The LKB1 complex-AMPK pathway, the tree that hides the forest
Michaël
Sebbagh1,2,3, Sylviane Olschwang1,2,3, Marie-Josée Santoni1,2,3 and Jean-Paul Borg1,2,3
Initially identified as
the Caenorhabditis elegans PAR-4 homologue involved in early asymmetric
cell division [1], the vertebrate LKB1 gene STK11 [2], also called XEEK1 in Xenopus [3], is conserved throughout evolution
from worms to mammals. In humans, STK11 gene locates on chromosome
9p13.3 and includes 11 exons [2] which encode for two LKB isoforms
by alternative splicing [4, 5]. The long LKB1 (50kDa) form is
detectable from 7 days old embryo and is ubiquitously expressed in adult [6] with a notable higher expression in
pancreas, liver and skeletal muscle [6, 7]. The shorter form (48kDa), which
lacks the last 29 C-terminus residues, appears restricted to testis [5]. Interest in LKB1 has dramatically
increased when it was found to be causally linked to the Peutz-Jeghers syndrome [2, 8], a rare autosomal dominant disorder
characterized by hamartomatous polyposis and mucocutaneous melanin pigmentation [9]. Indeed, in 70% of PJS cases [10], LKB1 kinase activity appears lost
due to genomic deletions [11] or single mutations affecting
either transcript splicing [12] or protein primary structure [11, 13]. Patients affected by this syndrome
have a 18 times higher relative risk of developing cancers at multiple sites,
mostly lung, pancreas, ovary, breast and colon than the general population [14, 15]. This had led to define whether
sporadic mutations of LKB1 gene could occur in tumours. At the exception
of non-small-cell lung cancer where LKB1 is found mutated in 33% of
cases, somatic mutations of this gene are rather rare [16]. Nevertheless, its haploinsufficiency
has been clearly involved in poor outcome for pancreas [17], breast [18], endometrial [19] and liver adenocarcinomas [20]. These observations have led to
classify LKB1 as a tumour suppressor which is a rare feature for a kinase [16].
Generation
of LKB1 knock out (KO) mouse models was the most informative to determine LKB1
functions. Thus, homozygous LKB1 KO mice die at 10.5 days of development mainly
due to defect in neural tube closure and vascular abnormalities attributed, for
this latter, to a VEGF level expression [21]. At the heterozygous state, mice
recapitulate PJS with an average tumour free survival of 43 weeks [22]. In addition, conditional LKB1 KO
mouse models targeting numerous organs confirmed LKB1 suppressor activity in
breast [23], pancreas [24], prostate [25] and skin [26] where tumours appearance is
correlated with an altered cell organization such as the nucleus positioning in
Langerhans b-cells in the case of pancreas [27, 28]. In the same manner, LKB1
deficiency in the thymus prevents peripheral T cell maturation [29] while in the liver this leads to
defects of glucose homeostasis [30]. At the cellular level, LKB1
activity has pleitropic effects. It has been involved in cell cycle arrest [31, 32], apoptosis [33, 34], autophagia [35], energy metabolism [36] as well as in directional cell
migration [37, 38] and epithelial apico-basal polarity [39]. Active LKB1 seems to exert these
cellular effects mainly through phosphorylation, at a conserved N-terminal
residue, of 14 members of the AMPK family kinase which thus become
catalytically actives [40, 41] so driving this wide range of
physiological processes.
In
recent years, research on LKB1, especially on its regulation mode as well as on
its driven functions at cellular level, has been greatly intensified in order
to define how this kinase exerts its tumour suppressor properties. This review
focuses on current knowledge about LKB1 activity regulation, its effectors and
clues on their involvement in cell polarity.
Active LKB1 is a complex
Initial investigations
on LKB1 functions and regulation mechanisms were difficult because of the poor LKB1
intrinsic kinase activity. However, identification of the pseudo kinase STRAD
(STe-20 Related ADaptor) as a LKB1 partner was a real breakthrough since this
association dramatically improves LKB1 kinase activity [42]. Interaction between STRAD and LKB1
appears to be stabilized by a third protein, MO25 (mouse protein25) [43]. This has led to establish that, in
fact, active LKB1 should be considered as a heterotrimeric complex (1:1:1)
hereafter referred to as LKB1 complex (figure 1).
