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Correspondence to Emmanuelle Caron: e.caron{at}imperial.ac.uk
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Mß2 integrins mediate phagocytosis of opsonized particles in a process controlled by RhoA, Rho kinase, myosin II, Arp2/3, and actin polymerization. Mß2, Rho, Arp2/3, and F-actin accumulate underneath bound particles; however, the mechanism regulating Rho function during Mß2-mediated phagocytosis is poorly understood. We report that the binding of C3bi-opsonized sheep red blood cells (RBCs) to Mß2 increases Rho-GTP, but not Rac-GTP, levels. Deletion of the cytoplasmic domain of ß2, but not of M, abolished Rho recruitment and activation, as well as phagocytic uptake. Interestingly, a 16–amino acid (aa) region in the membrane-proximal half of the ß2 cytoplasmic domain was necessary for activating Rho. Three COOH-terminal residues (aa 758–760) were essential for ß2-induced accumulation of Rho at complement receptor 3 (CR3) phagosomes. Activation of Rho was necessary, but not sufficient, for its stable recruitment underneath bound particles or for uptake. However, recruitment of active Rho was sufficient for phagocytosis. Our data shed light on the mechanism of outside-in signaling, from ligated integrins to the activation of Rho GTPase signaling.
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and ß subunits, which lack catalytic activity. In contrast to the well conserved cytoplasmic domains of ß subunits, subunit cytoplasmic domains share few sequence similarities (Hynes, 2002), which has led to the idea that the two integrin tails play distinct roles and to the suggestion that tails could confer specificity to integrins sharing identical ß chains (Liu et al., 1999; Weber et al., 1999). and/or ß cytoplasmic tails have been involved in several aspects of integrin biology and function (e.g., inside-out signaling, localization to focal adhesions, and cell adhesion; Lu and Springer, 1997; Keely et al., 1999; Weber et al., 1999; Fagerholm et al., 2004). It is thought that both inside-out and outside-in signaling are regulated through the binding of cytoskeletal and regulatory proteins to integrin cytoplasmic regions. Over 20 such proteins have been described to date (Calderwood et al., 2000; Liu and Ginsberg, 2000; Zamir and Geiger, 2001; Tadokoro et al., 2003). Small GTP-binding proteins also play crucial roles in integrin function; Rap1 activity controls inside-out activation of ß1, ß2, and ß3 integrins (Caron, 2003; Bos, 2005), whereas Rho family proteins control integrin signaling to the cytoskeleton (Arthur et al., 2002). However, the molecular mechanisms underlying the cross-talk between integrins and small GTPases remain unclear.
ß2 integrins, which are mutated in type-1 leukocyte adhesion deficiency patients, control the majority of immune cell functions, including cell migration, immunological synapse formation, and phagocytosis (Hogg and Bates, 2000). Accordingly, immune cells isolated from mice that were deficient in one or more ß2 integrins manifested a range of defects in cytoskeletal-based functions (Rosenkranz and Mayadas, 1999). The Mß2 integrin (which is also known as complement receptor 3 [CR3] or CD11b/CD18) is the main phagocytic receptor for particles opsonized with the complement fragment C3bi; as such, it plays a major role in the phagocytosis of microorganisms and apoptotic cells (Gasque, 2004). M and ß2 are both needed for the efficient binding and ingestion of C3bi-opsonized particles (Caron and Hall, 1998), and, similar to Lß2 (Tominaga et al., 1993; Sebzda et al., 2002; Tohyama et al., 2003; Vielkind et al., 2005), Mß2 function is regulated by small GTP-binding proteins (Caron et al., 2000). Interestingly, unlike other modes of uptake, Mß2-dependent phagocytosis relies exclusively on Rho function (Wiedemann et al., 2005). RhoA, but not Rac1, accumulates at sites of particle binding, where it colocalizes with F-actin. A dominant-negative allele of Rho (N19), overexpression of a kinase-dead Rho kinase mutant, or treatment with the Rho kinase inhibitor Y-27632 blocks the recruitment of the actin nucleator/organizer Arp2/3 complex at nascent phagosomes, whereas blockers of Rac and Cdc42 function have no effect (Caron and Hall, 1998; May et al., 2000; Olazabal et al., 2002). RhoA and Rho kinase activities are thus specifically required at phagosomes to drive Arp2/3-dependent actin polymerization and uptake. These results also indicate a striking similarity between the signaling pathways elicited during Mß2-driven phagocytosis and other processes that are mediated by integrins, Rho, and Rho kinase (Liu et al., 2002; McMullan et al., 2003; Ridley et al., 2003; Smith et al., 2003; Worthylake and Burridge, 2003). Nonetheless, the mechanisms involved in Rho regulation downstream of integrin ligation are totally unknown.
