INTRODUCTION

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Keratins form the intermediate filament cytoskeleton of all epithelial cells. Although it has been demonstrated that this structure is essential for providing cell resilience in epithelia (11, 13), there is little information on individual keratin-specific functions that can account for the complex cell type- and differentiation-specific expression patterns observed in this protein family. Keratin expression is highly regulated in the epidermis. Proliferative basal cells express the keratin pair comprising K5 and K14 (K5-K14 pair). However, when keratinocytes begin terminal differentiation, they move upward, become postmitotic, and switch to the expression of keratin pair K1-K10. Under hyperproliferative conditions (e.g., tumors and wound healing), keratinocytes downregulate K1-K10 and express K6-K16. We recently showed that the ectopic expression of keratin K10 inhibits the proliferation of human keratinocytes, while K16 expression stimulates the process (23). In agreement with this, K10 impairs skin tumor development when ectopically expressed in transgenic mice (29) and K16 overexpression, or ectopic expression, in transgenic mice leads to aberrant epidermal keratinization and hyperproliferation (19, 30).

Keratin K10-induced inhibition of cell proliferation occurs through a process linked to the retinoblastoma protein (pRb) and the molecular machinery controlling cell cycle progression during G₁ (23). The different cellular distributions of keratins (cytoplasmic) and pRb (nuclear) nonetheless suggest that this effect must take place through the K10-mediated impairment of a pathway leading to the functional inactivation of pRb rather than by the direct physical interaction of these two molecules. We selected the ras oncogene-dependent pathway on the basis of a number of findings that imply that K10 and ras could have antagonistic functions in keratinocyte proliferation and differentiation. First, Ha-ras signaling has been implicated in the control of cell cycle progression in a pRb-dependent manner (18, 28), similar to that described for K10 (23). Second, whereas mutations in Ha-ras are early and essential events in mouse skin carcinogenesis protocols (3), K10 is lost during early stages of tumor development. Third, although K10 is expressed in postmitotic, terminally differentiating epidermal cells, transgenic mice expressing a mutant Ha-ras gene from a K10 promoter develop generalized hyperkeratosis of the skin as well as skin tumors (2). Since ras-dependent mitogenic signals diverge through different pathways (see for reviews references 7 and 17), such as those for small GTPases, raf, and phosphoinositide 3-kinase (PI-3K), we studied which of these pathways is specifically affected by K10 expression. The collected data clearly demonstrate that keratin K10 impairs cell cycle progression through the sequestration and inhibition of protein kinase B (PKB; Akt), and atypical PKC.

	MATERIALS AND METHODS

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Plasmids and transfections. The plasmids coding for keratins K1, K10, and K16 have previously been described (23). Plasmids coding for wild-type (wt) and dominant-negative activated Ha-ras, v-raf, and PKC were provided by J. Moscat (Centro de Biologia Molecular, Madrid, Spain). Those plasmids coding for activated forms of RhoA, Rac1, and Cdc42Hs were kindly provided by J. C. Lacal (Instituto de Investigaciones Biomédicas, Madrid, Spain), while those coding for wt and dominant-negative Akt and p110CAAX were from J. Downward (Imperial Cancer Research Fund, London, United Kingdom). The plasmid coding for PDK1 was provided by K. Anderson (Babraham Institute, Cambridge, United Kingdom). Hemagglutinin (HA)-tagged forms of Akt and PKC, as well as myrAkt, were provided by J. S. Gutkind (National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Md.). Plasmid pCDNApRb coding for human wt pRb cDNA (a generous gift from S. Mittnacht) under the control of the cytomegalovirus (CMV) promoter has been previously described (22, 23). pVM6NTermK10 (NTerm) was generated by inserting the HindIII-SacI fragment coding for NTerm (23) into the pVM6 vector (Boehringer Mannheim) in frame with the vesicular stomatitis virus G (VSV-G) tag under the control of the CMV promoter. pRasNTerm was generated by inserting the NTerm-encoding fragment in frame with the sequence encoding Ha-ras at the carboxyl terminus-encoding sequence of pRas[61]F (6). The integrity of the constructs was confirmed by sequencing. Transfections using calcium phosphate or Fugene 6 (Boehringer Mannheim) were performed as previously described (22-27). After selection for 15 to 25 days in the presence of appropriate antibiotics (G418 [0.5 mg/ml] or hygromycin [0.1 mg/ml] or both for cotransfections) colony-forming efficiency experiments were performed at least in triplicate (22-24). Unless otherwise indicated, cells were cotransfected with the same quantity of plasmids coding for K10 and for the different signaling molecules (5 µg of each per p90 dish). The total DNA amount was kept constant in all the transfection experiments, including appropriate amounts of pcDNA3 empty vector. The relative number of colonies was calculated, considering as 100% the number of colonies obtained with empty vectors in each cell line. Data are shown as means ± standard deviations (SD).