In lower organisms where
the STRAD and MO25 homologues are expressed, even though this has not been
formally established yet, the LKB1 complex formation should be conserved.
Indeed in those organisms, MO25 and STRAD homologues contain the critical residues
required for their activity such as the STRAD C-terminal WEF motif [44]. In mammals, an additional level of
complexity occurs. Indeed, two human STRAD and MO25 paralogues, defined for
both as a and b, have been characterised and appear ubiquitously expressed [43]. Furthermore, at least 4 STRADa [45] and 2 STRADb isoforms [46] all derived by alternative splicing
have been defined. Therefore, cells may express more than one kind of LKB1
complex and in theory could reach up to 16 different ones. Interestingly, some
C-terminus STRADa splice variants, missing their MO25 binding motif, keep their ability to
induce LKB1 kinase activity in vitro [45]. Nevertheless, this aspect remains
unexplored, as LKB1 studies focus almost exclusively on the LKB1-STRADa-MO25a complex, but
should be kept in mind since all these potential complexes could have specific
functions or regulation modes.
The
structure of the LKB1-STRADa-MO25a complex has been recently resolved
and reveals that LKB1 kinase activity results from an allosteric modification
induced by STRADα [44]. Although unable to have an
intrinsic kinase activity, due to absence of critical (Asp-Gly-Phe) residues to
coordinate magnesium binding in its subdomain VII [42], STRADα adopts a conformation close
to an “active” kinase which associates with LKB1 as one of its substrates [44]. In addition, this reveals an unrecognized
STRADα role by promoting interaction between MO25α and LKB1. Indeed, MO25α
plays a crucial role in stabilizing the conformation of the LKB1 activation
loop required for the kinase activity induced by STRADα binding [44]. Thus, this explains how lack of the
LKB1 phosphorylation site in the activation loop, generally required to induce
and stabilize the switch from inactive to active kinase, is dispensable. This
feature leads to the conclusion that LKB1 needs to be associated with STRADα
and MO25α to be active since no LKB1 autophosphorylation would be able to
maintain this active conformation [44].
Regulation of LKB1 complex
Although few things have
been clearly established on this point, the fact that LKB1 can phosphorylate
and activate almost all known members of the AMPK family kinase implies that
the LKB1 complex should be sharply regulated to trigger specific responses. Crystal structure had
confirmed that LKB1 complex activity is regulated through the LKB1/STRAD
interaction. Since expression level or stability of STRAD or LKB1 proteins does
not appear to be involved in LKB1 complex regulation, the eventuality that
post-translational modifications could be involved has been investigated.
Post-translational modifications
Several phosphorylation
sites have been defined on LKB1. Four threonines phosphorylated through
LKB1-STRAD interaction are considered as autophosphorylation sites revealing
LKB1 complex activity [42]. In the same conditions, STRADa
phosphorylation sites have also been identified, though these sites are not
conserved in the STRADb paralogue [44]. LKB1 Thr363 is phosphorylated
after DNA damage in an ATM kinase-dependent manner [47, 48]. This phosphorylation does not
modify LKB1 complex catalytic activity, but has been recently demonstrated to
be required for inactivation of CRTC2, a transcriptional coactivator of CREB, a
critical component of germinal center for B cell proliferation [48]. Even if LKB1 Ser325 and 428,
respectively phosphorylated by at least ERK and p90RSK, do not affect LKB1
complex kinase activity [49, 50] they have interestingly been described
to impede LKB1 inhibitory effect in anchorage-independent growth, concomitantly
to a reduction of AMPK activation [49-51]. Phosphorylation on several other
LKB1 sites like Ser31 or Thr189 has also been observed, but kinases involved
and functional consequences are still unknown [52]. However, these sites do not appear
to be involved in LKB1 complex activity since their substitution by alanine
does not significantly affect the LKB1 kinase activity measured in vitro [52]. LKB1 can also be farnesylated at a
C-terminal CAAX sequence only present in the LKB1 long form. This modification
gives rise to LKB1 higher affinity for membrane localization, as alanine replacement
of the critical cysteine in CAAX sequence abolishes it [47, 53, 54]. Nevertheless, farnesylation does
not affect LKB1 complex activity [49, 51]. The only LKB1 post translational
modification referred to modulate kinase activity of the complex is
acetylation. Indeed, it has been reported that LKB1 could be acetylated on nine
different lysines. Among those, acetylation of the LKB1 Lys48 reduces its
affinity for STRADa and then decreases activity of the complex [55]. Although the acetyl transferase responsible
for this modification has not been identified yet, SIRT1 appears to be as the deacetylase
able to remove this acetyl group and then favour LKB1 complex formation and
activity [55]. These observations suggest that
LKB1 complex activity is not mainly regulated by a post translational
modification, even though some of them have functional consequences [50]. Furthermore, to our knowledge, no
studies have still observed LKB1 complex activation under any stimulating cues,
leading to the hypothesis that LKB1 complex could be constitutively active [51, 53] and that its regulation may dependent
on its intracellular localization [53].