We show that the binding of C3bi-opsonized targets to Mß2 activates Rho, but not Rac, in macrophages and Mß2-transfected Cos-7 cells. Moreover, the cytoplasmic domain of ß2, but not of M, controls Rho function during phagocytosis. Remarkably, two distinct regions within the ß2 cytoplasmic tail control Rho activation and stable recruitment. Finally, we show that recruitment of active Rho to nascent phagosomes is sufficient to induce Mß2-dependent uptake.
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Mß2 increases Rho-GTP levelsMß2-mediated phagocytosis requires Rho, but not Rac, activity (Caron and Hall, 1998). To investigate if the levels of active, GTP-bound Rho increase during phagocytosis, we performed pull-down experiments using the Rho-binding domain of rhotekin (RBD) fused to GST, as previously described (Sander et al., 1999). J774.A1 macrophages were pretreated with the phorbol ester PMA, to activate Mß2 binding ability through inside-out signaling (Caron et al., 2000), and challenged with C3bi-opsonized sheep red blood cells (RBCs). At different time points, cells were lysed and levels of active Rho were determined. Progression of phagocytosis correlated with a transient increase in GTP-loaded Rho, peaking 20 min after RBC challenge. A significant increase (up to sevenfold) in GTP-Rho occurred only after stimulation with both PMA and RBCs. The levels of endogenous active Rac1, as determined in the p21-activated kinase (PAK)–CRIB pull-down assay (Sander et al., 1999; Patel et al., 2002), did not change significantly during phagocytosis (Fig. 1 A). These results show that Mß2 ligation by C3bi-opsonized particles (i.e., outside-in signaling) leads to a specific increase in Rho activity.
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M or ß2 and offer a robust alternative system for the study of phagocytosis, as shown by several studies (Rabb et al., 1993; Downey et al., 1999; May et al., 2000). As shown in Fig. 1 B, cells expressing M bound RBCs poorly, and expression of ß2 alone conferred no binding ability. However, as previously reported (Caron and Hall, 1998), coexpression of M and ß2 induced efficient binding and phagocytosis. PMA treatment increases RBCs binding by twofold in transfected COS7 cells, as it does in macrophages and neutrophils. This is not because of increased Mß2 expression, but, rather, because of the activation of regulators of inside-out signaling such as PKC and Rap1 (Caron et al. 2000; unpublished data). Nevertheless, there are clearly enough active integrins in transfected COS cells to bind and zipper around RBC, thereby allowing binding and phagocytosis in the absence of PMA. Coexpression of dominant-negative Rho decreased uptake by 70%, but had no effect on RBC binding (Fig. 1 B). Furthermore, phagocytosis is also accompanied by an increase in the levels of GTP-Rho in transfected Cos-7 cells (Fig. 1 C). No changes in Rac-GTP levels were detected in these cells.
The cytoplasmic domain of ß2 is essential for Mß2-mediated phagocytosis
A mutagenesis strategy was undertaken to identify which regions of Mß2 are responsible for signaling to Rho and phagocytosis. We deleted 14 (M
1139) or 23 (M1130) aa of the M cytoplasmic domain or deleted the whole ß2 cytoplasmic domain (ß2724; Table I) and cotransfected each mutant with its wild-type (wt) counterpart (Fig. 2). At steady-state, M1139/ß2 and Mß2724 were expressed at wt levels, as determined by flow cytometry; however, M1130ß2 did not reach the plasma membrane (unpublished data). The membrane-proximal 10 residues of M, but not the ß2 cytoplasmic tail, are thus important in directing heterodimerization and/or surface expression of the Mß2 integrin.
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Mß2 integrins to bind and internalize C3bi-opsonized RBC. The combination M1139/ß2 led to control levels of binding and uptake. In contrast, deleting the cytoplasmic domain of ß2 (ß2724) increased binding, as described previously for Lß2 (Bleijs et al., 2001), but completely abolished phagocytosis (Fig. 2). The ß2 cytoplasmic domain is therefore necessary for Mß2-mediated uptake.