Cell culture and immunofluorescence. HaCaT, PB, and MCA3D keratinocytes and C33A and BMGE+H cells were cultured as previously described (21-25). For immunofluorescence analysis after transfection, cells were cultured, fixed, and stained as described previously (22-24) using antibodies against keratin K10 (undiluted supernatants of mouse monoclonal antibody [MAb:] LH1, LH2, or LH3 or 1/40-diluted K8.60 mouse MAb) (21-25). PKC (Santa Cruz Biotechnology or Boehringer Mannheim; both rabbit polyclonal antibodies used at 1/200 and 1/400 dilutions, respectively), Akt (Upstate Biotechnology or Santa Cruz Biotechnology; both goat polyclonal antibodies used at 1/250 and 1/300 dilutions, respectively), phosphorylated Akt (Upstate Biotechnology or BioLabs; both rabbit polyclonal antibodies used at 1/200 and 1/100 dilutions, respectively), and a mouse MAb against VSV-G tag diluted 1/100 (Boehringer Mannheim). Controls, including incubation with preimmune serum, omitting the primary antibody, and preincubation with the immunizing peptide, were routinely performed. Secondary antibodies specific for multiple-labeling purposes were purchased from Jackson Immunoresearch Labs and used as described previously (21-25). Bromodeoxyuridine (BrdU) incorporation and terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assays were performed essentially as previously described (23, 24) using a rat MAb against BrdU (23) and a fluorescein isothiocyanate (FITC)-labeled cell death detection kit (Boehringer Mannheim) in parallel with K10 immunofluorescence (1/40 dilution of antibody K8.60). Specimens were analyzed using a Bio-Rad C600 confocal microscope or an Axiophot conventional immunofluorescence microscope (22-27). Experiments were performed in triplicate; at least 200 transfected cells were scored in each. For triple immunofluorescence, AMCA-labeled antimouse, Texas-red-conjugated antigoat, and FITC-conjugated antirabbit antibodies were simultaneously used.

