TOR complex 2 (TORC2) in Dictyostelium suppresses phagocytic nutrient capture independently of TORC1-mediated nutrient sensing.
J Cell Sci
; 125(Pt 1): 37-48, 2012 Jan 01.
Article
em En
| MEDLINE
| ID: mdl-22266904
ABSTRACT
The TOR protein kinase functions in two distinct complexes, TOR complex 1 (TORC1) and 2 (TORC2). TORC1 is required for growth in response to growth factors, nutrients and the cellular energy state; TORC2 regulates AKT signaling, which can modulate cytoskeletal polarization. In its ecological niche, Dictyostelium engulf bacteria and yeast for nutrient capture. Despite the essential role of TORC1 in control of cellular growth, we show that nutrient particle capture (phagocytosis) in Dictyostelium is independent of TORC1-mediated nutrient sensing and growth regulation. However, loss of Dictyostelium TORC2 components Rictor/Pia, SIN1/RIP3 and Lst8 promotes nutrient particle uptake; inactivation of TORC2 leads to increased efficiency and speed of phagocytosis. In contrast to phagocytosis, we show that macropinocytosis, an AKT-dependent process for cellular uptake of fluid phase nutrients, is not regulated by either of the TOR complexes. The integrated and balanced regulation of TORC1 and TORC2 might be crucial in Dictyostelium to coordinate growth and energy needs with other essential TOR-regulated processes.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Fagocitose
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Complexos Multiproteicos
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Dictyostelium
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Serina-Treonina Quinases TOR
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Alimentos
Limite:
Animals
Idioma:
En
Revista:
J Cell Sci
Ano de publicação:
2012
Tipo de documento:
Article
País de afiliação:
Estados Unidos