Physiological Role of Mitogen-Activated Protein Kinase in Eye

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This entry is adapted from the peer-reviewed paper 10.3390/cells12040617

Mitogen-activated protein kinase (MAPK) pathways represent ubiquitous cellular signal transduction pathways that regulate all aspects of life (such as development of eye) and are frequently altered in disease. Once activated through phosphorylation, these MAPKs in turn phosphorylate and activate transcription factors present either in the cytoplasm or in the nucleus, leading to the expression of target genes and, as a consequence, they elicit various biological responses.

MAPK ERK p38 JNK eye ocular MEK inhibitors

1. Introduction

The mitogen-activated protein kinase (MAPK or MAP kinase) family consists of protein kinases that phosphorylate their own dual serine (Ser) and threonine (Thr) residues (autophosphorylation), or those found on their substrate downstream kinases, to activate or de-activate their target ^[1]. MAPKs are ubiquitously expressed and evolutionarily conserved in eukaryotes. Each group of MAPKs contains a multi-tiered signaling cascade of kinases: at the top upstream level of the canonical MAPK pathways there are the MAPK kinase kinase kinases (MAPKKKKs, or MAP4Ks), which act upon MAPK kinase kinases (MAPKKK, or MAP3Ks), which then act in turn on MAPK kinases (MAPKKs, or MAP2Ks), with a final effector MAPK as their target (Figure 1). MAP3Ks are Ser/Thr protein kinases that are activated through phosphorylation., which, in turn, leads to the phosphorylation and activation of MAP2Ks in their Ser/Thr activation site (Ser-X-X-X-Ser/Thr motif). Activated MAP2Ks then stimulate MAPK activity through dual phosphorylation on Thr and Tyr residues within a conserved Thr-X-Tyr motif located in the activation loop of the MAPK domain ^[2] (Figure 1). A comprehensive list of MAPKs, MAP2Ks and MAPKs is presented in Table 1. MAPKs mainly include four subfamilies based on the conserved Thr-X-Tyr motif: ERK1/2, the JNK1/2/3, the p38 (α, β, γ, and δ), and the ERK5 branches, which are all ultimately activated by signaling cascades initiated by multiple factors such as growth factors and stress. More details on the signaling pathway members are given elsewhere ^[3]. Once activated through phosphorylation, these MAPKs in turn phosphorylate and activate an array of transcription factors present in the cytoplasm and nucleus, leading to the expression of target genes and resulting in a biological response. MAPKs are involved in multiple cellular processes, such as cell differentiation, proliferation, apoptosis, inflammation, stress responses, and immune defense ^[4]. In general, the activation of ERK by growth factors, hormones and proinflammatory stimuli promotes cell proliferation, whereas the activation of p38 and JNK by cellular and environmental stresses promotes multiple cellular processes such as proliferation, apoptosis, immunological effects, insulin signaling and neuronal activity ^[5]. The ERK pathway was the first MAPK cascade to be elucidated and is the best characterized. The canonical intracellular part of the activation pathway starts when a Ras GTPase exchanges a guanosine diphosphate (GDP) for a guanosine triphosphate (GTP) molecule ^[2]. This is facilitated upon the binding of extracellular mitogens to a cell surface receptor such as EGFR and the subsequent docking and activation of intracellular complexes, for instance GRB2-SOS ^[2]. This switching of Ras allows it to activate a MAP3K (e.g., Raf) and initiate the cascade of a MEK1/2 (MAP2Ks) and ERK1/2 (MAPK) activation (Figure 1). More generally, the ERK1/2 pathway is stimulated in mammalian cells by tyrosine kinase receptors and G-protein-coupled receptors through both Ras-dependent and Ras-independent pathways ^[6]. ERK1/2 is also activated by growth factors, mitogens, cytokines, osmotic stress, and in response to insulin ^[2]. Given its central role in cell proliferation, differentiation and survival, the MAPK pathway network and its inhibition has attracted great pharmacological interest in the context of cancer research, and a plethora of compounds have been developed/identified that can directly act on this pathway to influence cell fate.

Figure 1. Simplified schematic summary of the main MAPK signaling pathways.

Table 1. Summary of MAP kinases (up to MAP3Ks) with gene names, protein names and alternative names, the pathways they are known to interact with and their relative level at the signaling cascade.