Immunoprecipitation, immunoblotting, and kinase assays. For coimmunoprecipitation, cell extracts were obtained in phosphoprotein buffer (20 mM Tris [pH 7.5], 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 1% Triton X-100, 2.5 mM sodium pyrophosphate, 1 mM -glycerolphosphate, 1 mM Na₃VO₄, 1 µg of leupeptin/ml, 1 µg of aprotinin/ml, 1 mM phenylmethylsulfonyl fluoride). Protein extracts (50 µg in 500 µl of phosphoprotein buffer) were incubated with agitation (overnight at 4°C) in the presence of 2 µl of antibodies against K10 (mouse MAb K8.60), Akt and PKC (goat and rabbit polyclonal antibodies, respectively, from Santa Cruz Biotechnology), or anti-VSV-G tag (mouse MAb from Boehringer Mannheim). Soluble and keratin-enriched fractions were obtained essentially as described previously (25). Total protein extracts, cytoskeletal enriched fractions, and immunoprecipitates were analyzed by Western blotting as described previously (22-27) using the same antibodies against Akt, PKC, phosphorylated Akt, and VSV-G tag described in "Cell culture and immunofluorescence." Mouse MAb LH3 was used to detect simultaneously K10 and NC. Antibodies against pRb, cycD1, and cycE have been previously described (22, 23). LI0025 was used to detect human K16. The antibodies used in immunoblotting were diluted 1/1,000 to 1/10,000 in Tris-buffered saline containing 0.5% bovine serum albumin and 0.05% Tween 20. To normalize loading, immunoblots were stained with Ponceau S prior to antibody incubations. The kinase activities of Akt and PKC from HaCaT cells cotransfected with 5 µg of K10 or K16 and 2 µg of HA epitope-tagged Akt or PKC were determined upon immunoprecipitation with HA-specific MAb 12CA5 (Babco), using histone 2B (H2B) or myelin basic protein (MBP) as the substrate. Briefly, cells were washed once in cold phosphate-buffered saline and lysed on ice with 1 ml of lysis buffer containing protease and phosphatase inhibitors (1% Triton X-100, 10% glycerol, 137 mM NaCl, 20 mM Tris-HCl [pH 7.5], 1 µg of aprotinin and leupeptin/ml, 1 mM phenylmethylsulfonyl fluoride, 20 mM NaF, 1 mM disodium pyrophosphate, and 1 mM Na₃VO₄). After samples were precleared by centrifugation, lysates were immunoprecipitated with 1 µl of an anti-HA MAb using -binding beads (Amersham Pharmacia Biotech) to sediment immunocomplexes. After three 1-ml washes with lysis buffer, one 1-ml wash with water, and one 1-ml wash with kinase buffer (20 mM HEPES [pH 7.4], 10 mM MgCl₂, 10 mM MnCl₂), reactions were performed (30 min at 25°C) in 30 µl of kinase buffer containing 0.05 mg of the appropriate substrate/ml, 5 µM ATP, 1 mM dithiothreitol, and 10 µCi of [-³²P]ATP. The products of the kinase reactions were fractionated in sodium dodecyl sulfate-15% polyacrylamide gels and radiographically exposed. In some cases, cells were serum starved overnight prior to lysis. When necessary, the same membranes were subsequently probed by Western blotting using the mouse anti-HA (Babco, 1:500) or AE1 (23) MAb to assess the expression level of cotransfected proteins.

Two-cell hybrid experiments. The assay of the interaction between myrAkt and NTerm by the two-cell hybrid approach was performed using the ras rescue system, a modification of the CytoTrap two-hybrid system (Stratagene), essentially as described previously (6). Briefly, yeast temperature-sensitive cdc25-2 cells were cotransformed with the plasmids shown in Fig. 8B. Transformants were cultured on selectable plates and incubated at 25 or 37°C for 5 days. Positive interaction was determined by growth at 37°C in galactose-containing plates. Negative controls included plates with minimal galactose and plates with glucose (not shown).

	RESULTS

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The K10-induced inihibition of cell proliferation is reversed by Akt and PKC. We have previously demonstrated that the expression of keratin K10, but not a mutant K10 lacking both amino and carboxyl ends (NC), induces growth arrest in human HaCaT keratinocytes (23). Although we have also demonstrated that this effect is independent of p53 (23), given that this protein is mutated in HaCaT cells, we analyzed whether keratin K10 was able to inhibit cell growth in other cell types. Figure 1A shows that keratin K10 also compromises cell growth in mouse skin keratinocytes (MCA3D and PB cells) and bovine mammary gland (BMGE+H) cells. However, in agreement with our previous results (23), this effect was not observed in human cervical carcinoma C33A cells lacking functional pRb (Fig. 1A).

