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Heat shock proteins (HSPs) derived from tumors or virally infected cells can stimulate antigen-specific CD8+ T cell responses in vitro and in vivo. Although this antigenicity is known to arise from HSP-associated peptides presented to the immune system by major histocompatibility complex (MHC) class I molecules, the cell biology underlying this presentation process remains poorly understood. Here we show that HSP 70 binds to the surface of antigen presenting cells by a mechanism with the characteristics of a saturable receptor system. After this membrane interaction, processing and MHC class I presentation of the HSP-associated antigen can occur via either a cytosolic (transporter associated with antigen processing [TAP] and proteasome–dependent) or an endosomal (TAP and proteasome–independent) route, with the preferred pathway determined by the sequence context of the optimal antigenic peptide within the HSP-associated material. These findings not only characterize two highly efficient, specific pathways leading to the conversion of HSP-associated antigens into ligands for CD8+ T cells, they also imply the existence of a mechanism for receptor-facilitated transmembrane transport of HSP or HSP-associated ligands from the plasma membrane or lumen of endosomes into the cytosol.
Activation of the T cell limb of the adaptive immune system involves the recognition of small ligands bound to MHC or MHC-like proteins on plasma membranes. This antigen presentation paradigm is best understood for peptides associated with MHC class I or class II molecules, with a large body of work having defined two distinct pathways by which protein antigens are converted to shorter fragments occupying the polymorphic binding domains of these MHC glycoproteins 1. For MHC class I molecules, peptides are mainly created by the action of proteasomal enzymes on proteins present in the cytosol. These peptides are then transported by the transporter associated with antigen processing (TAP) dimer through the membrane of the endoplasmic reticulum (ER), after which they are bound to nascent MHC class I heavy chain–β2-microglobulin complexes within the ER lumen 2. The occupied MHC molecules then pass through the secretory pathway to the cell surface where they can interact with the receptors of CD8+ T cells. MHC class II molecules instead interact primarily with large polypeptides within various endosomal compartments 345, after which exopeptidases remove the unprotected segments of the antigen outside of the MHC molecule binding groove 67. The resulting MHC class II–peptide complexes are then exported to the plasma membrane for recognition by CD4+ T cells.
Heat shock proteins (HSPs) are highly conserved peptide-binding molecules that control the folding of proteins and prevent their aggregation 8. The same peptide-binding capacity appears to allow HSPs to acquire proteinaceous antigenic material within cells, and when administered exogenously, to induce priming of CD8+ T lymphocytes in vivo 910111213. This property suggests that there is efficient transfer of antigen from HSPs to MHC class I molecules under these conditions. Such transfer is surprising both because peptide loading of MHC class I molecules typically involves a cytosol to ER route, and because while we understand the role of several well-defined receptor systems in facilitating MHC class II–peptide presentation 1415161718, little is known about any specific pathways for capture and delivery of exogenous antigens to (intracellular) MHC class I molecules. In circumstances other than those known to involve HSP 19202122, MHC class I presentation of peptides derived from exogenous protein sources has been reported and ascribed to either endosomal degradation of particulate antigens, followed by “regurgitation” of the derived peptides for loading of surface class I molecules 23, or to delivery of antigens from endosomes and/or phagosomes into the cytosol by an unknown route 24252627. The relative contribution of either of these proposed pathways to presentation of HSP-associated antigen has not been determined, nor is much known about the cell biology of such exogenous pathways for MHC class I–peptide acquisition.
Several groups have recently reported that various HSP molecules show cell surface binding and/or cellular uptake that in some 2829 but not other 30 cases has the characteristics expected of a saturable receptor system. However, these studies did not link these binding events to functional antigen presentation, or address by what route the antigen in the bound HSP is converted into peptides associated with MHC class I molecules. Given other studies showing active signaling by HSP for induction of cytokine secretion by various cell types 31, it was possible that the binding reported in these earlier investigations was related to this functional stimulation and not necessarily to antigen presentation. Here, we analyze HSP delivery of antigenic material to MHC class I molecules using both functional and morphologic methods. Our data reveal that saturable uptake of the complexes, apparently through interaction with one or more surface receptors, is important for delivering HSP-associated antigen to the cell for processing via either an endosomal or a cytosolic route. Which processing pathway is preferred appears to depend on the sequence context of the antigenic peptide bound to the HSP. The evidence presented here for proteasome-dependent processing of HSP-derived material also implies the existence of an uncharacterized mechanism for transport of HSP complexes, or their cargo, across plasma or endosomal membranes into the cytosol.
