Science,
Journal Year:
2015,
Volume and Issue:
350(6265), P. 1208 - 1213
Published: Dec. 3, 2015
Nicotinamide
adenine
dinucleotide
(NAD(+))
is
a
coenzyme
found
in
all
living
cells.
It
serves
both
as
critical
for
enzymes
that
fuel
reduction-oxidation
reactions,
carrying
electrons
from
one
reaction
to
another,
and
cosubstrate
other
such
the
sirtuins
poly(adenosine
diphosphate-ribose)
polymerases.
Cellular
NAD(+)
concentrations
change
during
aging,
modulation
of
usage
or
production
can
prolong
health
span
life
span.
Here
we
review
factors
regulate
discuss
how
supplementation
with
precursors
may
represent
new
therapeutic
opportunity
aging
its
associated
disorders,
particularly
neurodegenerative
diseases.
The EMBO Journal,
Journal Year:
2021,
Volume and Issue:
40(19)
Published: Aug. 30, 2021
Review30
August
2021Open
Access
Autophagy
in
major
human
diseases
Daniel
J
Klionsky
orcid.org/0000-0002-7828-8118
Life
Sciences
Institute,
University
of
Michigan,
Ann
Arbor,
MI,
USA
Search
for
more
papers
by
this
author
Giulia
Petroni
Department
Radiation
Oncology,
Weill
Cornell
Medical
College,
New
York,
NY,
Ravi
K
Amaravadi
Medicine,
Pennsylvania,
Philadelphia,
PA,
Abramson
Cancer
Center,
Eric
H
Baehrecke
Molecular,
Cell
and
Biology,
Massachusetts
School,
Worcester,
MA,
Andrea
Ballabio
orcid.org/0000-0003-1381-4604
Telethon
Institute
Genetics
Pozzuoli,
Italy
Translational
Sciences,
Section
Pediatrics,
Federico
II
University,
Naples,
Molecular
Human
Genetics,
Baylor
College
Jan
Dan
Duncan
Neurological
Research
Texas
Children
Hospital,
Houston,
TX,
Patricia
Boya
orcid.org/0000-0003-3045-951X
Margarita
Salas
Center
Biological
Research,
Spanish
National
Council,
Madrid,
Spain
José
Manuel
Bravo-San
Pedro
Faculty
Physiology,
Complutense
Networked
Biomedical
Neurodegenerative
Diseases
(CIBERNED),
Ken
Cadwell
Kimmel
Biology
Medicine
at
the
Skirball
York
Grossman
School
Microbiology,
Division
Gastroenterology
Hepatology,
Langone
Health,
Francesco
Cecconi
orcid.org/0000-0002-5614-4359
Stress
Survival
Unit,
Autophagy,
Recycling
Disease
(CARD),
Danish
Society
Copenhagen,
Denmark
Pediatric
Onco-Hematology
Gene
Therapy,
IRCCS
Bambino
Gesù
Children's
Rome,
Rome
'Tor
Vergata',
Augustine
M
Choi
Pulmonary
Critical
Care
Joan
Sanford
I.
York-Presbyterian
Mary
E
Nephrology
Hypertension,
Charleen
T
Chu
orcid.org/0000-0002-5052-8271
Pathology,
Pittsburgh
Pittsburgh,
Patrice
Codogno
orcid.org/0000-0002-5492-3180
Institut
Necker-Enfants
Malades,
INSERM
U1151-CNRS
UMR
8253,
Paris,
France
Université
de
Maria
Isabel
Colombo
Laboratorio
Mecanismos
Moleculares
Implicados
en
el
Tráfico
Vesicular
y
la
Autofagia-Instituto
Histología
Embriología
(IHEM)-Universidad
Nacional
Cuyo,
CONICET-
Facultad
Ciencias
Médicas,
Mendoza,
Argentina
Ana
Cuervo
orcid.org/0000-0002-0771-700X
Developmental
Albert
Einstein
Bronx,
Aging
Studies,
Vojo
Deretic
Inflammation
Metabolism
(AIM,
Excellence,
Mexico
Health
Albuquerque,
NM,
Ivan
Dikic
orcid.org/0000-0001-8156-9511
Biochemistry
II,
Goethe
Frankfurt,
Frankfurt
am
Main,
Germany
Buchmann
Zvulun
Elazar
Biomolecular
The
Weizmann
Science,
Rehovot,
Israel
Eeva-Liisa
Eskelinen
Biomedicine,
Turku,
Finland
Gian
Fimia
orcid.org/0000-0003-4438-3325
Sapienza
Epidemiology,
Preclinical
Advanced
Diagnostics,
Infectious
'L.