View larger version (38K): [in this window] [in a new window]   FIG. 1.   Keratin-induced modulation of cell proliferation is related to signaling effectors belonging to the PI-3K pathway. (A) Keratin K10 (open bars) but not the NC form, which lacks amino and carboxyl termini (solid bars), inhibits cell growth in a variety of epithelial cell lines including human (HaCaT) and mouse (MCA3D and PB) keratinocytes and bovine mammary gland cells (BMGE+H), but not in Rb-deficient human cervical carcinoma (C33A) cells. (B) Keratin K10 also mediates inhibition of HaCaT cell growth when coexpressed with human keratin K1, its natural partner in suprabasal, differentiating keratinocytes of the epidermis (see the introduction). (C) Keratin K10-induced HaCaT keratinocyte cell growth arrest is rescued by coexpression of Ha-ras, PDK1, Akt, and PKC but not by v-raf, RhoA, Rac1, Cdc42, or the activated catalytic subunit of PI-3K (p110CAAX). (D) Western blot using mouse MAb K8.60 (1/10,000 diluted) in lysates of cells cotransfected with K10 and the cited plasmids, demonstrating that the K10 expression levels in these transfections are similar. (E) Colony-forming experiments showing that Akt rescues cell growth inhibition induced by K10 in HaCaT cells in a dose-dependent manner. As a negative control, transfection of increasing amounts of the v-raf-encoding plasmid does not significantly improve the ability of this protein to reverse the K10 inhibitory effect. (F) Akt and PKC functions are necessary to allow normal growth of HaCaT keratinocytes as demonstrated by the reduction in the number of colonies obtained after transfection with 10 µg of dominant-negative forms of Akt or PKC (DNAkt and DNPKC, respectively) relative to the numbers from similar transfection experiments with an empty vector (pcDNA3). A dominant-negative form of Ha-ras (rasN17) was used as a positive control for cell growth inhibition. (G) Transfection of keratin K10 inhibits BrdU incorporation (solid bars) but not apoptosis (TUNEL assay; open bars) in HaCaT. (H) Western blots from protein extracts of pRb-deficient C33A cells transiently cotransfected with K10 or its inactive mutant NC, pRb, and p110CAAX, Akt, PKC, or PDK1, demonstrating that K10-induced repression of pRb hyperphosphorylation and repression of cyclin D1 and E expression are restored by coexpression of PDK1, Akt, or PKC but not by p110CAAX. Numbers, apparent molecular weights (in thousands). Data in panels A to C and E to G are from at least triplicate independent experiments and are shown as means ± SD.

View larger version (29K): [in this window] [in a new window]   FIG. 2.   K16 expression rescues the growth inhibition promoted by PI-3K inhibition. (A) Colony-forming experiments demonstrating that the growth inhibition promoted by wortmannin (Calbiochem; 100 nM), but not by MEK inhibitor PD098059 (Calbiochem; 5 µM), is efficiently rescued by K16 expression. (B) Western blot showing that the expression level of transfected K16 in cells treated with wortmannin is similar to that in cells treated with PD098059. DMSO, K16-transfected cells treated with dimethyl sulfoxide alone.

Transfected K10 interacts with endogenous Akt and PKC and prevents their activation in human keratinocytes. The results showing that effectors of the PI-3K pathway, but not active PI-3K itself, reverse the K10-induced cell cycle arrest suggest that K10 may inhibit the function of such effectors. PI-3K-dependent signals induce changes in the subcellular localization of specific kinases, including Akt and PKC (1, 9). A possible explanation for the inhibitory effect of K10 might be that the presence of this keratin prevents such translocations. This might also explain why the overexpression of the wt forms of these kinases reverses K10-induced cell cycle arrest. To test this hypothesis, we transfected K10 into HaCaT cells and studied the localization of endogenous Akt and PKC by double immunofluorescence and confocal microscopy. In nontransfected cells, these kinases have a diffuse nuclear and cytoplasmic localization (Fig. 3A', B', E, and F). In contrast, in cells expressing transfected K10, this keratin is assembled into the endogenous keratin intermediate filaments (Fig. 3A and B) and most Akt (Fig. 3A') and PKC (Fig. 3B') clearly colocalize along these filaments. Such colocalization was not detected when HaCaT cells were transfected with cell cycle-inactive K10 mutant NC (Fig. 3C, C', D, and D') although this mutant keratin is also integrated into the intermediate filaments formed by the endogenous keratins. Western blot experiments also demonstrated that this effect cannot be attributed to different expression of K10 and NC, since these constructs are expressed to similar levels upon transfection in HaCaT cells (Fig. 3G).