Gene Name	Protein Name	Alternative Protein Names	Pathway Involved	MAPK Level	Other Gene/Protein Names
MAPK1	ERK2	p42-MAPK	MEK/ERK	MAPK	MAPK2, p38, p40, p41, ERT1, NS13
MAPK3	ERK1	p44-MAPK	MEK/ERK	MAPK	ERT2, PRKM3
MAPK4	ERK4	p63-MAPK	atypical MAPK	MAPK	PRKM4
MAPK6	ERK3	p97-MAPK	atypical MAPK	MAPK	PRKM6, HsT17250
MAPK7	ERK5		ERK5	MAPK	PRKM7, BMK1
MAPK8	JNK1	SAPK1	JNK	MAPK	PRKM8
MAPK9	JNK2	p54aSAPK	JNK	MAPK	PRKM9
MAPK10	JNK3	p54bSAPK	JNK	MAPK	PRKM10, SAPK1b, p493F12
MAPK11	p38 beta	SAPK2, SAPK2B	p38	MAPK	PRKM11
MAPK12	p38 gamma	ERK6, SAPK-3	p38	MAPK	PRKM12
MAPK13	p38 delta	SAPK4	p38	MAPK	PRKM13
MAPK14	p38 alpha	SAPK2A, Mxi2	p38	MAPK	PRKM14, PRKM15, CSBP, EXIP
MAPK15	ERK7/8		atypical MAPK	MAPK
MAP2K1	MEK1	MKK1, MAPKK1	MEK/ERK	MAP2K	CFC3
MAP2K2	MEK2	MKK2, MAPKK2	MEK/ERK	MAP2K	CFC4
MAP2K3	MEK3	MKK3, MAPKK3	p38	MAP2K	SAPKK2
MAP2K4	MEK4	MKK4, MAPKK4	JNK	MAP2K	SAPKK1, JNKK1, JNKK
MAP2K5	MEK5	MAPKK5	ERK5	MAP2K
MAP2K6	MEK6	MKK6, MAPKK6	p38	MAP2K	SAPKK3
MAP2K7	MEK7	MKK7, MAPKK7	JNK	MAP2K	SAPKK4, JNKK2
RAF1	c-Raf	Raf-1	MEK/ERK	MAP3K
BRAF	B-Raf	BRAF-1, RAFB1	MEK/ERK	MAP3K	NS7
MAP3K1	MEKK1		JNK	MAP3K
MAP3K2	MEKK2	MEKK2B	ERK5	MAP3K
MAP3K3	MEKK3	MAPKKK3	ERK5	MAP3K
MAP3K4	MEKK4	MAPKKK4		MAP3K	MTK1, PRO0412
MAP3K5	ASK1	MEKK5, MAPKKK5	JNK and p38	MAP3K
MAP3K6	ASK2	MEKK6, MAPKKK6		MAP3K
MAP3K7	TAK1	MEKK7, TGF1a	JNK and p38	MAP3K	CSCF, FMD2
MAP3K8	MEKK8	Tpl-2, c-COT		MAP3K	COT, EST, ESTF, AURA2
MAP3K9	MLK1	MEKK9		MAP3K	PRKE1
MAP3K10	MLK2	MEKK10		MAP3K	MST
MAP3K11	MLK3	MEKK11	JNK and p38	MAP3K	PTK1, SPRK
MAP3K12	ZPK	MEKK12		MAP3K	DLK, MUK, HP09298
MAP3K13	LZK	MEKK13	JNK	MAP3K	MLK
MAP3K14				MAP3K	FTDCR1B, HS, HSNIK, NIK
MAP3K15	ASK3			MAP3K	bA723P2.3
TAOK1	PSK2	MAP3K16, TAO1	JNK	MAP3K	DDIB, KFC-B, MARKK, hKFC-B
TAOK2	PSK	MAP3K17, TAO2		MAP3K	Tao2beta, PSK1-BETA
TAOK3		MAP3K18	p38	MAP3K	DPK, JIK, hKFC-A
MAP3K19				MAP3K	RCK, YSK4
MAP3K20	MLK7	mlklak, pk		MAP3K	AZK, MLT, MRK, ZAK, SFMMP
MAP3K21	MLK4	dJ862P8.3		MAP3K

The eye is the central organ of the visual system of animals, allowing vision and other, vision-independent photo-response functions by collecting light from the environment and converting the light information to neuronal impulses, ultimately terminating in the brain’s visual cortex. In vertebrates, this is achieved via a complex system of structures which are organized in a spherical organ and serve distinct roles.