Subcellular localisations
LKB1 complex localization
in cells was initially investigated in over-expressing systems using tagged
constructs [42, 56-58]. It was then observed that LKB1
predominantly localizes in the nucleus and to lesser extent in the cytosol. A
nuclear localization signal (NLS) at the N-amino terminal of LKB1 was found to
be critical for LKB1 nuclearization [56-58]. Interestingly, overexpressed STRADa is clearly
able to displace LKB1 from the nucleus to the cytoplasm compartment [42, 43, 56] whereas STRADb was unable to
do so [56]. Thus, it was proposed that active
LKB1/STRADa was cytosolic whereas the nuclear LKB1 was active through its
interaction with STRADb [56]. Nevertheless, recent results
challenge this model. Indeed, improvement of LKB1 serological tools allowed to
immunostain endogenous LKB1. Results from those experiments, confirmed by cell
fractionation assays, show that endogenous LKB1 localizes mainly in the
cytosolic and membrane fractions and appears to be absent from the nucleus [4, 53]. Failure to detect endogenous
nuclear LKB1 has been reported in different cell types, leading to reconsider
the functional relevance of the identified NLS sequence. In addition, while
LKB1 functions appear to be largely conserved throughout evolution, its C.
elegans or Drosophila homologues do not have NLS sequence and are
not significantly found in the nucleus [54].
Endogenous LKB1
immunostaining in migrating cells shows LKB1 concentration at the leading edge [38]. In the same way, in fully
polarized epithelial cells LKB1 localizes in a E-cadherin dependent manner at
the basolateral domain [38, 53] overlapping with adherens junctions [38, 53]. Farnesylation is required for this
membranous localization and, more importantly, membranous LKB1 colocalizes and
interacts with STRADa thus supporting complex activity at
basolateral domain [53]. This endogenous LKB1 complex
localization at the plasma membrane has also been observed in C.elegans [59]. In Drosophila, although
STRAD has not been localized yet, LKB1 was observed at the cell cortex [54, 60]. Functionally, the LKB1 complex
presence at the basolateral domain is correlated to its ability to activate one
of its substrate, AMPK [53], suggesting that LKB1 complex
regulation could be governed through its intracellular localization allowing
proximity with its substrates. This eventuality is strengthened by sparse
observations in which LKB1 Ser431 phosphorylation reduces its affinity for the
membrane [4] as well as its ability to properly
activates AMPK [50].
Altogether, this gives
rise to the idea that the LKB1 complex is constitutively active and regulation
of cellular processes in which it is involved appears dependent of its
subcellular localizations. Very recently, a second LKB1 localization identified
in primary cilium of polarized epithelial cells [61] strengthen this hypothesis,
nevertheless mechanism(s) regulating these spatial segregations remain to be
defined.
LKB1 complex effectors and substrates
Effectors
LKB1 effectors
have been identified mainly by mass spectrometry and yeast two hybrid assays.
