New Roles of the Primary Cilium in Autophagy

被引:22
作者
Avalos, Yenniffer [1 ]
Pena-Oyarzun, Daniel [2 ,3 ,4 ]
Budini, Mauricio [5 ]
Morselli, Eugenia [1 ]
Criollo, Alfredo [2 ,3 ,5 ]
机构
[1] Pontificia Univ Catolica Chile, Dept Fisiol, Fac Ciencias Biol, Santiago 7820436, Chile
[2] Adv Ctr Chron Dis ACCDiS, Fac Ciencias Quim & Farmaceut, Santiago 8380494, Chile
[3] Adv Ctr Chron Dis ACCDiS, Fac Med, Santiago 8380494, Chile
[4] Ctr Mol Studies Cell CEMC, Fac Med, Santiago 8380453, Chile
[5] Inst Invest Ciencias Odontol ICOD, Fac Odontol, Santiago 8380492, Chile
关键词
POLYCYSTIC KIDNEY-DISEASE; BARDET-BIEDL SYNDROME; SYNDROME PROTEINS; INSULIN SENSITIVITY; GLUCOSE-METABOLISM; LEPTIN RESISTANCE; MOUSE MODELS; CELL-SIZE; OBESITY; INTRAFLAGELLAR;
D O I
10.1155/2017/4367019
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The primary cilium is a nonmotile organelle that emanates from the surface of multiple cell types and receives signals from the environment to regulate intracellular signaling pathways. The presence of cilia, as well as their length, is important for proper cell function; shortened, elongated, or absent cilia are associated with pathological conditions. Interestingly, it has recently been shown that the molecular machinery involved in autophagy, the process of recycling of intracellular material to maintain cellular and tissue homeostasis, participates in ciliogenesis. Cilium-dependent signaling is necessary for autophagosome formation and, conversely, autophagy regulates both ciliogenesis and cilium length by degrading specific ciliary proteins. Here, we will discuss the relationship that exists between the two processes at the cellular and molecular level, highlighting what is known about the effects of ciliary dysfunction in the control of energy homeostasis in some ciliopathies.
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页数:16
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