The cytoplasmic domain of ß2 controls the recruitment and activation of Rho during Mß2 phagocytosis
Accumulation of RhoA at nascent phagosomes can be visualized by expressing a tagged wild-type RhoA construct (Caron and Hall, 1998). In cells expressing full-length Mß2, Rho-GFP was enriched at 60 ± 11% of the phagosomes (Fig. 3, A and B). Interestingly, when coexpressed with wt ß2, M1139 was as able to recruit Rho around RBC as wt M. In contrast, deletion of the ß2 cytoplasmic tail abolished Rho recruitment, reducing it to the background levels observed with GFP alone (Fig. 3 B). Thus, Rho recruitment to early phagosomes during CR3-mediated phagocytosis is controlled by the cytoplasmic domain of ß2.
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Mß2 controlled Rho activation during phagocytosis, we performed rhotekin pull-down assays in cells transfected with the truncation mutants. None of the cytoplasmic deletions influenced Rho-GTP levels in resting cells (Fig. 3 C, open bars). When coexpressed with M1139, ß2 was still able to increase the levels of active Rho in response to RBC (Fig. 3 C, shaded bars). Strikingly, deletion of the ß2 cytoplasmic tail abrogated the RBC-induced increase in GTP-Rho, strongly suggesting that the ß2 cytoplasmic domain controls both Mß2-induced Rho activation and phagocytosis.
A 16-aa acid region in the cytoplasmic domain of ß2 is essential for Rho activation during Mß2 phagocytosis
Additional truncations and point mutations (Table I) were engineered into the ß2 cytoplasmic tail to analyze in detail the regions required for phagocytosis. Ftlow cytometry analysis showed that all the combinations of ß2 mutant chains with wt M were expressed at the cell surface at the same levels as wt ß2, except ß2F766A and ß2AAA, which were consistently expressed at 80 and 50% of the control levels (unpublished data). Interestingly, only three mutants (ß2732, ß2767, and ß2N) showed binding indices similar or superior to wt values. This suggests that, apart from ß2AAA, whose reduced binding ability (Fig. 4 A) correlated with reduced surface expression, all other mutations influence integrin activation and/or recycling. Importantly, the phagocytic capacity of Cos-7 cells transfected with all but two ß2 mutants was low (Fig. 4 B), indicating a possible link between ß2 mutation and the abrogation of Rho function. The exceptions were ß2767, which behaved like wt not only for particle binding but also for phagocytosis, and ß2F766A, which was still able to engulf bound particles efficiently. Interestingly, the ability of ß2 mutants to mediate phagocytosis was correlated with their ability to trigger the accumulation of F-actin at sites of particle binding (Fig. 5).
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747 and ß2755 induced significant Rho activation after phagocytic challenge (Fig. 4 C). In contrast, ß2732 was unable to increase Rho-GTP levels in response to RBC. To confirm the requirement of the 732–747 region of ß2 in Rho activation, we engineered a mutant (ß2N) lacking the NH2-terminal half of the cytoplasmic tail (residues 724–755), thereby missing the putative RhoA activation domain. ß2N was also unable to increase Rho-GTP levels upon RBC binding. Together, these results strongly suggest that the 732–747 region of the ß2 tail is necessary to promote Rho activation during Mß2-mediated phagocytosis, but not sufficient to trigger actin polymerization and uptake.
Threonines 758–760 are essential for ß2-mediated Rho recruitment during CR3-mediated phagocytosis
We next investigated the impact of ß2 mutations on Rho recruitment to nascent phagosomes using confocal microscopy. COOH-terminal deletions of the ß2 cytoplasmic domain had varying impacts on Rho recruitment (Fig. 6 A), suggesting that one or more aa within the 756–767 region of ß2 are required for a detectable accumulation of Rho at phagosomes. Interestingly, several residues within this 12-aa region of ß2 are conserved in other ß chains and proposed to regulate integrin function. In particular, a cluster of threonine residues (758–760) is phosphorylated upon phorbol ester stimulation of leukocytes (Valmu and Gahmberg, 1995) and required for the modulation of leukocyte adhesiveness (Hibbs et al., 1991b; Peter and O'Toole, 1995). Also, mutations in the conserved Asn-Pro-Xaa-Tyr/Phe motif (NPx
, with at positions 754 and 766 in human ß2) perturb the interaction of integrins with binding partners and integrin signaling (Liu and Ginsberg, 2000; Sirim et al., 2001; Calderwood et al., 2002). Thus, we engineered mutants ß2F766A and ß2AAA (threonines 758–760 mutated to alanine) and studied their impact on the recruitment of Rho-GFP to forming phagosomes. Flow cytometry analysis revealed that the ß2F766A mutant was expressed at 80% of the control value at steady-state. This mutant also showed a markedly reduced ability to bind opsonized RBC (Fig. 4 A), but phagocytosis (Fig. 4 B) and Rho recruitment (Fig. 6 A) were both measurable. However, although the ß2AAA mutant was still able to bind particles, it was unable to recruit Rho to nascent phagosomes. In contrast, ß2AAA showed wt binding to a GFP–talin head fragment whose interaction with the ß2 integrin depends on residue F754 (Fig. 6 B). We concluded that the threonine residues at position 758–760 are necessary for Rho recruitment during CR3-mediated phagocytosis.
