Control of mitochondrial function and cell growth by the atypical cadherin Fat1

Longyue L. Cao, Dario F. Riascos-Bernal, Prameladevi Chinnasamy, Charlene M. Dunaway, Rong Hou, Mario A. Pujato, Brian P. O'Rourke, Veronika Miskolci, Liang Guo, Louis Hodgson, Andras Fiser, Nicholas E S Sibinga

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Mitochondrial products such as ATP, reactive oxygen species, and aspartate are key regulators of cellular metabolism and growth. Abnormal mitochondrial function compromises integrated growth-related processes such as development and tissue repair, as well as homeostatic mechanisms that counteract ageing and neurodegeneration, cardiovascular disease, and cancer. Physiologic mechanisms that control mitochondrial activity in such settings remain incompletely understood. Here we show that the atypical Fat1 cadherin acts as a molecular brake' on mitochondrial respiration that regulates vascular smooth muscle cell (SMC) proliferation after arterial injury. Fragments of Fat1 accumulate in SMC mitochondria, and the Fat1 intracellular domain interacts with multiple mitochondrial proteins, including critical factors associated with the inner mitochondrial membrane. SMCs lacking Fat1 (Fat1 KO) grow faster, consume more oxygen for ATP production, and contain more aspartate. Notably, expression in Fat1 KO cells of a modified Fat1 intracellular domain that localizes exclusively to mitochondria largely normalizes oxygen consumption, and the growth advantage of these cells can be suppressed by inhibition of mitochondrial respiration, which suggest that a Fat1-mediated growth control mechanism is intrinsic to mitochondria. Consistent with this idea, Fat1 species associate with multiple respiratory complexes, and Fat1 deletion both increases the activity of complexes I and II and promotes the formation of complex-I-containing supercomplexes. In vivo, Fat1 is expressed in injured human and mouse arteries, and inactivation of SMC Fat1 in mice potentiates the response to vascular damage, with markedly increased medial hyperplasia and neointimal growth, and evidence of higher SMC mitochondrial respiration. These studies suggest that Fat1 controls mitochondrial activity to restrain cell growth during the reparative, proliferative state induced by vascular injury. Given recent reports linking Fat1 to cancer, abnormal kidney and muscle development, and neuropsychiatric disease, this Fat1 function may have importance in other settings of altered cell growth and metabolism.

Original languageEnglish (US)
Pages (from-to)575-578
Number of pages4
JournalNature
Volume539
Issue number7630
DOIs
StatePublished - Nov 24 2016

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Cadherins
Growth
Smooth Muscle Myocytes
Aspartic Acid
Mitochondria
Respiration
Muscle Neoplasms
Adenosine Triphosphate
Muscle Mitochondrion
Cell Respiration
Muscle Development
Kidney Neoplasms
Vascular System Injuries
Mitochondrial Proteins
Mitochondrial Membranes
Vascular Smooth Muscle
Oxygen Consumption
Hyperplasia
Blood Vessels
Reactive Oxygen Species

ASJC Scopus subject areas

  • Medicine(all)
  • General

Cite this

Control of mitochondrial function and cell growth by the atypical cadherin Fat1. / Cao, Longyue L.; Riascos-Bernal, Dario F.; Chinnasamy, Prameladevi; Dunaway, Charlene M.; Hou, Rong; Pujato, Mario A.; O'Rourke, Brian P.; Miskolci, Veronika; Guo, Liang; Hodgson, Louis; Fiser, Andras; Sibinga, Nicholas E S.

In: Nature, Vol. 539, No. 7630, 24.11.2016, p. 575-578.