2. Physiological Role of MAPKs in the Eye

MAPK/ERK signaling, as a master proliferation and cellular differentiation regulation pathway, is indispensable for the formation of the organism as a whole during development ^[7]. More precisely, ERK kinases play important roles in promoting embryonic survival and regulate the development of the eye in vertebrates. Of note, although the process depicted in Figure 2 is largely conserved within vertebrates, fish such as zebrafish do not form a lens pit and vesicle; rather, the cells from the lens placode proliferate and migrate inwards, directly forming a solid spherical mass that detaches from the surface ectoderm. The formation of the neural retina, RPE and the cornea follow the same process and lineage. In adult goldfish, ERKs are highly expressed in multiple ocular tissues including the lens epithelial cells, lens fiber cells and the retina, whereas its inhibition promotes early apoptosis, preventing the formation of the eye ^[8]. Underscoring the importance of the ERK pathway in development, all RASopathies, which are pathologies due to mutations in the RAS-MAPK pathway, are confined to only gain-of-function mutational defects that lead to inefficient inhibition of the pathway, while there is no documented RASopathy caused by mutational pathway knockout ^[9]; since such mutations should be more common than gain-of-function mutations, their absence signifies that when they occur, are most likely non-viable. Regarding ocular development, morphology and function, RASopathies present only minor clinical manifestations such as the appearance of Lisch nodules, which are aggregates of dendritic melanocytes forming papules in the iris ^[10]. Given its importance for cellular functions, MAPK/ERK signaling has been implicated in multiple organisms in the processes of wound healing and regeneration. For instance, ERK2 is essential for retinal pigment epithelium (RPE) cell proliferation in vitro ^[11]^[12]. Although in mammals, the RPE is post-mitotic in the adult, the mechanisms underlying RPE proliferation are important for stem cell applications and for developmental understanding. MEK–ERK signaling is strengthened by auto-regulation of the expression of constituent molecules in the pathway ^[13], but blockade of initial MEK–ERK signaling inhibits the cell-cycle re-entry of newt RPE cells ^[14], and after wounding in the adult newt ^[15]. The MEK pathway is also essential to switch adult newt RPE cells to neural cells. ^[16]. Regeneration of a complete neural retina can be achieved in larval Xenopus Leavis through the activation of the MAPK signaling pathway by administering exogenous FGF-2 ^[17]. In zebrafish, retina regeneration after injury depends on Müller glia (MG) dedifferentiation into a cycling population of multipotent progenitors via an EGFR/MAPK signal transduction cascade that regulates the expression of regeneration-associated genes such as PAX6 ^[18]^[19]. It should be noted, however, that mammals, unlike teleost fish, do not possess the innate ability for retinal regeneration; rather, mammals develop gliosis after retinal damage. Thus, this knowledge is relevant to humans in the context of stem cell research, the potential for interventions to induce regeneration, or in developmental research. During rat embryogenesis, the ERK1/2 pathway is required for the proper development of retino-geniculate connections ^[20]. FGF2 stimulates PAX6 expression during the induction of transdifferentiation of the RPE through a FGFR/MEK/ERK signaling cascade into a neural-like epithelium ^[21]. Similar transdifferentiation is obtained in chicks through the ectopic expression of a constitutively-activated allele of MEK-1 ^[22]. In the injured chick retina, the MG showed an accumulation of p-ERK1/2 ^[23]. Regarding the JNK activation pathway, the upstream kinases MKK4 and MKK7 have redundant and unique roles in molecular signaling that are important for retinal development, RGC maturation and the response to axonal injury signaling ^[24]. JNK and p38 phosphorylation is increased after retinal ischemia, mainly in amacrine, ganglion and bipolar cells while ERK is activated in MG cells ^[25]. Specific blockage of ERK and p38 phosphorylation, but not of JNK, prevents ischemia-induced apoptosis and improves retinal function in a rat model ^[25]. Other studies have demonstrated, for instance, that in vivo inhibition of p38 MAPK activity may be detrimental to injured photoreceptor cells ^[26]. Thus, the use of p38 MAPK inhibitors for therapeutic purposes must take into account the possible side effects. p38 is activated in retinal ganglion cells (RGCs) after optic nerve axotomy, and this activation is in the signaling pathway for RGC apoptosis ^[27]. MAPK also plays a significant role in MG cell proliferation and differentiation within the retina, in a stage-dependent manner. Prior work strongly supports a model whereby activation of the MAPK signaling pathway promotes the entry of progenitors into a MG cell differentiation pathway during embryonic retinal development, but not after birth ^[28]. For example, Shp2 protein phosphatase deletion abolished ERK phosphorylation in the neural retina, leading to extensive retinal cell death and degeneration. Additionally, Shp2 mediated a basal level of Ras-MAPK signaling in MG cells during postnatal development and in an adult retina under normal physiological conditions ^[29]. Also, the ERK1/2 and p38 MAPK pathways are key regulators of growth cone guidance in vitro ^[30].

Figure 2. Schematic overview of developmental events during mammalian eye development, and germ layer origin of structures in the eye. (A) The optic vesicle, derived from the neuroepithelium of ectodermal lineage, approaches the surface ectoderm where the lens placode (blue cells) forms at the area of proximity between the layers. (B) The optic vesicle forms the optic cup, by the concurrent invagination of both the lens placode, forming the lens pit, and the proximal layer of the optic vesicle to the surface ectoderm, forming the presumptive neural retina (red cells). (C) The lens pit closes up onto itself forming the lens vesicle, with the cells from the central part of the lens pit (blue cells) directed posteriorly, and the cells from the lens pit periphery (yellow cells) directed anteriorly. The optic cup continues to invaginate. (D) The invaginated (inner) layer of the optic cup differentiates into the neural retina (red cells), while the outer layer forms the retinal pigment epithelium, RPE (orange cells). Cells in the posterior surface of the lens vesicle elongate towards the opposite pole, forming the lens fibers and filling the central volume of the lens, while the cells on the anterior side form the lens anterior epithelium. The surface ectoderm closes after the lens vesicle detaches, and the now continuous surface ectoderm forms the cornea.

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Petros Moustardas

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1. Introduction

2. Physiological Role of MAPKs in the Eye

References