Thus, LKB1 was found to interact with the Hsp90/Cdc37 protein complex contributing
likely to its cellular stability [62, 63]. LKB1 was also reported to interact
with LIP1 (LKB1 interacting protein 1) which contains 6 Leucine rich repeats
(LRR) [64]. Function of LIP1 and consequences
of its interaction with LKB1 remain elusive even though effects on TGFb signalling
pathway have been suggested [64]. In the same manner, LKB1
interaction with PTEN [65] was observed without clear evidence
of functional consequences. Although poorly investigated in the LKB1 context,
potentially through LIP1, TGFb and PTEN have been described to be involved in
several syndromes like juvenile polyposis which leads to formation of gastrointestinal
hamartomas bearing different histological features [66]. Nevertheless, since mechanisms responsible
for the formation of those benign polyps are still undefined, deregulation of
the cross talk between TGFb, through SMAD4, and mTOR pathway negatively
regulated by PTEN and LKB1 [36], could play a role in these
pathologies. In addition, LKB1 was also described to interact with Estrogen
receptor-a (ERa) [67] and with Brahma related gene-1 (BRG1) [68], both involved in transcriptional
regulation. Nevertheless, LKB1 does not appear to phosphorylate these latest
partners suggesting perhaps potential indirect LKB1 effect [67, 68].
LKB1 complex substrates, the AMPK related kinase family
AMPK (AMP kinase) was the first LKB1
substrate identified and it is, by far, the one to have been better characterised [69, 70]. This kinase is a heterotrimer
composed of a catalytic (AMPKα) and two regulatory (AMPKβ and AMPKγ) subunits. AMPK is activated when
the intracellular AMP/ATP ratio increases, for instance during hypoxia or
nutrient deprivation. In these conditions, LKB1 complex kinase activity does
not increase but cytosolic accumulated AMP binds to AMPKg subunit [71] allowing, by allosteric
modification, the accessibility to the critical threonine of the AMPK T-loop
kinase domain targeted by LKB1 complex, so leading to its phosphorylation and
then to AMPK activation. Main interest in this LKB1 substrate comes from the
indication that AMPK modulates the activity of multiple downstream targets such
as Raptor (Regulatory associated protein of mTOR) which, in turn, repress the mTORC1 pathway [36]. mTORC1 integrates growth factors
and nutriment inputs and controls eukaryote cell growth deregulated in most
human tumours [72]. Thus, LKB1 could be the link
between energy metabolism and tumour growth suspected since more than 50 years [51]. This hypothesis is particularly
attractive to explain the mechanism by which LKB1 exerts its tumours suppressor
activity. However, AMPK activation could occur by multiples alternative ways
than through the LKB1 complex. Indeed, AMPK can be
activated by alternative kinases such as CAMKKβ (Ca2+/calmodulin-dependent protein kinase kinase β) [73] or TGFb-activated kinase-1
(TAK1) [74] which probably contribute to some consequences
attributed to LKB1 complex. Details about AMPK regulated pathways, especially its
involvement in mTOR pathway and cell contractility regulation, are reviewed by Tomi
Makela and al. in this issue. However and even though AMPK involvement in LKB1
functions appears until now preponderant, the LKB1 complex is able to activate 13
other kinases [47] belonging to the AMPK family which are poorly studied
compare to AMPK (figure 2). Most of these kinases have
been confirmed to be activated by LKB1 in physiological conditions since their
activity is significantly reduced in Lkb1-deficient models.
Among
them, the two
brain-specific kinases (BRSK-1 and -2) also called SAD kinases (SAD-B
and –A), mainly expressed in brain and testis, play a role in neuronal
cell polarity. BRSK deficient mice exhibits drastic reduced axon growth as well
as mislocalized axons and dentritic markers [75, 76]. In addition, BRSK-2 has been
demonstrated to regulate centrosome duplication. Indeed, BRSK-2 localizes at
centrosome through its association with g-Tubulin and phosphorylates it at
serine 131 which is required to centrosome duplication [77]. Thus, BRSK-2 could regulate
polarity and neuronal proliferation as AMPK does for epithelial cells (see below).
Moreover, like AMPK, BRSK-2 can be also phosphorylated and activated,
independently from LKB1, notably by CAMKK [78].