View larger version (103K): [in this window] [in a new window]   FIG. 3.   Akt and PKC colocalize with the keratin cytoskeleton in cells transfected with K10 but not with a mutant form lacking both the amino and carboxyl termini (NC). HaCaT cells were transiently transfected with K10 (A and B) or NC (C and D) and analyzed by double immunofluorescence and confocal microscopy to visualize the transfected keratin (using the LH3 mouse MAb; A to D) and the endogenous Akt (using a goat polyclonal antibody; A' and C') or PKC (using a rabbit polyclonal antibody; B' and D'). (E and F) Distribution of endogenous PKC (E) and Akt (F) in nontransfected HaCaT cells (see also arrows in panels A' and B'). Note that K10, but not NC, changes the distribution of the endogenous kinases from a dispersed to a filamentous shape, such that the distribution colocalizes with that of K10. Similar results were obtained with two different antibodies raised against different epitopes of Akt or PKC (not shown). Arrows (A' and B'), nontransfected cells. Representative examples from three independent experiments are shown. (G) Western blot using MAb LH3 demonstrating that K10 and NC are expressed to similar extents in transfected HaCaT cells (see also Fig. 7B). Bars, 10 µm.

View larger version (99K): [in this window] [in a new window]   FIG. 4.   Impaired activation of PI-3K signaling effectors as a consequence of K10, but not NC, expression. HaCaT cells synchronized in G0 by serum starvation were transfected with K10 (A) or NC (B). After 48 h cells were allowed to reenter the cell cycle by serum addition. After 3 h, expression of the transfected construct (in red) and endogenous phosphorylated Akt (Akt-P; in green) was analyzed by indirect double immunofluorescence. The images shown are derived by merging the two immunofluorescence channels. Note that the expression of K10 leads to nondetectable Akt-P levels, whereas in cells transfected with NC at least some Akt-P (green and yellow) is present. (C and D) Keratin expression alters Akt (C) and PKC (D) activities. HaCaT cells were transfected with K10 or K16 and HA-tagged Akt (C) or PKC (D), and the kinase activities were determined following immunoprecipitation against the HA epitope using H2B and MBP, respectively, as substrates (see Materials and Methods). The lower portions of panels C and D show anti-HA tag immunoblots, demonstrating that similar amounts of immunoprecipitated Akt and PKC are found in the corresponding samples. Representative examples from three independent experiments are shown. Bars, 15 µm.

Akt and PKC interact with K10 during keratinocyte differentiation. The above-described results were obtained upon transfection of keratin K10 in cultured keratinocytes. To determine whether K10 also interacts with Akt and PKC in vivo, we analyzed the cellular distribution of these kinases during keratinocyte differentiation. Since a small proportion HaCaT cells spontaneously differentiate and induce K10 expression (4, 21, 27), we first analyzed the distribution of endogenous Akt and PKC in these spontaneously differentiating cells by double immunofluorescence. It was found that both Akt (Fig. 5A) and PKC (not shown) changed their cellular distributions and colocalized with the endogenous keratin K10-containing filaments (Fig. 5A'). To biochemically confirm these data, confluent HaCaT cultures were induced to differentiate by serum starvation as previously reported (22, 26, 27). The soluble and keratin-enriched fractions were obtained (25) and probed by Western blotting. It was observed that, in undifferentiated cultures, Akt and PKC were mostly present in the soluble fraction (Fig. 5B). In addition, small amounts of these enzymes were observed in the keratin-enriched, insoluble fraction, probably due to the presence of some spontaneously differentiating cells in the culture, as demonstrated by the presence of keratin K10 in this fraction (Fig. 5B). However, in differentiated HaCaT cells, both Akt and PKC were found in the keratin fraction. Finally, the phosphorylated, i.e., active, Akt was detected exclusively in the soluble pool of undifferentiated cells. These results demonstrate that, as observed in transfection (Fig. 3), both Akt and PKC interact with K10 during the differentiation of HaCaT keratinocytes.

View larger version (91K): [in this window] [in a new window]   FIG. 5.   Akt and PKC interact with K10 during HaCaT keratinocyte differentiation. Spontaneously differentiated HaCaT keratinocytes (4, 27) were fixed and analyzed by indirect immunofluorescence to detect endogenous Akt (A) and keratin K10 (A'). Note that in differentiating cells (arrow), characterized by the presence of K10, the Akt staining pattern changes, becoming filamentous and coincident with that of keratin K10 (A''). (B) Akt and PKC are associated with keratins in differentiated HaCaT keratinocyte cultures. HaCaT cells were induced to differentiate by serum starvation for 12 days (22, 26, 27), and the soluble (Sol) and keratin-enriched fractions were obtained as described previously (25) and analyzed by Western blotting using antibodies against keratin K5, keratin K10, Akt, PKC, and Akt-P. Soluble and keratin-enriched fractions from control nondifferentiated cultures were analyzed in parallel. Note the presence of most Akt, PKC, and phosphorylated Akt in the soluble fraction in nondifferentiated cultures (K10 negative), whereas in differentiated cultures both Akt and PKC are in the insoluble (Insol)-keratin fraction, which contains keratin K10. The K5 signal demonstrates similar loadings in the samples from control and differentiating cells.