Macrophages were collected by peritoneal lavage 6 d after injection of 1 ml of thioglycollate into C57BL/6 or (C3H × C57BL/6)F1 mice (The Jackson Laboratory). B3Z is a CD8+ T cell hybridoma specific for OVA 257–264 (SIINFEKL) bound to H-2Kb MHC class I molecules 32. 3A9 is a CD4+ T cell hybridoma specific for the hen egg lysozyme determinant corresponding to residues 46–61 bound to the MHC class II molecule I-Ak 33.
Recombinant HSP 70 protein was expressed from the pMS236 plasmid constructed by cloning the 1.96-kb NcoI-XbaI fragment of the genomic mouse clone hsp70.1 34 into the pTrc99 expression vector (Amersham Pharmacia Biotech). Expression in DH5α cells was induced by 1 mM isopropyl-β-d-thiogalactopyranoside (IPTG), harvested cells were disrupted, and clarified supernatants were loaded onto a DEAE Sephacel column (Amersham Pharmacia Biotech). Elution of HSP 70 was achieved by applying a 25–500 mM NaCl gradient. Fractions containing HSP 70 were loaded onto an ATP-agarose column (Sigma-Aldrich), and elution was achieved by applying a 0–1 mM ATP gradient. Fractions containing HSP 70 were precipitated with 80% ammonium sulfate, redissolved in low salt buffer containing magnesium acetate, dialyzed against the same buffer, and aliquots were stored at −80°C. Bovine HSP 70 was purchased from Sigma-Aldrich.
The loading of mouse HSP 70 was performed as described previously 11 with minor variations. The HSP and the hybrid peptide (synthesized by Bio-Synthesis, Inc.) were incubated together in PBS containing 1 mM KCl, 2 mM MgCl2, and 100 μM ATP for 45 min at room temperature. 1 mM ADP was added, and the incubation was extended for an additional 30 min. The free hybrid peptide was removed by extensive washing using a Centricon 30K (Amicon), until the residual free hybrid peptide was calculated to be in the picomolar range. The efficiency of the loading was determined with iodine-labeled hybrid peptide to be ~20% in most preparations.
105 thioglycollate-induced macrophages were cultured overnight in each well of a flat-bottomed 96-well plate in the absence or presence of the indicated antigens and 5 × 104 B3Z or 3A9 cells in a final volume of 200 μl. As an indication of the T cell activation, IL-2 accumulation in the supernatant at 16 h was measured by ELISA (BD PharMingen) 26. For the competition experiments, macrophages were preincubated with the indicated amount of unloaded bovine HSP 70 (Sigma-Aldrich) for 30 min at 37°C in a final volume of 100 μl. Without washing, loaded HSP 70 or antigenic peptide was then added along with 5 × 104 B3Z cells, and incubation continued for an additional 16 h before assay of IL-2 accumulation. Error bars show SEM; where no bars are visible, the errors were too small to plot.
(C57BL/6 × C3H)F1 macrophages were cultured for 8 h with the indicated antigens in the presence or absence of 25 μM lactacystin (Calbiochem). The APCs were then fixed with 1% paraformaldehyde for 10 min at room temperature, treated for 10 min with 0.1 M glycine, washed, and cultured overnight with either B3Z or 3A9 T cell hybridoma cells. IL-2 accumulation in the supernatant at 16 h was measured as an indication of T cell activation.
Bovine HSP 70 (Sigma-Aldrich), BSA (Sigma-Aldrich), and 25-D1.16 (an mAb specific for the SIINFEL/Kb complex [see reference 41]) were biotinylated using N-hydroxy succinimide–biotin (Pierce Chemical Co.) according to the manufacturer's directions. FITC-OVA (Molecular Probes) was used at a concentration of 200 μg/ml. Rabbit anticalnexin (StressGen Biotechnologies) and FITC-conjugated mouse anti–rabbit antibodies (Jackson ImmunoResearch Laboratories) were used at 5 μg/ml. Steptavidin–Texas red (Southern Biotechnology Associates) was used at 2 μg/ml. Biotinylated 25-D1.16 was used at 10 μg/ml. Details of intracellular staining analyzed by immunofluorescence confocal microscopy are given in the legend to Fig. 3. Details of the surface staining and internalization assay, analyzed by immunofluorescence confocal microscopy, are given in the legend to Fig. 4. In brief, 5 × 105 thioglycollate-induced macrophages were grown overnight in 24-well plates on poly-l-lysine (Sigma-Aldrich) coated coverslips. The next day, the coverslips were washed to remove the nonadherent cells and incubated with the indicated antigens in 250 μl of complete medium. Cells were fixed with 1% paraformaldehyde (see Fig. 3) or with 3% paraformaldehyde (see Fig. 4) followed by quenching with 0.1 M glycine. Unless otherwise indicated, cells were permeabilized with 0.1% Brij. In Fig. 4 A, cells were stained with Streptavidin–Texas red without permeabilization. Coverslips were mounted with Fluorosave (Calbiochem). Digital images were acquired using a Leica LSCM, composed in Adobe Photoshop®, and printed after formatting in ClarisDraw.