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755 and ß2AAA were still able to up-regulate Rho activity upon RBC binding (Fig. 4 C and not depicted). This suggests that Rho activation and visible accumulation at sites of particle binding are independent steps and that Rho activation precedes its stable recruitment. In line with this, inactive (N19) Rho is not recruited beneath RBC bound to Mß2 (Fig. 7). To obtain further evidence of the mechanism involved, we analyzed the recruitment of a constitutively active form of Rho (L63) in cells cotransfected with M and ß2 with either wt, AAA, or N (lacking the Rho activation domain but comprising the three threonine residues). Although ß2N cannot activate Rho (Fig. 4 C), coexpression with L63Rho allowed the recruitment of GFP-tagged, active Rho underneath RBC. However, when the experiment was repeated with ß2AAA, L63Rho was no longer recruited to nascent phagosomes (Fig. 7, A and B), confirming our hypothesis that Rho is locally recruited to forming phagosomes in its active, GTP-bound form, in a manner that is dependent on threonines 758–760.
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N and ß2AAA to internalize RBC when coexpressed with wt M and L63Rho-GFP. As shown in Fig. 7 C, coexpression of L63Rho rescued the phagocytic defect of ß2N-expressing cells without affecting their ability to bind RBC or the phagocytic ability of Mß2-expressing cells. Therefore, expression of active Rho completely bypassed the need for the 732–747 region, which is normally necessary for Rho activation, actin polymerization, and phagocytosis (Fig. 4, B and C; and Fig. 5), and allowed both Rho accumulation and RBC uptake by cells expressing the internally truncated mutant. In contrast, cells expressing ß2AAA were not rescued for phagocytosis by L63Rho-GFP (Fig. 7 C). Together, these results indicate that threonines 758–760 control the local accumulation of active Rho, which is sufficient to affect CR3-mediated phagocytosis. |
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Mß2 integrin, which is mainly expressed in macrophages and neutrophils, mediates phagocytosis of microbes and apoptotic cells. Mß2-mediated phagocytosis requires Rap1, RhoA, and Rho kinase activity and is dependent on the Arp2/3 complex and actin polymerization (Caron and Hall, 1998; Caron et al., 2000). Because of its spatially localized signaling, phagocytosis offers an ideal system to understand how extracellular (particularly integrin) ligands regulate the function of small GTP-binding proteins to remodel the actin cytoskeleton. We show that outside-in signaling from the Mß2 integrin requires the cytoplasmic tail of ß2, but not M. Specifically, two distinct subregions within the ß2 tail control the recruitment and activation of RhoA. Interestingly, Rho recruitment to sites of particle binding was dependent on prior activation of the G protein and sufficient for phagocytosis. Our data shed light on the mechanisms by which integrin ligation is coupled to the activation of small GTPase function.
Unlike other modes of phagocytosis or bacterial invasion, Mß2 uptake is dependent on RhoA signaling, but does not require Rac or Cdc42 activity (Wiedemann et al., 2005). Until now, the underlying mechanism had remained unclear. We show that the levels of active, GTP-bound RhoA increase transiently during Mß2 phagocytosis, whereas the levels of active Rac show insignificant variation, suggesting that ligation of Mß2 is sufficient to activate RhoA specifically. In line with this, antibody cross-linking of Mß2 in J774.A1 macrophages also leads to RhoA activation (unpublished data). Whereas Mß2 is so far the only known phagocytic receptor that is exclusively coupled to the activity of the RhoA protein, several studies have previously linked integrin signaling to the up-regulation of Rho activity. For example, a transient up-regulation of RhoA activity was described in human neutrophils freshly plated on immobilized anti-ß2 antibodies (Dib et al., 2001). Although integrin-mediated spreading is associated to Rac1 activation (Price et al., 1998; del Pozo et al., 2000), integrin ligation or overexpression have already been linked to increased RhoA activity in a variety of cell types (Danen et al., 2002; Miao et al., 2002; Zhou and Kramer, 2005).