The LKB1
complex had been described to phosphorylate the four human MARK kinases (microtubule affinity regulating kinase), homologous
to the C. elegans Par-1 gene product [40]. Even though, MARK
kinases appear involved in epithelial cell polarity [79, 80], the relationship between LKB1 and MARK kinases
remain unclear in mammals. Indeed, LKB1 deficiency either in primary
fibroblasts or in cardiac muscle cells does not lead to
significant modifications of MARK3 phosphorylation and activation [40]. This could be explained by the fact that TAO1 kinase
(Thousand and one amino acid protein kinase) is able to phosphorylate the
critical T-loop threonine and thereby activate MARK kinases [81]. Nevertheless, forced expression of active LKB1 triggers
MARK2 function by suppressing tubulin polymerization through Tau
phosphorylation and affecting cell migration and polarity [82]. Thus, in physiological conditions, MARK kinase
activation by LKB1 could be restricted to some isoforms.
Like for
other related AMPK kinases, activation of QSK and SIK kinases is due to their phosphorylation on
the T-loop threonine by LKB1. For these kinases, this motif is a docking site
for the 14-3-3
family members which participates to their full activation and concomitantly
affects their subcellular localization [41]. Indeed, an active form of QSK localizes in punctate structures
of unknow nature within the cytosol through 14-3-3 binding [41]. While QSK functions are not well established, QSK
knockdown in Drosophila triggers mitotic defects like spindle and
chromosome alignement abnormalities indicating that this protein might be
involved also in cell proliferation [83]. In addition to the indication that both Drosophila
AMPK and LKB1 deficiencies lead to similar defects [84, 85], it is tempting to
speculate that those three kinases may cooperate in a same pathway during Drosophila
cell division, potentially linked to energetic stress.
SIK1 (salt-induced kinase 1) has been
described to play a role in steroidogenesis and TGFb signalling, for this latter by
inhibiting type I TGFb receptor kinase [84]. More recently, SIK1 was also found
to have a crucial role in p53 dependent apoptosis induced by cell detachment,
called anoïkis [33]. This study shows that following
cell detachment, SIK is activated in a LKB1 dependent pathway triggering p53
phosphorylation and apoptosis through proapoptotic Bax and Puma induced
expression. Thus, loss of LKB1, SIK1 or p53 interferes in anoïkis induction so
favouring metastasis development [33]. SIK2, also called QIK,
appears to be highly expressed in adipose tissues and is able to phosphorylate
insulin receptor substrate 1 (IRS1) at the same site than AMPK [85]. Similarly, SIK2 phosphorylates the CREB coactivator TORC2 at the same site than AMPK,
leading to TORC2 capture by 14-3-3
proteins. Result of this binding is TORC2 retention in the cytosol preventing
its transcriptional induction of gluconeogenic genes expression [85].
About NUAK2,
also referenced as ARK5, few things are known, except that mice deficient for
this kinase exhibit an embryonic lethality after 16.5 days of development due
to an exencephaly which results in a brain protrusion outside the skull [86]. Moreover, NUAK2 has been described to be activated
through TNFa, leading to inhibition of the actomyosin contractile network through
phosphorylation of threonine 696 and 853 of MYPT1 regulatory subunit of the
myosin light chain phosphatase. Thereby, this inhibition induces increased
phosphorylation of myosin light chain and cellular contractility [87]. Unfortunately, this study does not link this TNFa-dependent NUAK2 activity
with the LKB1 complex.
Nevertheless, NUAK1 activated by LKB1 complex has been found recently to
lead to similar effect on MYPT1 [88]. This suggests that, through NUAK kinases, LKB1 could
play an important role in cell contractility regulation independently of Rho
GTPAses family effector such as Rho
kinase [87]. Besides, NUAK1 has been reported to be increased in
colorectal tumours where it promotes invasiveness [89]. NUAK1 is also involved in cell senescence [90] and apoptosis inhibition [91]. Beyond an already established connection between
cell contractility and apoptosis [92], contractility driven by NUAK1 could have a major
role in tumorogenesis progress in addition to these well established roles in
invasion and metastatic processes.
Finally,
SNRK, the less studied member of AMPK related kinases, is mainly expressed
in testis and might be involved in spermatogenesis or spermatozoid motility [93]. This idea is coherent with the fact that male mice
which express low levels of LKB1 are sterile [94].