Research output: Contribution to journalArticle

Cao, LL, Riascos-Bernal, DF, Chinnasamy, P, Dunaway, CM, Hou, R, Pujato, MA, O'Rourke, BP, Miskolci, V, Guo, L, Hodgson, L, Fiser, A & Sibinga, NES 2016, 'Control of mitochondrial function and cell growth by the atypical cadherin Fat1', Nature, vol. 539, no. 7630, pp. 575-578. https://doi.org/10.1038/nature20170
Cao LL, Riascos-Bernal DF, Chinnasamy P, Dunaway CM, Hou R, Pujato MA et al. Control of mitochondrial function and cell growth by the atypical cadherin Fat1. Nature. 2016 Nov 24;539(7630):575-578. https://doi.org/10.1038/nature20170
Cao, Longyue L. ; Riascos-Bernal, Dario F. ; Chinnasamy, Prameladevi ; Dunaway, Charlene M. ; Hou, Rong ; Pujato, Mario A. ; O'Rourke, Brian P. ; Miskolci, Veronika ; Guo, Liang ; Hodgson, Louis ; Fiser, Andras ; Sibinga, Nicholas E S. / Control of mitochondrial function and cell growth by the atypical cadherin Fat1. In: Nature. 2016 ; Vol. 539, No. 7630. pp. 575-578.
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abstract = "Mitochondrial products such as ATP, reactive oxygen species, and aspartate are key regulators of cellular metabolism and growth. Abnormal mitochondrial function compromises integrated growth-related processes such as development and tissue repair, as well as homeostatic mechanisms that counteract ageing and neurodegeneration, cardiovascular disease, and cancer. Physiologic mechanisms that control mitochondrial activity in such settings remain incompletely understood. Here we show that the atypical Fat1 cadherin acts as a molecular brake' on mitochondrial respiration that regulates vascular smooth muscle cell (SMC) proliferation after arterial injury. Fragments of Fat1 accumulate in SMC mitochondria, and the Fat1 intracellular domain interacts with multiple mitochondrial proteins, including critical factors associated with the inner mitochondrial membrane. SMCs lacking Fat1 (Fat1 KO) grow faster, consume more oxygen for ATP production, and contain more aspartate. Notably, expression in Fat1 KO cells of a modified Fat1 intracellular domain that localizes exclusively to mitochondria largely normalizes oxygen consumption, and the growth advantage of these cells can be suppressed by inhibition of mitochondrial respiration, which suggest that a Fat1-mediated growth control mechanism is intrinsic to mitochondria. Consistent with this idea, Fat1 species associate with multiple respiratory complexes, and Fat1 deletion both increases the activity of complexes I and II and promotes the formation of complex-I-containing supercomplexes. In vivo, Fat1 is expressed in injured human and mouse arteries, and inactivation of SMC Fat1 in mice potentiates the response to vascular damage, with markedly increased medial hyperplasia and neointimal growth, and evidence of higher SMC mitochondrial respiration. These studies suggest that Fat1 controls mitochondrial activity to restrain cell growth during the reparative, proliferative state induced by vascular injury. Given recent reports linking Fat1 to cancer, abnormal kidney and muscle development, and neuropsychiatric disease, this Fat1 function may have importance in other settings of altered cell growth and metabolism.",
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AU - Riascos-Bernal, Dario F.

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AU - Dunaway, Charlene M.

AU - Hou, Rong

AU - Pujato, Mario A.

AU - O'Rourke, Brian P.

AU - Miskolci, Veronika

AU - Guo, Liang

AU - Hodgson, Louis

AU - Fiser, Andras

AU - Sibinga, Nicholas E S

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AB - Mitochondrial products such as ATP, reactive oxygen species, and aspartate are key regulators of cellular metabolism and growth. Abnormal mitochondrial function compromises integrated growth-related processes such as development and tissue repair, as well as homeostatic mechanisms that counteract ageing and neurodegeneration, cardiovascular disease, and cancer. Physiologic mechanisms that control mitochondrial activity in such settings remain incompletely understood. Here we show that the atypical Fat1 cadherin acts as a molecular brake' on mitochondrial respiration that regulates vascular smooth muscle cell (SMC) proliferation after arterial injury. Fragments of Fat1 accumulate in SMC mitochondria, and the Fat1 intracellular domain interacts with multiple mitochondrial proteins, including critical factors associated with the inner mitochondrial membrane. SMCs lacking Fat1 (Fat1 KO) grow faster, consume more oxygen for ATP production, and contain more aspartate. Notably, expression in Fat1 KO cells of a modified Fat1 intracellular domain that localizes exclusively to mitochondria largely normalizes oxygen consumption, and the growth advantage of these cells can be suppressed by inhibition of mitochondrial respiration, which suggest that a Fat1-mediated growth control mechanism is intrinsic to mitochondria. Consistent with this idea, Fat1 species associate with multiple respiratory complexes, and Fat1 deletion both increases the activity of complexes I and II and promotes the formation of complex-I-containing supercomplexes. In vivo, Fat1 is expressed in injured human and mouse arteries, and inactivation of SMC Fat1 in mice potentiates the response to vascular damage, with markedly increased medial hyperplasia and neointimal growth, and evidence of higher SMC mitochondrial respiration. These studies suggest that Fat1 controls mitochondrial activity to restrain cell growth during the reparative, proliferative state induced by vascular injury. Given recent reports linking Fat1 to cancer, abnormal kidney and muscle development, and neuropsychiatric disease, this Fat1 function may have importance in other settings of altered cell growth and metabolism.

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