (S)

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 157-8535 Tokyo, Japan.

Mami Miyado (M)

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 157-8535 Tokyo, Japan.

Yukihiro Hasegawa (Y)

Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, 183-8561 Tokyo, Japan.

Maki Fukami (M)

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 157-8535 Tokyo, Japan.

Classifications MeSH