For saturation binding analysis, 5 × 105 thioglycollate-induced macrophages were incubated with increasing concentrations of either biotinylated HSP 70 or biotinylated BSA for 45 min on ice, then washed. For the binding competition assay, macrophages were incubated first with the indicated amount of unlabeled HSP 70 or BSA for 45 min on ice, and followed without washing by incubation with biotinylated HSP 70 for an additional 45 min. Cells were washed two times and incubated with Streptavidin-PE (Molecular Probes) and FITC-CD11b (BD PharMingen), then washed again. Data were collected using a FACScan™ flow cytometer (Becton Dickinson) after addition of propidium iodide and analyzed using CELLQuest™ software (Becton Dickinson). Gates were set for CD11b+, propidium iodide–negative cells, and either flow histograms of HSP staining of CD11b+ cells staining were generated (competition experiment), or mean fluorescence values of HSP staining for this cell subpopulation were calculated (saturation analysis).
To gain a better understanding of HSP antigenicity, with its implications for both the basic biology of antigen presentation and the development of HSP-based vaccines, we first addressed whether the proposed “regurgitation” route or the cytosol to ER route, or both, contributes to the presentation of HSP-associated antigen. This was accomplished by examining the effects of inhibiting proteasome activity or eliminating TAP function on T cell stimulation by HSP/antigen complexes. Mouse HSP 70 was loaded in vitro with synthetic antigens containing the amino acid sequence SIINFEKL (residues 257–264 of OVA) that is presented by H-2Kb. The binding motif of HSP 70 consists of a hydrophobic core of four to five amino acids and two flanking regions enriched in basic residues 835. Because SIINFEKL does not contain this motif, we synthesized hybrid peptides containing a sequence derived from BiP that binds avidly to HSP 70 and that is connected to SIINFEKL via a GSG linker at the antigenic peptide's NH2 terminus (HWDFAWPWGSGSIINFEKL, referred to as BiP-OVA) or the converse (SIINFEKLGSGHWDFAWPW, referred to as OVA-BiP). The two different orientations of SIINFEKL and BiP motif were tested because the sequence context of a MHC class I–binding determinant within a protein has been shown to affect its efficiency of presentation 3637. With both of these hybrid peptides, the loading efficiency of HSP 70 was typically 20%, versus only 1% occupancy using antigenic peptides not optimized for HSP binding (11; and data not shown). These HSP/hybrid peptide complexes are highly effective at priming CTL responses in vivo 38.
In the presence of macrophages as APCs, HSP 70 loaded with either BiP-OVA (HSP/BiP-OVA) or OVA-BiP (HSP/OVA-BiP) stimulated IL-2 secretion from the SIINFEKL/Kb-specific T cell hybridoma B3Z, whereas neither hybrid peptide added alone to macrophages was effective (Fig. 1). This excludes the possibility that activation achieved using HSP/hybrid peptide complexes is mediated by residual free peptide and suggests that an active cellular process is necessary for generation of the SIINFEKL/Kb ligand. HSP 70 itself, or HSP 70 mixed with hybrid peptides under conditions that do not support stable complex formation, was not immunogenic. Taking into account the 20% loading, the HSP/antigen complexes were as efficient on a molar basis as the potent optimal-length free SIINFEKL peptide, despite their requirement for additional processing.
The role of proteasomal enzymes in the presentation of SIINFEKL from the HSP 70/antigen complexes was examined by incubating peritoneal macrophages with either of the HSP/hybrid peptide complexes in the presence of the potent proteasomal inhibitor lactacystin 39. Only stimulation by HSP/OVA-BiP, but not by HSP/BiP-OVA, was substantially inhibited by lactacystin used at 25 μM, a concentration that did not influence presentation of free SIINFEKL peptide or of an endosomally processed determinant of hen egg lysozyme that binds to MHC class II molecules (Fig. 2 A). Such selective inhibition argues against either a general toxic effect or a nonspecific inhibition of cellular proteases, and suggests that HSP can use two distinct intracellular processing pathways to deliver antigenic peptides to MHC class I molecules, only one of which involves proteasome activity. To further define these pathways, we tested the role of TAP. TAP-deficient macrophages express lower levels of MHC class I molecules at the cell surface than wild-type cells, but this limitation can be overcome by growing the cells at reduced temperature in β2-microglobulin 40. TAP−/− macrophages were therefore grown at 26°C for 24 h and transferred to 37°C when incubation with the antigens and the T cells was started. In agreement with the data obtained using lactacystin, TAP-deficient macrophages showed greatly impaired presentation of SIINFEKL from HSP/OVA-BiP but not from HSP/BiP-OVA (Fig. 2 B).
