Decreased proliferation of aged rat beta cells corresponds with enhanced expression of the cell cycle inhibitor p27 KIP1

2021 ◽  
Author(s):  
Talon J. Aitken ◽  
Jacqueline E. Crabtree ◽  
Daelin M. Jensen ◽  
Kavan H. Hess ◽  
Brennan R. Leininger ◽  
...  
Pneumologie ◽  
2014 ◽  
Vol 68 (06) ◽  
Author(s):  
T Lüdtke ◽  
H Farin ◽  
C Rudat ◽  
K Schuster-Gossler ◽  
M Petry ◽  
...  

Endocrinology ◽  
2009 ◽  
Vol 150 (2) ◽  
pp. 929-935 ◽  
Author(s):  
Pradeep P. Kayampilly ◽  
K. M. J. Menon

FSH, acting through multiple signaling pathways, regulates the proliferation and growth of granulosa cells, which are critical for ovulation. The present study investigated whether AMP-activated protein kinase (AMPK), which controls the energy balance of the cell, plays a role in FSH-mediated increase in granulosa cell proliferation. Cells isolated from immature rat ovaries were grown in serum-free, phenol red free DMEM-F12 and were treated with FSH (50 ng/ml) for 0, 5, and 15 min. Western blot analysis showed a significant reduction in AMPK activation as observed by a reduction of phosphorylation at thr 172 in response to FSH treatment at all time points tested. FSH also reduced AMPK phosphorylation in a dose-dependent manner with maximum inhibition at 100 ng/ml. The chemical activator of AMPK (5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside, 0.5 mm) increased the cell cycle inhibitor p27 kip expression significantly, whereas the AMPK inhibitor (compound C, 20 μm) and FSH reduced p27kip expression significantly compared with control. FSH treatment resulted in an increase in the phosphorylation of AMPK at ser 485/491 and a reduction in thr 172 phosphorylation. Inhibition of Akt phosphorylation using Akt inhibitor VIII reversed the inhibitory effect of FSH on thr 172 phosphorylation of AMPK, whereas ERK inhibitor U0126 had no effect. These results show that FSH, through an Akt-dependent pathway, phosphorylates AMPK at ser 481/495 and inhibits its activation by reducing thr 172 phosphorylation. AMPK activation by 5-amino-imidazole-4-carboxamide-1-β-d-ribofuranoside treatment resulted in a reduction of cell cycle regulatory protein cyclin D2 mRNA expression, whereas FSH increased the expression by 2-fold. These results suggest that FSH promotes granulosa cell proliferation by increasing cyclin D2 mRNA expression and by reducing p27 kip expression by inhibiting AMPK activation through an Akt-dependent pathway. FSH stimulates granulosa cell proliferation by reducing cell cycle inhibitor p27 kip through AMP kinase inhibition.


1997 ◽  
Vol 38 (24) ◽  
pp. 4327-4328 ◽  
Author(s):  
Haishan Wang ◽  
Arasu Ganesan

2010 ◽  
Vol 23 (2) ◽  
pp. 238-251 ◽  
Author(s):  
Blanka Šestáková ◽  
Lubica Ondrušová ◽  
Jiri Vachtenheim

2006 ◽  
Vol 42 (12) ◽  
pp. 1875-1880 ◽  
Author(s):  
I. Duran ◽  
L.L. Siu ◽  
A.M. Oza ◽  
T.-B. Chung ◽  
J. Sturgeon ◽  
...  

2007 ◽  
Vol 21 (11) ◽  
pp. 2807-2817 ◽  
Author(s):  
Dana Egozi ◽  
Maanit Shapira ◽  
Galit Paor ◽  
Ofer Ben‐Izhak ◽  
Karl Skorecki ◽  
...  

2004 ◽  
Vol 13 (3) ◽  
pp. 116
Author(s):  
Manfred Boehm ◽  
Andrea C True ◽  
Michelle Olive ◽  
Martin F Crook ◽  
Hong San ◽  
...  

2018 ◽  
Author(s):  
Evgeny Zatulovskiy ◽  
Daniel F. Berenson ◽  
Benjamin R. Topacio ◽  
Jan M. Skotheim

Cell size is fundamental to function in different cell types across the human body because it sets the scale of organelle structures, biosynthesis, and surface transport1,2. Tiny erythrocytes squeeze through capillaries to transport oxygen, while the million-fold larger oocyte divides without growth to form the ~100 cell pre-implantation embryo. Despite the vast size range across cell types, cells of a given type are typically uniform in size likely because cells are able to accurately couple cell growth to division3–6. While some genes whose disruption in mammalian cells affects cell size have been identified, the molecular mechanisms through which cell growth drives cell division have remained elusive7–12. Here, we show that cell growth acts to dilute the cell cycle inhibitor Rb to drive cell cycle progression from G1 to S phase in human cells. In contrast, other G1/S regulators remained at nearly constant concentration. Rb is a stable protein that is synthesized during S and G2 phases in an amount that is independent of cell size. Equal partitioning to daughter cells of chromatin bound Rb then ensures that all cells at birth inherit a similar amount of Rb protein. RB overexpression increased cell size in tissue culture and a mouse cancer model, while RB deletion decreased cell size and removed the inverse correlation between cell size at birth and the duration of G1 phase. Thus, Rb-dilution by cell growth in G1 provides a long-sought cell autonomous molecular mechanism for cell size homeostasis.


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