p53 Plays a Role in Mesenchymal Differentiation Programs, in a Cell Fate Dependent Manner

被引:149
作者
Molchadsky, Alina [1 ]
Shats, Igor [1 ]
Goldfinger, Naomi [1 ]
Pevsner-Fischer, Meirav [1 ]
Olson, Melissa [2 ]
Rinon, Ariel [3 ]
Tzahor, Eldad [3 ]
Lozano, Guillermina [2 ]
Zipori, Dov [1 ]
Sarig, Rachel [1 ]
Rotter, Varda [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Univ Texas, MD Anderson Canc Ctr, Dept Canc Genet, Houston, TX USA
[3] Weizmann Inst Sci, Dept Biol Regulat, Rehovot, Israel
来源
PLOS ONE | 2008年 / 3卷 / 11期
关键词
D O I
10.1371/journal.pone.0003707
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The tumor suppressor p53 is an important regulator that controls various cellular networks, including cell differentiation. Interestingly, some studies suggest that p53 facilitates cell differentiation, whereas others claim that it suppresses differentiation. Therefore, it is critical to evaluate whether this inconsistency represents an authentic differential p53 activity manifested in the various differentiation programs. Methodology/Principal Findings: To clarify this important issue, we conducted a comparative study of several mesenchymal differentiation programs. The effects of p53 knockdown or enhanced activity were analyzed in mouse and human mesenchymal cells, representing various stages of several differentiation programs. We found that p53 down-regulated the expression of master differentiation-inducing transcription factors, thereby inhibiting osteogenic, adipogenic and smooth muscle differentiation of multiple mesenchymal cell types. In contrast, p53 is essential for skeletal muscle differentiation and osteogenic re-programming of skeletal muscle committed cells. Conclusions: These comparative studies suggest that, depending on the specific cell type and the specific differentiation program, p53 may exert a positive or a negative effect, and thus can be referred as a "guardian of differentiation'' at large.
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页数:15
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