These functional experiments suggest that HSP/OVA-BiP is preferentially processed via the classical class I pathway and imply that the HSP/ligand complex, or the ligand alone, is translocated into the cytosol after which proteasomal cleavage and TAP transport contribute to MHC class I loading of released peptide in the ER. In contrast, HSP/BiP-OVA appears to be predominantly processed by a distinct pathway. To visualize directly the site(s) of SIINFEKL-MHC class I association after exposure of cells to HSP/antigen complexes, macrophages were incubated with each of the HSP complexes, and the cells were stained with 25-D1.16, an mAb to SIINFEKL/Kb complexes 41. Compared with cells exposed to HSP only (not shown), we could detect SIINFEKL/Kb complexes with 25-D1.16 when macrophages were incubated with either of the HSP/antigen preparations. In agreement with the implications of the antigen presentation studies, the intracellular distribution of these MHC class I/peptide complexes varied depending on the antigen employed. With HSP/BiP-OVA, whose presentation is insensitive to proteasomal inhibition and is TAP independent, a vesicular staining predominates (Fig. 3 A). 25-D1.16 staining (Fig. 3 C) partially colocalizes with OVA internalized by fluid phase endocytosis (Fig. 3D–E), indicating that with this HSP/antigen combination, SIINFEKL-loaded MHC class I molecules are found preferentially in endosomes. In contrast, when macrophages are pulsed with HSP/OVA-BiP, the staining of vesicular structures is infrequent (Fig. 3 B), and the 25-D1.16 staining (Fig. 3 F) largely colocalizes with calnexin used to identify the ER (Fig. 3G and Fig. H). Together with the above data on proteasome and TAP dependence of HSP/OVA-BiP presentation, these staining data support the existence of an HSP-mediated pathway for the translocation of polypeptides into the cytosol, in agreement with a recent study involving a lymphoma cell line 30.
These functional and morphologic results thus reveal that two distinct routes of processing can lead to MHC class I presentation of HSP-associated antigenic material, and also suggest that which pathway is preferentially used depends on the relationship of the class I binding sequence to the surrounding peptide structure. Having a free COOH-terminal anchor residue (BiP-OVA) seems to be associated with effective processing by an endosomal route. In contrast, having this key binding residue within an extended polypeptide chain (OVA-BiP) appears to require proteasomal action for efficiently placing this amino acid at the COOH terminus of the processed material 4243. Additional peptide sequences will need to be tested to determine if this is truly a general rule, which would have important implications for the design of HSP-based vaccines.
The efficiency of presentation using HSP/hybrid peptide complexes suggests the existence of a specific mechanism that can maximize the available pool of antigenic substrate within the cell. Several recent studies have provided evidence for receptor-mediated binding of various HSPs to cell surfaces 28 and/or receptor-mediated uptake into endosomes 2829. To look for evidence of a receptor uptake system under the conditions employed here, we examined the interaction of biotinylated HSP with peritoneal macrophages. Incubation with biotinylated HSP 70 at 4°C resulted in binding to the cell surface (Fig. 4 A). The bound HSP was internalized into endocytic vesicles when the cells were warmed to 37°C (Fig. 4 B), where it partially colocalized with OVA provided as a fluid phase marker (Fig. 4C and Fig. D). This binding and rapid endocytic uptake were specific to HSP 70, as biotinylated BSA gave no surface staining at 4°C and little concentration in vesicles after a longer time at 37°C under these conditions (not shown). These data are in agreement with and extend recent results showing that glucose-regulated protein (Grp) 96 and heat shock cognate protein (HSC) 70 can bind to the plasma membrane and internalize into endosomal-like structures 2829.