View larger version (60K): [in this window] [in a new window]   FIG. 6.   Distribution of Akt, Akt-P, and K10 in newborn mouse skin. (A to D) Frozen sections of newborn mouse skin were processed for immunofluorescence using antibodies against Akt (A), Akt-P (B), and K10 (C). The three immunofluorescence channels (Texas red, fluorescein isothiocyanate, and AMCA, respectively) are shown merged in panel D. Note that Akt is present throughout all the epidermal layers, whereas phosphorylated Akt is present exclusively in the basal layer and K10 is restricted to differentiated suprabasal layers. This shows that Akt and K10 are coexpressed in suprabasal cells but that only basal, K10-negative cells have active, phosphorylated Akt. Dashed lines, epidermal-dermal boundary. (E) Immunoprecipitation-Western blot experiments to biochemically confirm the K10-Akt-PKC interaction in skin. Whole-skin extracts were immunoprecipitated (IP) with the indicated antibodies and probed by Western blotting with the antibodies to proteins indicated at the right. Note the presence of K10, but not K5, in Akt and PKC immunoprecipitates and vice versa, whereas phosphorylated Akt is absent from K10 immunoprecipitates. Also note the absence of the kinases in K5 immunoprecipitates. Bar, 100 µm.

The interaction between Akt and PKC and K10 involves the non--helical amino terminus domain of K10. We have previously shown that the non--helical amino and carboxyl terminus domains of K10 are involved in the capacity of K10 to arrest the cell cycle and that the mutant NC form, which lacks these domains, is inactive (Fig. 1A) (23). These ends protrude from the filament core and may mediate interaction with other proteins. We analyzed whether the amino terminus domain of K10 (NTerm) was involved in the interaction with Akt or PKC. We first analyzed whether it has an effect on cell proliferation by itself. For this, the coding sequence for this fragment was subcloned under the control of the CMV promoter in the pVM6 plasmid to provide a VSV-G tag and Neo resistance. Colony-forming experiments showed that NTerm does not inhibit cell proliferation as K10 does (not shown). On the other hand, cotransfection of increasing amounts of NTerm reverses the inhibitory effect of K10 in HaCaT keratinocytes (Fig. 7A) and restores pRb hyperphosphorylation and cyclin D1 expression in C33A cells (Fig. 7B) without affecting the expression of K10 (Fig. 7B). This suggests that this fragment interacts with the same proteins as does intact K10 and that NTerm, present in increasing amounts, competes with filamentous K10.

View larger version (59K): [in this window] [in a new window]   FIG. 7.   Expression of NTerm alleviates K10-induced cell growth arrest. (A) Colony-forming experiments with HaCaT cells demonstrate that the cotransfection of increasing amounts of an NTerm-encoding plasmid with 5 µg of the K10-encoding plasmid rescues K10-promoted inhibition of cell proliferation. (B) Similar cotransfection experiments with C33A cells in the presence of co transfected pRb demonstrate that NTerm also restores transfected pRb phosphorylation and endogenous cyclin D1 levels. Lower two sections demonstrate that the levels of K10 and NC expression are similar and that the expression of increasing amounts of NTerm does not affect the expression of K10. Note also that, unlike K10, NC has no effect on pRb phophorylation and cyclin D1 levels. (C to D'') Examples of triple immunofluorescence after transient cotransfection of 5 µg of K10 and 5 µg of NTerm in HaCaT cells, demonstrating that the colocalization of K10 and endogenous Akt and PKC is abolished in cells expressing NTerm. (C and D) Immunofluorescence visualizing K10. (C' and D') Immunofluorescences visualizing Akt and PKC, respectively. (C" and D") Immunofluorescences visualizing NTerm. For comparison, see Fig. 3A, A', B, and B'. Bars, (C and D), 15 µm. Data in panel A are from triplicate independent experiments and are means ± SD.