Mutagenesis revealed that the cytoplasmic domain of ß2 is the main regulator of Mß2 during outside-in signaling to phagocytosis. Maximal cytoplasmic deletions in M that were compatible with surface expression did not alter any of the heterodimer properties that we examined (such as particle binding and phagocytosis and Rho recruitment and activation). In contrast, the phagocytic function of Mß2 was critically dependent on the integrity of the ß2 cytoplasmic domain. Truncation of the entire ß2 tail increased the association of C3bi-opsonized RBC, as previously described (Bleijs et al., 2001), which is consistent with the idea that disruption of intrachain interactions between and ß cytoplasmic domains results in constitutively active integrins (Lu et al., 2001). Except for ß2AAA, for which reduced surface expression correlated with reduced binding, our results suggest that mutations that decrease RBC binding significantly result from an impact of these mutations on integrin inside-out activation or recycling. Indeed, in Mß2 and other integrins, several of the residues between 732 and 766 have been involved in talin binding and activation by Rap1, two important mechanisms in inside-out activation (Garcia-Alvarez et al., 2003; Tadokoro et al., 2003; unpublished data) and in recycling or stimulated internalization (Rabb et al., 1993; Vignoud et al., 1997; Gawaz et al., 2001).
Remarkably, deletion of the entire ß2 tail abolished both RhoA recruitment and activation and also abrogated phagocytosis. Added to the fact that blocking Rho function inhibits RBC uptake without affecting binding, this strongly suggests that Rho activity is specifically required during outside-in signaling from Mß2. This seems to conflict with several papers claiming that RhoA is needed for ß2 activation in lymphocytes and thymocytes (Laudanna et al., 1996; Giagulli et al., 2004; Vielkind et al., 2005). Although it is conceivable that RhoA could regulate either inside-out or outside-in signaling for different integrins or in different cell types, it seems more likely that the discrepancy comes from a different understanding of the readouts used in these studies. Indeed, adhesion to ligand-coated surfaces is not simply a consequence of pure inside-out signaling, but rather a reflection of both inside-out and outside-in signaling. Nevertheless, our results show clearly that the intracellular domain of the ß integrin chain controls RhoA activation.
ß subunits consist of a large extracellular domain, a transmembrane segment, and a relatively short cytoplasmic tail (20–70 aa, 46 in human ß2, except for the much longer ß4 integrin). Truncation of the intracellular region of ß1, ß2, and ß3 abrogates their ability to localize to focal adhesions, and prevents activation of signaling molecules and downstream cytoskeletal remodeling (Solowska et al., 1989; Marcantonio et al., 1990; Hibbs et al., 1991a; Leong et al., 1995; Ylanne et al., 1995). Reciprocally, isolated ß1 and ß3 tails are sufficient to activate focal adhesion kinase and can regulate cell cycle progression and actin cytoskeleton assembly (Tahiliani et al., 1997; Belkin and Retta, 1998; David et al., 1999). Although there is no crystal structure available for any isolated integrin cytoplasmic domain, several groups used nuclear magnetic resonance to investigate the three-dimensional organization of IIbß3 intracellular domains (Vinogradova et al., 2002; Weljie et al., 2002; Garcia-Alvarez et al., 2003). We engineered our truncated ß2 mutants based on their results, which suggested that, in both tails, the membrane-proximal regions were -helical and interacted with each other, whereas the more distal regions are disordered in aqueous environment. Interestingly, we found that two distinct cytosolic regions within ß2 control RhoA activation and recruitment to forming phagosomes. The region controlling Rho activation maps to the helical domain, whereas Rho recruitment is controlled by the TTT motif within the disordered region. Importantly, Rho activation can occur independently of a measurable recruitment. However, the reverse is not true, as nascent phagosomes are negative for RhoA enrichment unless Rho can be activated. There is no Rho recruitment in cells expressing wt Mß2 and N19RhoA or in cells coexpressing wt RhoA and a ß2 mutant harboring an internal deletion of the Rho activation domain, therefore suggesting that only active RhoA can accumulate where RBCs bind. Therefore, there might be a structural basis for the mechanisms underlying Rho recruitment and activation. We also speculate that recruitment of active Rho may play a role in stabilizing the disordered domain of ß2 and possibly of other ß chains.