Spallanzani'
IRCCS,
David
A
Gewirtz
orcid.org/0000-0003-0437-4934
Pharmacology
Toxicology,
Virginia
Commonwealth
Richmond,
VA,
Douglas
R
Green
Immunology,
St.
Jude
Memphis,
TN,
Malene
Hansen
Burnham
Prebys
Discovery
Program
Development,
Aging,
Regeneration,
La
Jolla,
CA,
Marja
Jäättelä
orcid.org/0000-0001-5950-7111
Death
Metabolism,
&
Disease,
Cellular
Terje
Johansen
orcid.org/0000-0003-1451-9578
Group,
Tromsø—The
Arctic
Norway,
Tromsø,
Norway
Gábor
Juhász
Szeged,
Hungary
Anatomy,
Eötvös
Loránd
Budapest,
Vassiliki
Karantza
Merck
Co.,
Inc.,
Kenilworth,
NJ,
Claudine
Kraft
orcid.org/0000-0002-3324-4701
ZBMZ,
Freiburg,
CIBSS
-
Centre
Integrative
Signalling
Guido
Kroemer
orcid.org/0000-0002-9334-4405
Recherche
des
Cordeliers,
Equipe
Labellisée
par
Ligue
Contre
le
Cancer,
Sorbonne
Université,
Inserm
U1138,
Universitaire
France,
Metabolomics
Platforms,
Gustave
Roussy,
Villejuif,
Pôle
Biologie,
Hôpital
Européen
Georges
Pompidou,
AP-HP,
Suzhou
Systems
Chinese
Academy
Suzhou,
China
Karolinska
Women's
Stockholm,
Sweden
Nicholas
Ktistakis
Programme,
Babraham
Cambridge,
UK
Sharad
Kumar
orcid.org/0000-0001-7126-9814
South
Australia,
Adelaide,
SA,
Australia
Carlos
Lopez-Otin
orcid.org/0000-0001-6964-1904
Departamento
Bioquímica
Biología
Medicina,
Instituto
Universitario
Oncología
del
Principado
Asturias
(IUOPA),
Universidad
Oviedo,
Centro
Investigación
Biomédica
Red
Cáncer
(CIBERONC),
Kay
F
Macleod
Ben
May
Gordon
W-338,
Chicago,
IL,
Frank
Madeo
Biosciences,
NAWI
Graz,
Austria
BioTechMed-Graz,
Field
Excellence
BioHealth
–
Jennifer
Martinez
Immunity,
Laboratory,
Environmental
NIH,
Triangle
Park,
NC,
Alicia
Meléndez
Department,
Queens
City
Flushing,
Graduate
PhD
Programs
Noboru
Mizushima
orcid.org/0000-0002-6258-6444
Tokyo,
Japan
Christian
Münz
orcid.org/0000-0001-6419-1940
Viral
Immunobiology,
Experimental
Zurich,
Switzerland
Josef
Penninger
Biotechnology
Austrian
(IMBA),
Vienna
BioCenter
(VBC),
Vienna,
British
Columbia,
Vancouver,
BC,
Canada
Rushika
Perera
orcid.org/0000-0003-2435-2273
California,
San
Francisco,
Helen
Diller
Family
Comprehensive
Mauro
Piacentini
orcid.org/0000-0003-2919-1296
"Tor
Vergata",
Laboratory
Cytology
Russian
Saint
Petersburg,
Russia
Fulvio
Reggiori
orcid.org/0000-0003-2652-2686
Cells
Systems,
Section,
Groningen,
Netherlands
C
Rubinsztein
Cambridge
Dementia
Kevin
Ryan
Beatson
Glasgow,
Junichi
Sadoshima
Cardiovascular
Rutgers
Jersey
Newark,
Laura
Santambrogio
Sandra
Edward
Meyer
Caryl
Englander
Precision
Luca
Scorrano
orcid.org/0000-0002-8515-8928
Istituto
Veneto
di
Medicina
Molecolare,
Padova,
Hans-Uwe
Simon
Pharmacology,
Bern,
Clinical
Immunology
Allergology,
Sechenov
Moscow,
Fundamental
Kazan
Federal
Kazan,
Anna
Katharina
Kennedy
Rheumatology,
NDORMS,
Oxford,
Anne
Simonsen
orcid.org/0000-0003-4711-7057
Basic
Oslo,
Reprogramming,
Oslo
Hospital
Montebello,
Alexandra
Stolz
orcid.org/0000-0002-3340-439X
Nektarios
Tavernarakis
orcid.org/0000-0002-5253-1466
Biotechnology,
Foundation
Technology-Hellas,
Heraklion,
Crete,
Greece
Sharon
Tooze
orcid.org/0000-0002-2182-3116
Francis
Crick
London,
Tamotsu
Yoshimori
orcid.org/0000-0001-9787-3788
Osaka
Suita,
Intracellular
Membrane
Dynamics,
Frontier
Integrated
Science
Division,
Open
Transdisciplinary
Initiatives
(OTRI),
Junying
Yuan
Interdisciplinary
on
Chemistry,
Shanghai
Organic
Shanghai,