View larger version (37K): [in this window] [in a new window]   FIG. 8.   NTerm interacts with Akt in vitro and in vivo. (A) Immunoprecipitation using an anti-VSV-G MAb of extracts from pooled clones of VSV-G-tagged NTerm- and vector-transfected HaCaT cells, followed by Western blotting against VSV-G, Akt, and PKC showing that both Akt and PKC coprecipitate with NTerm. (B) Two-cell hybrid experiments using the ras rescue system (6). cdc25-2 yeast cells were cotransformed with the indicated plasmids and plated at the permissive (25°C) or the restrictive (37°C) temperature onto galactose-containing plates. Note that, besides the positive controls including RasCAAX expression (1 and 3) and pMyrMAFB plus pSOSMAFB expression (6), growth at the restrictive temperature was obtained with the cotransformation of pMyrAkt plus RasNTerm (4), indicating that protein-protein interaction between myrAkt and NTerm has occurred. The absence of growth in 2 demonstrates that NTerm by itself cannot override the mutation of cdc25-2 yeast cells. As a negative control, a myristoylated form of phosduccin D (PhosD) was cotransformed with pRasNTerm (5). No colonies were observed at 37°C in glucose-containing, galactose-depleted plates, indicating that myrAkt alone does not allow yeast cell growth (not shown).

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

Keratin function was long been thought to be mainly structural, until the recent realization that keratin expression may influence cell proliferation and differentiation (19, 23). We have previously demonstrated that K10 inhibits proliferation by reducing cyclin D1 expression and thus pRb phosphorylation (23). Using several approaches, we here show here that these effects are due to the interaction of K10 with Akt and PKC, critical effectors of the PI-3K pathway. We also show that this interaction occurs during the differentiation of human and mouse keratinocytes and involves the non--helical amino terminus of this protein, although we did not determine whether similar interactions also take place through the K10 non--helical carboxyl terminus, which is also involved in cell cycle arrest (23). The binding of Akt and PKC to K10-containing filaments prevents the translocation of these kinases to the membrane and thus their activation. We also demonstrate that this inhibition is responsible for K10-induced cell cycle arrest.

PI-3K activity, for which Akt and PKC are the main specific effectors, has important roles in the control of cell cycle progression. For instance, PI-3K activation is sufficient for cell cycle entry in fibroblasts (14), and the activation of PI-3K and Akt in T lymphocytes promotes pRb phosphorylation and E2F activation (5). Similarly, expression of tumor suppressor PTEN, which dephosphorylates phosphoinositides and thus acts in opposition to PI-3K, inhibits cell cycle progression in a pRb-dependent manner in fibroblasts and keratinocytes (24, 31). In addition, Akt has been identified as a key regulator of cell survival and therefore of oncogenesis. The phosphorylation of cytoskeletal elements, which implies interaction with protein kinases, has been widely reported and appears to control cytoskeleton dynamics (12, 16, 25). Here we show, however, that the interaction of keratin K10 with Akt and PKC also controls the activity of these enzymes by restraining their translocation and subsequent activation. Through this mechanism, keratins affect cell proliferation, differentiation, and apoptosis. Previously reported data also support the possible involvement of the keratins in signal transduction processes. For instance, ectopic expression of K16 in the mouse epidermis, which leads to increased proliferation, also increases the tyrosine phosphorylation of the EGF receptor (19). Further, the overexpression of K8 in the pancreases of transgenic mice leads to phenotypic alterations that mimic the lack of transforming growth factor  signaling (8). In addition, proteosomes, which are involved in the control of cell cycle and signal transduction processes, interact with keratins in a cell cycle-dependent manner (20). The present data demonstrate unexpected and new functional roles for the intermediate filament cytoskeleton and provide evidence for its involvement in the regulation of critical signaling molecules such as Akt and PKC, which may result in the control of cell cycle progression. Further studies will be required to fully understand the increasingly relevant functions that keratins appear to perform in epithelial cells.