How could Rho recruitment and activation be coordinately regulated? We describe a specific, transient up-regulation of RhoA activity upon challenge with RBC. The simplest explanation is that, as has been proposed for bacterial invasion, Fc
R-mediated phagocytosis, and various extracellular stimuli, particle binding triggers the local activation of guanine-nucleotide exchange factor molecules (Patel et al., 2002; Rossman et al., 2005; Wiedemann et al., 2005). Because N19Rho, which is thought to titrate endogenous exchange factors, is not recruited to nascent phagosomes, our data might suggest that Rho is activated away from ligated integrins. However, it is hard to envisage how the membrane-proximal RhoA activation domain could direct activation of the GTPase at a distance. The alternative possibility is that RhoA is activated locally. We are currently investigating the possible role of guanine-nucleotide exchange factors, RhoGDI, and, indirectly, GTPase-activating proteins in Rho activation during Mß2 phagocytosis. To explain the local activation of RhoA in the absence of detectable recruitment, we favor the hypothesis that our experimental approach does not allow us to visualize the interaction between overexpressed RhoA and the truncated mutants (e.g., ß2747). This could happen either because the TTT motif is necessary to stabilize the interaction of ß2 with active RhoA, with a regulator of Rho activation, or, finally, because a crucial regulator of Rho recruitment to the truncated mutants is missing in our overexpression setting.
We also found that three threonine residues in the ß2 cytosolic region governed the recruitment of active Rho to nascent phagosomes. Interestingly, the corresponding three-residue sequence, which is flanked by two NPxY/F motifs (Calderwood, 2004), has been associated to the regulation of the adhesive function of ß1, ß2, ß3, and ß7 integrins. However, whether this short sequence is involved in inside-out or outside-in signaling has remained controversial (Hayashi et al., 1990; Hibbs et al., 1991b; Balzac et al., 1993; Peter and O'Toole, 1995; Wennerberg et al., 1998; Calderwood et al., 2001). Our results strongly suggest that residues 758–760 regulate the recruitment of active Rho to the integrin complex in response to ligand binding (outside-in signaling). Phorbol esters were shown to induce phosphorylation of these threonine residues in ß2 (Valmu and Gahmberg, 1995; Fagerholm et al., 2002). As PKC was shown to interact with ß1 tails (Ng et al., 1999), it is tempting to imagine a regulatory mechanism whereby PKC would interact with ß2 and phosphorylate the three threonine residues, allowing the docking of active RhoA (binding either directly or indirectly). Although PKC activity is required for Mß2 phagocytosis (Newman et al., 1991), a role upstream of Rho is hard to reconcile with the observation that mutations in the putative PKC-binding sites on ß2 (Parsons et al., 2002) do not affect Rho recruitment in our model system (unpublished data). Moreover, the ß1–PKC interaction has been connected to increased motility rather than increased adhesion (Ng et al., 1999). Alternatively, it is possible that another as yet unidentified serine/threonine kinase mediates the phosphorylation of these threonine residues. Importantly, several binding partners, including ICAP-1, filamin, and 14-3-3 proteins interact in a phosphorylation-dependent manner with the TTT region of various ß chains (Valmu et al., 1999; Stroeken et al., 2000; Calderwood et al., 2001; Degani et al., 2002; Fagerholm et al., 2002). Unfortunately, none of these molecules has been implicated in Mß2-mediated phagocytosis. Interestingly, however, they are all related to small GTPase signaling (Ohta et al., 1999; Bellanger et al., 2000; Degani et al., 2002; Ueda et al., 2003); 14-3-3 and filamin offer the most direct connection with RhoA signaling, respectively through Rho kinase and binding/activation, via LIM-kinase-induced phosphorylation of cofilin (Arber et al., 1998; Yang et al., 1998; Gohla and Bokoch, 2002). Whether any of these proteins are involved in the stable recruitment of Rho to ß2 integrins during phagocytosis will form the basis of future studies.
