scholarly journals Tumor suppressive autophagy in intestinal stem cells controls gut homeostasis

Autophagy ◽  
2019 ◽  
Vol 15 (9) ◽  
pp. 1668-1670 ◽  
Author(s):  
Peng Zhang ◽  
Andreana N. Holowatyj ◽  
Cornelia M. Ulrich ◽  
Bruce A. Edgar
Cell Reports ◽  
2015 ◽  
Vol 11 (1) ◽  
pp. 33-42 ◽  
Author(s):  
Hua Tian ◽  
Brian Biehs ◽  
Cecilia Chiu ◽  
Christian W. Siebel ◽  
Yan Wu ◽  
...  

Cell Reports ◽  
2016 ◽  
Vol 15 (5) ◽  
pp. 911-918 ◽  
Author(s):  
Tomas Valenta ◽  
Bahar Degirmenci ◽  
Andreas E. Moor ◽  
Patrick Herr ◽  
Dario Zimmerli ◽  
...  

2020 ◽  
Vol 21 (17) ◽  
pp. 6362 ◽  
Author(s):  
Aurélia Joly ◽  
Raphaël Rousset

Tissues must adapt to the different external stimuli so that organisms can survive in their environments. The intestine is a vital organ involved in food processing and absorption, as well as in innate immune response. Its adaptation to environmental cues such as diet and biotic/abiotic stress involves regulation of the proliferative rate and a switch of division mode (asymmetric versus symmetric) of intestinal stem cells (ISC). In this review, we outline the current comprehension of the physiological and molecular mechanisms implicated in stem cell division modes in the adult Drosophila midgut. We present the signaling pathways and polarity cues that control the mitotic spindle orientation, which is the terminal determinant ensuring execution of the division mode. We review these events during gut homeostasis, as well as during its response to nutrient availability, bacterial infection, chemical damage, and aging. JNK signaling acts as a central player, being involved in each of these conditions as a direct regulator of spindle orientation. The studies of the mechanisms regulating ISC divisions allow a better understanding of how adult stem cells integrate different signals to control tissue plasticity, and of how various diseases, notably cancers, arise from their alterations.


2015 ◽  
Vol 308 (10) ◽  
pp. G831-G839 ◽  
Author(s):  
Sean R. Moore ◽  
Marjorie M. Guedes ◽  
Tie B. Costa ◽  
Jefferson Vallance ◽  
Elizabeth A. Maier ◽  
...  

l-Glutamine (Gln) is a key metabolic fuel for intestinal epithelial cell proliferation and survival and may be conditionally essential for gut homeostasis during catabolic states. We show that l-alanyl-l-glutamine (Ala-Gln), a stable Gln dipeptide, protects mice against jejunal crypt depletion in the setting of dietary protein and fat deficiency. Separately, we show that murine crypt cultures (enteroids) derived from the jejunum require Gln or Ala-Gln for maximal expansion. Once expanded, enteroids deprived of Gln display a gradual atrophy of cryptlike domains, with decreased epithelial proliferation, but stable proportions of Paneth and goblet cell differentiation, at 24 h. Replenishment of enteroid medium with Gln selectively activates mammalian target of rapamycin (mTOR) signaling pathways, rescues proliferation, and promotes crypt regeneration. Gln deprivation beyond 48 h leads to destabilization of enteroids but persistence of EGFP- Lgr5-positive intestinal stem cells with the capacity to regenerate enteroids upon Gln rescue. Collectively, these findings indicate that Gln deprivation induces a reversible quiescence of intestinal stem cells and provides new insights into nutritional regulation of intestinal epithelial homeostasis.


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