Harvard
Boston,
Zhenyu
Yue
Neurology,
Friedman
Brain
Icahn
Mount
Sinai,
Qing
Zhong
orcid.org/0000-0001-6979-955X
Key
Differentiation
Apoptosis
Ministry
Education,
Pathophysiology,
Jiao
Tong
(SJTU-SM),
Lorenzo
Galluzzi
Corresponding
Author
[email
protected]
orcid.org/0000-0003-2257-8500
Dermatology,
Yale
Haven,
CT,
Pietrocola
orcid.org/0000-0002-2930-234X
Biosciences
Nutrition,
Huddinge,
mor
Frontiers in Cell and Developmental Biology,
Journal Year:
2021,
Volume and Issue:
9
Published: March 29, 2021
Cellular
senescence
is
a
stable
cell
cycle
arrest
that
can
be
triggered
in
normal
cells
response
to
various
intrinsic
and
extrinsic
stimuli,
as
well
developmental
signals.
Senescence
considered
highly
dynamic,
multi-step
process,
during
which
the
properties
of
senescent
continuously
evolve
diversify
context
dependent
manner.
It
associated
with
multiple
cellular
molecular
changes
distinct
phenotypic
alterations,
including
proliferation
unresponsive
mitogenic
stimuli.
Senescent
remain
viable,
have
alterations
metabolic
activity
undergo
dramatic
gene
expression
develop
complex
senescence-associated
secretory
phenotype.
compromise
tissue
repair
regeneration,
thereby
contributing
toward
aging.
Removal
attenuate
age-related
dysfunction
extend
health
span.
also
act
potent
anti-tumor
mechanism,
by
preventing
potentially
cancerous
cells.
program
acts
double-edged
sword,
both
beneficial
detrimental
effects
on
organism,
an
example
evolutionary
antagonistic
pleiotropy.
Activation
p53/p21
WAF1/CIP1
p16
INK4A
/pRB
tumor
suppressor
pathways
play
central
role
regulating
senescence.
Several
other
recently
been
implicated
mediating
Herein
we
review
mechanisms
underlie
growth
particular
focus
why
stop
dividing,
stability
arrest,
hypersecretory
phenotype
how
different
are
all
integrated.
Science,
Journal Year:
2016,
Volume and Issue:
352(6292), P. 1436 - 1443
Published: April 29, 2016
Adult
stem
cells
(SCs)
are
essential
for
tissue
maintenance
and
regeneration
yet
susceptible
to
senescence
during
aging.
We
demonstrate
the
importance
of
amount
oxidized
form
cellular
nicotinamide
adenine
dinucleotide
(NAD(+))
its
effect
on
mitochondrial
activity
as
a
pivotal
switch
modulate
muscle
SC
(MuSC)
senescence.
Treatment
with
NAD(+)
precursor
riboside
(NR)
induced
unfolded
protein
response
synthesis
prohibitin
proteins,
this
rejuvenated
MuSCs
in
aged
mice.
NR
also
prevented
MuSC
mdx
(C57BL/10ScSn-Dmd(mdx)/J)
mouse
model
muscular
dystrophy.
furthermore
that
delays
neural
SCs
melanocyte
increases
life
span.
Strategies
conserve
may
reprogram
dysfunctional
improve
span
mammals.
Science,
Journal Year:
2015,
Volume and Issue:
350(6265), P. 1208 - 1213
Published: Dec. 3, 2015
Nicotinamide
adenine
dinucleotide
(NAD(+))
is
a
coenzyme
found
in
all
living
cells.
It
serves
both
as
critical
for
enzymes
that
fuel
reduction-oxidation
reactions,
carrying
electrons
from
one
reaction
to
another,
and
cosubstrate
other
such
the
sirtuins
poly(adenosine
diphosphate-ribose)
polymerases.
Cellular
NAD(+)
concentrations
change
during
aging,
modulation
of
usage
or
production
can
prolong
health
span
life
span.
Here
we
review
factors
regulate
discuss
how
supplementation
with
precursors
may
represent
new
therapeutic
opportunity
aging
its
associated
disorders,
particularly
neurodegenerative
diseases.