In conclusion, we show that ligand binding to Mß2 specifically activates Rho, but not Rac. Rho function is regulated in two steps, which are governed by distinct regions of the ß2 cytoplasmic tail. Whereas a membrane-proximal -helical region controls the activation of Rho, its detectable recruitment involves a distal TTT motif. We demonstrate that stable enrichment of activated Rho at the plasma membrane is controlled by the threonines 758–760 in ß2-cytoplasmic domain and is sufficient to promote Mß2-dependent phagocytosis, a process known to require, successively, Rho kinase, myosin light chain kinase, myosin II, the Arp2/3 complex, and actin polymerization. Because of the conservation of signaling pathways downstream of integrin ß chains, we propose that similar mechanisms operate in related cellular activities, e.g., rear detachment during cell motility.
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The antibodies used in this study were mouse anti-Rac1 (clone 23A8; Upstate Biotechnology), anti-GFP (JL-8; CLONTECH Laboratories, Inc.), anti-myc (9E10; Santa Cruz Biotechnology, Inc), anti-ß2 (BD Biosciences), and rabbit anti-RhoA (119; Santa Cruz Biotechnology, Inc). Conjugated secondary antibodies were obtained from either Jackson ImmunoResearch Laboratories (fluorescence) or GE Healthcare (Western blots).
DNA constructs
Eukaryotic expression vectors (pRK5) encoding human wt ß2, wt M, and myc-tagged N19Rho constructs were previously described (Caron and Hall, 1998), as were pGEX-2T vectors encoding the RBD and the Rac/Cdc42-binding domain of PAK-CRIB (Patel et al., 2002; Dutt et al., 2004). The pRC/CMV plasmid encoding the ß2732 mutant was provided by Y. van Kooyk (VU University Medical Center, Amsterdam, Netherlands).
GFP-tagged small GTPase constructs were generated by subcloning wt, N19, and L63Rho from pGEXRho (Self and Hall, 1995) or pRK5-myc into pEGFP-C1 (CLONTECH Laboratories, Inc.). GFP-talin head was a gift of D.R. Critchley (University of Leicester, Leicester, UK).
M mutants were engineered via PCR by introducing a premature stop codon within the cytosolic tail at positions 1130 (M1130) and 1139 (M1139) using pRK5-M as a template; the sense primer 5'-GCTCTAGACTCTCGAGTACGTGCCACACC-3', which incorporates an internal XhoI site; and the antisense primers 5'-CTTGAAAAGCTTCTA CTTGTACAGCGCGGCGGT-3' for M1130 and 5'-TTCACTAAGCTTCTACTTGTATTGCCGCTTGAA-3' for M1139. ß2 mutants were generated in an analogous manner. Because of unfavorable restriction sites, some required initial subcloning of an Xbal–HindIII fragment of pRK5-ß2 into pUC19. Mutants were cloned by replacing a SacII–HindIII fragment of pUC19-ß2 with different SacII–HindIII PCR fragments, which were amplified using pUC19-ß2 as a template, the sense primer 5'-GCTCTAGAACCCCGCGGCGTGTTGAGTG-3', an incorporated internal SacII site, and one of the following antisense primers: 5'-CAGGTGAAGCTTCTACTTCCAGATGACCAGCAG-3' (ß2724); 5'-CCACTGAAGCTTCTACTTCTCCTTCTCAAAGCG-3' (ß2742); 5'-CGTCGTAAGCTTCTACTTGAAAAGGGGATTATC-3' (ß2755); 5'-CCCCTAAAGCTTCTAACTCTCAGCAAACTTGGGGTTCATGACCGTCGTGGTGGCGCTCTTCCAGATGACCAG-3' (ß2N); 5'-CCCCTAAAGCTTCTAACTCTCAGCAAACTTGGGGTTCATGACCGCCGCGGCGGCGCTCTTGAAAAG-3' (ß2AAA).
The ß2767, ß2747, and ß2F766A mutants were constructed by PCR using wt ß2 as a template, the sense primer 5'-GGGGGGTCTAGAATGCTGGGCCTGCGCCCCCCACTG-3', which incorporates an internal XbaI site, and the following antisense primers: for ß2767, 5'-GGGGGGAAGCTTCTAAGCAAACTTGGGGTTCAT-3'; for ß2747, 5'-GGGGGGAAGCTTCTA CCACTGGGACTTGAGCTTCTC-3'; and for ß2F766A, 5'-GGGGGGAAGCTTCTAACTCTCAGCAGCCTTGGGGTTCAT-3'. The aa sequences of the cytoplasmic tails of all M and ß2 mutants used in this study are given in Table I.
