Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state

نویسندگان

  • Anna Leonov
  • Rachel Feldman
  • Amanda Piano
  • Anthony Arlia-Ciommo
  • Vicky Lutchman
  • Masoumeh Ahmadi
  • Sarah Elsaser
  • Hana Fakim
  • Mahdi Heshmati-Moghaddam
  • Asimah Hussain
  • Sandra Orfali
  • Harshvardhan Rajen
  • Negar Roofigari-Esfahani
  • Leana Rosanelli
  • Vladimir I. Titorenko
چکیده

A yeast culture grown in a nutrient-rich medium initially containing 2% glucose is not limited in calorie supply. When yeast cells cultured in this medium consume glucose, they undergo cell cycle arrest at a checkpoint in late G1 and differentiate into quiescent and non-quiescent cell populations. Studies of such differentiation have provided insights into mechanisms of yeast chronological aging under conditions of excessive calorie intake. Caloric restriction is an aging-delaying dietary intervention. Here, we assessed how caloric restriction influences the differentiation of chronologically aging yeast cultures into quiescent and non-quiescent cells, and how it affects their properties. We found that caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of quiescence, entry into a non-quiescent state and survival in this state. Our findings suggest that caloric restriction delays yeast chronological aging by causing specific changes in the following: 1) a checkpoint in G1 for cell cycle arrest and entry into a quiescent state; 2) a growth phase in which high-density quiescent cells are committed to become low-density quiescent cells; 3) the differentiation of low-density quiescent cells into low-density non-quiescent cells; and 4) the conversion of high-density quiescent cells into high-density non-quiescent cells.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2017