The surface binding observed microscopically could also be detected using flow cytometry. Only 25–30% of isolated peritoneal macrophages, a population composed largely of the CD11b-brightest cells (data not shown), exhibited substantial cell surface binding of biotinylated HSP 70 (Fig. 4 E). Interestingly, this matches the proportion of HSP-pulsed macrophages that can be lysed by CTLs specific for HSP-associated antigen 12. Thus, the level of surface receptor expression correlates with and may determine effective presentation of HSP-associated ligand. Consistent with the existence of a saturable, specific receptor system, surface binding of biotinylated HSP to the CD11bbright cells could be partially but substantially inhibited by a 10-fold excess of unlabeled HSP, but not by BSA (Fig. 4 E), and exposure to increasing concentrations of HSP 70 resulted in staining approaching a plateau at 200 μg/ml among the CD11bbright cells (Fig. 4 F). A 10-fold excess of unloaded HSP (100 μg/ml) also substantially inhibited B3Z responses to either of the HSP/hybrid peptide complexes (Fig. 4 G), in accord with the idea that the receptor-mediated binding observed by staining contributes to antigen presentation by both processing pathways detailed above.
The evidence provided here for both a cytosolic and endocytic route for MHC class I presentation of HSP-associated antigen provides new mechanistic insight into a well-recognized functional property of HSP. The two pathways we have directly visualized correspond to those previously proposed to underlie presentation of material associated with artificial particulate antigens or with bacteria 2324252627. In our own previous study of latex bead–associated protein, the efficiency of MHC class I–dependent antigen presentation was low, which we considered inconsistent with the operation of a highly evolved specific pathway 26. In contrast, HSP-mediated antigen presentation is quite efficient and our congruent microscopic and functional evidence support the existence of a specific receptor uptake system for HSP/antigen complexes, extending both morphological data and extensive quantitative uptake data from other recent studies 2829 by showing a functional relationship between such receptor-dependent surface binding and HSP-dependent MHC class I antigen presentation.
Receptor-mediated uptake improves MHC class II antigen presentation by up to four orders of magnitude 1415161718. The presumably similar enhancing effects of such uptake on the HSP-dependent presentation pathway, together with the expression of these putative receptors on subsets of professional APCs involved in initiating immune responses (including splenic dendritic cells [Castellino, F., unpublished results]), strongly imply that class I, and possibly also class II, MHC molecule presentation of HSP-associated antigens is a physiologically relevant pathway. The heterogeneity seen for HSP 70 binding to peritoneal mononuclear cells suggests that expression of the HSP binding structures is regulated during cellular differentiation, whereas the continued small increment in staining observed at very high HSP concentrations (>200 μg/ml; our unpublished observations) raises the possibility that more than one affinity class of receptor may exist. The staining at very high HSP concentrations could reflect weak cross-binding among the different receptors proposed by Arnold-Schild et al. to mediate Grp 96 versus HSP 70 binding 28.
Antigen cross-presentation plays a key role in responses to tumors and possibly to virally infected nonhematopoietic cells, as well as in the establishment of peripheral tolerance 44. The mechanism of antigen acquisition and the cells involved in in vivo presentation in these circumstances are poorly understood. Uptake of apoptotic cells by phagocytic dendritic cells has been suggested as a key event 22, but recent data favor the activation of dendritic cells by material from necrotic cells 45, followed by efficient antigen presentation of released material by MHC class I molecules 2246. The loss of HSP/protein complexes from cells dying a necrotic death could be readily imagined to lead to antigen delivery via the processing pathways described here, in agreement with the proposal of Melcher et al. 47. Some antigen-associated HSP might also be released from viable infected or transformed cells due to saturation of the KDEL-retrieval pathway 48 after the HSP upregulation that results from stress due to microbial invasion or the poor oxygenation of growing tumors. In these cases, the complexes could contribute to an “early warning” system that promotes T cell activation by professional APCs that have efficiently bound them through surface receptors and converted them into peptide/MHC molecule ligands suitable for T cell recognition.
Finally, from a cell biology point of view, we are left with trying to understand how HSP/antigen complexes or the antigenic cargo of HSP molecules move across endosomal or plasma membranes into the cytosol. The only described pathway across such membranes for normal cellular proteins is in the opposite direction and involves lysosomes 49. Whether the same pathway can operate in reverse or whether another transport pathway remains to be discovered poses an intriguing question.
The authors wish to thank Dr. Jon Yewdell for his very helpful suggestions during this study and the preparation of this manuscript, as well as Dr. Owen Schwartz of the National Institute of Allergy and Infectious Diseases Confocal Microscope Facility for his help in obtaining the images used in this report.
A.N. Houghton was supported in part by a grant from Swim-Across-America and from the National Cancer Institute.
Abbreviations used in this paper: ER, endoplasmic reticulum; HSP, heat shock protein; TAP, transporter associated with antigen processing.
M. Mayhew's present address is Mojave Therapeutics, Inc., Tarrytown, NY 10591.