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Article Addendum
Regulation of cell growth by autophagy
Tibor Vellai, Bertalan Bicsák, Márton L. Tóth, Krisztina Takács-Vellai and Attila L. Kovács
volume 4 | issue 4
16 May 2008Pages: 507 - 509
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Cell growththe primary determinant of cell sizehas an intimate relationship with proliferation; cells divide only after they reach a critical size. Despite its developmental and medical significance, little is known about cellular pathways that mediate the growth of cells. Accumulating evidence demonstrates a role for autophagya mechanism of eukaryotic cells to digest their own constituents during development or starvationin cell size control. Increasing autophagic activity by prolonged starvation, rapamycin treatment inhibiting TOR (target of rapamycin) signaling, or genetic intervention, causes cellular atrophy in worms, flies and mammalian cell cultures. In contrast, we have shown that in the nematode Caenorhabditis elegans mutational inactivation of two autophagy genes, unc-51/Atg1 and bec-1/Atg6, confers reduced cell size. We argue that physiological levels of autophagy are required for normal cell size, whereas both insufficient and excessive levels of autophagy lead to retarded cell growth. Furthermore, we discuss data suggesting that the insulin/IGF-1 (insulin-like growth factor receptor-1) and TGFβ (transforming growth factor-beta) signaling systems acting as major growth regulatory pathways converge on autophagy genes to control cell size. Thus, autophagy may act as a central regulatory mechanism of cell growth.
Addendum to: Aladzsity I, Tóth ML, Sigmond T, Szabó E., Bicsák B, Barna J, Regős A, Orosz L, Kovács AL, Vellai T. Autophagy genes unc-51 and bec-1 are required for normal cell size in Caenorhabditis elegans. Genetics 2007; 177:655-60, DOI: 10.1534/genetics.107.075762
Authors
Tibor Vellai
Eötvös Loránd University
Bertalan Bicsák
Eötvös Loránd University
Márton L. Tóth
ELTE University
Krisztina Takács-Vellai
Eötvös Loránd University
Attila L. Kovács
Eötvös Loránd University