Cell culture and transfection
Cells from the murine macrophage J774.A1 and Cos-7 cell lines, which were obtained from the American Type Culture Collection, were maintained, seeded, and transfected as previously described (Caron and Hall, 1998). For pull-down assays, 9 µg DNA was used to transfect 3 x 105 cells on a 10-cm dish, using SuperFect (QIAGEN) as recommended by the manufacturer. After 4 h, fresh medium was added for 16 h and cells were then serum starved overnight.
Flow cytometry
Transfected Cos-7 cells were washed with cold wash buffer (0.5% BSA and 0.02% azide in PBS) and stained to detect surface ß2, using mouse monoclonal and FITC-conjugated goat anti–mouse antibodies successively. The relative fluorescence of gated Cos-7 cells was analyzed using a FACSCalibur analyzer (Becton Dickinson).
Phagocytic challenge
C3bi-opsonized RBCs were essentially prepared and used to challenge phagocytes as previously described (Caron and Hall 1998), using 0.5 and 20 µl of fresh RBC per coverslip/per dish for immunofluorescence and/or pull-down assays, respectively. For efficient binding and phagocytosis of C3bi-opsonized erythrocytes, macrophages require preactivation (Wright and Jong, 1986; Caron et al., 2000); we routinely pretreated J774.A1 cells with 150 ng/ml PMA in buffered serum-free DME for 15 min at 37°C. PMA-treated cells were washed with warm PBS to remove unbound RBC and fixed in cold 4% paraformaldehyde for 10 min at 4°C.
Immunofluorescence
Transfected Cos-7 cells were first stained for surface ß2. For differential staining of adherent and internalized C3bi-opsonized RBC, cells were incubated with Texas red–conjugated goat anti–rabbit antibodies, permeabilized with 0.2% Triton X-100, and incubated with FITC-conjugated goat anti–rabbit antibodies. Coverslips were finally mounted in Mowiol (Calbiochem) containing p-phenylenediamine (Sigma-Aldrich) as an antifading reagent and analyzed using a fluorescence microscope. Only ß2-positive cells were analyzed; internalized particles (which were red) were easily distinguishable from extracellular RBCs (which were yellow), a property that was used to score phagocytosis. The binding and phagocytic indices are defined as the number of targets bound to and engulfed by 100 phagocytes, respectively. The recruitment of Rho during CR3-mediated phagocytosis was studied by scoring local enrichment in the GFP signal at sites of RBC binding by confocal microscopy (model LSM510; Carl Zeiss MicroImaging, Inc.). A minimum of 20 transfected cells were analyzed per condition. The percentage of bound RBC showing a discrete local enrichment in GFP signal was scored. Phagosomes were scored as positive when at least a quarter of the underlying/surrounding area showed significant GFP enrichment compared with the neighboring areas. All of the overexpressed GFP constructs showed a low level of plasma membrane localization.
GST pull-down assays
Rhotekin RBD and PAK-CRIB fused to GST were prepared as previously described (Ren et al., 1999; Sander et al., 1999). J774A.1 or Cos-7 cell lysates were incubated for 45 min at 4°C with 15 µg of a 50% slurry of glutathione Sepharose 4B beads coupled to GST-RBD-rhotekin or GST-PAK-CRIB to precipitate GTP-RhoA or GTP-Rac. Beads were washed three times in cold lysis buffer (10% glycerol, 1% NP-40, 50 mM Tris, pH 7.6, 200 mM NaCl, 2.5 mM MgCl2, 1 mM PMSF, and protease inhibitor cocktail). Equal volumes of beads and total lysates were analyzed by SDS-PAGE and Western blotting, which were performed as previously described (Patel et al., 2002). Intensities of the RhoA and Rac1 signals were determined by densitometric analysis and related to the levels of total RhoA or Rac1 in the lysates, using the ImageJ software.
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Acknowledgments |
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This research is supported by grants from the Biotechnology and Biological Sciences Research Council (28/C18637) and the Wellcome Trust (068556/Z/02/Z).
Submitted: 10 August 2005
Accepted: 17 February 2006
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