LKB1 and cell polarity
From the seminal studies
in C.elegans, that characterized PAR4, the LKB1 homologue and its involvement
in asymmetric cell division, implication of this kinase in cell polarity and
cell division had been suspected [1]. LKB1 contribution in cell cycle
regulation was confirmed by ectopic expression in various cellular models
leading to induction of p21waf Cdk inhibitor in a p53 dependant manner [31, 32]. Beyond this effect on cell cycle
regulation, the LKB1 complex could be directly involved in cell division
process, as its knock down in Drosophila S2 cells affects chromosome
alignment, spindle formation and centrosome number [83]. These effects could be the result
of loss of either QSK, MARK-3 or AMPK activities which are individually
important in cell division [83]. Nevertheless, those findings
remain fragmentary and need to be confirmed in mammalian models.
In addition to PAR4, Kemphues and colleagues
had characterized other genes involved as partitioning defective mutants that
include mammalian PAR3 and PAR6 co-homologues. These proteins are well
established cell polarity proteins and act together with PAR1 and PAR5, homologues
of MARK kinases and 14-3-3
respectively. Thus, the role of LKB1 in cell polarity establishment was
initially investigated and observed in Drosophila
oocyte polarization [54]. In mammals, LKB1 complex
contribution to apico-basal cell polarity was revealed by co-expressing STRADa and LKB1 in
colorectal cancer cell lines [39]. Indeed, in those cells, forced
LKB1 activity induced leads to formation of brush border-like structures and an
actin cap resembling to the apical domain of polarized epithelial cells [39]. Moreover, this apical-like domain
was concomitantly associated with directed endosomal transport of basolateral
markers, such as the transferin receptor, excluded from the apical structure [39]. However, LKB1 involvement in
epithelial cell polarity is less obvious than usually considered. Indeed,
several reports describe that LKB1 knock-down in MDCK [53, 61] or CaCo2 [53] cells derived respectively from
canine kidney or human colon, only exhibits a slight delay in cell polarity. Moreover,
during embryonic development of LKB1 deficient mice, no cell polarity defect is
observed until 7 days of development while important processes of cell
polarization have already taken place before this stage [21]. Studies in Drosophila can
potentially explain this discrepancy. Indeed, it has been shown that AMPK or
LKB1 loss leads to defects in Drosophila epithelial cell polarity only
under energetic stress [60]. These results suggest that
LKB1-AMPK is required to allow cell adaptation to unfavourable growth
conditions, probably because epithelial cell polarity maintenance is an
energetic consuming process. It would be interesting to define whether, in
mammalian cells, a similar mechanism is conserved. Indeed, during epithelial
derived tumours formation loss of polarity could be due not only to loss of
structural protein functions but result also to limiting nutriment availability
leading to an energetic stress that tumour cells have difficulties to bypass.
Thus, observations that E-cadherin is partly involved in LKB1 dependent AMPK
activation [53] and often lost during tumour
progression [95], could reflect another way for it
to affect cell polarity in addition to its well established structural
functions [96]. This eventuality is strengthened
by the fact that AMPK activity, involved in tight junction formation [97, 98], is increased in epithelial cells
through calcium switch [97, 98] considered in part to act on
E-cadherin and adherens junctions formation. Main role of the tight junctions
is to seal the apical membranes of adjacent epithelial cells precluding the
free diffusion of solutes toward the basolateral membranes [99]. However, they also restrict the
lateral diffusion of some lipids and plasma membrane-associated proteins
between apical and basolateral domains, which is thought to ensure that the two
membrane domains do not mix [99]. How AMPK activity controls these
events is unclear. It seems that its inhibitory properties on the mTOR pathway
may play a role, since the effect of dominant negative AMPK construct on tight
junctions formation can be partially rescued by mTOR inhibitors such as
Rapamycin [97]. This is consistent with the fact
that mTOR activity is opposed to apico-basal polarity by contributing to the
epithelio-mesenchymal transition [100]. All of this underlines that
outside of energetic stress conditions where LKB1-AMPK appears to be dispensable
in epithelial cell polarity, the mTOR pathway activity should be maintained low
by an alternative mechanism. Moreover, MARK kinase activities, well known to be
required in epithelial cell polarity [79, 80] would be also activated through a
LKB1 independent manner potentially by TAO1 kinase as mentioned above [81].
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