Skip to main content
British Journal of Cancer logoLink to British Journal of Cancer
. 1999 May;80(5-6):639–649. doi: 10.1038/sj.bjc.6690405

Biosynthesis of HLA-C heavy chains in melanoma cells with multiple defects in the expression of HLA-A, -B, -C molecules

A Martayan 1, R Fraioli 1, E Giorda 1, A Setini 1, G Ciccarelli 1, L Delfino 2, G B Ferrara 2, P Giacomini 1
PMCID: PMC2362293  PMID: 10360639

Abstract

Recent investigations have shown that malignant transformation may down-regulate the expression of class I HLA molecules, β2-microglobulin (β2m) and members of the antigen-processing machinery. In the present study, we HLA-genotyped and identified at a biochemical level the three (HLA-A25, -B8, -Cw7) class I alleles expressed by the previously described [D'Urso CM et al (1992) J Clin Invest 87: 284–292] β2m-defective human melanoma FO-1 cell line and tested their ability to interact with calnexin, calreticulin and the TAP (transporter associated with antigen processing) complex. All these alleles were found to bind calnexin, but not calreticulin or the poorly expressed TAP complex, both in parental and β2m-transfected FO-1 cells, demonstrating a complex defect of class I expression in FO-1 cells. In these conditions, Cw7 heavy chains interacted with calnexin more strongly than A25 and B8, and preferentially accumulated in the endoplasmic reticulum, in both a calnexin-associated and a calnexin-free form. In addition, they could be transported to the cell surface at low levels even in the absence of β2m, without undergoing terminal glycosylation. These results establish a parallel between HLA-C and the murine Db and Ld molecules which have been found to be surface expressed and functional in β2m-defective cells. They also demonstrate distinctive features of HLA-C molecules. We propose that the accumulation of several assembly intermediates of HLA-C might favour the binding of peptide antigens not readily bound by HLA-A and -B molecules in neoplastic cells with suboptimal class I expression. © 1999 Cancer Research Campaign

Keywords: HLA-C, β2-microglobulin, calnexin, calreticulin, TAP, melanoma

Full Text

The Full Text of this article is available as a PDF (553.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allen H., Fraser J., Flyer D., Calvin S., Flavell R. Beta 2-microglobulin is not required for cell surface expression of the murine class I histocompatibility antigen H-2Db or of a truncated H-2Db. Proc Natl Acad Sci U S A. 1986 Oct;83(19):7447–7451. doi: 10.1073/pnas.83.19.7447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bicknell D. C., Rowan A., Bodmer W. F. Beta 2-microglobulin gene mutations: a study of established colorectal cell lines and fresh tumors. Proc Natl Acad Sci U S A. 1994 May 24;91(11):4751–4755. doi: 10.1073/pnas.91.11.4751. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cook J. R., Solheim J. C., Connolly J. M., Hansen T. H. Induction of peptide-specific CD8+ CTL clones in beta 2-microglobulin-deficient mice. J Immunol. 1995 Jan 1;154(1):47–57. [PubMed] [Google Scholar]
  4. D'Urso C. M., Wang Z. G., Cao Y., Tatake R., Zeff R. A., Ferrone S. Lack of HLA class I antigen expression by cultured melanoma cells FO-1 due to a defect in B2m gene expression. J Clin Invest. 1991 Jan;87(1):284–292. doi: 10.1172/JCI114984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Degen E., Williams D. B. Participation of a novel 88-kD protein in the biogenesis of murine class I histocompatibility molecules. J Cell Biol. 1991 Mar;112(6):1099–1115. doi: 10.1083/jcb.112.6.1099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Elliott T. How do peptides associate with MHC class I molecules? Immunol Today. 1991 Nov;12(11):386–388. doi: 10.1016/0167-5699(91)90134-f. [DOI] [PubMed] [Google Scholar]
  7. Elliott T. How does TAP associate with MHC class I molecules? Immunol Today. 1997 Aug;18(8):375–379. doi: 10.1016/s0167-5699(97)01097-9. [DOI] [PubMed] [Google Scholar]
  8. Garrido F., Cabrera T., Concha A., Glew S., Ruiz-Cabello F., Stern P. L. Natural history of HLA expression during tumour development. Immunol Today. 1993 Oct;14(10):491–499. doi: 10.1016/0167-5699(93)90264-L. [DOI] [PubMed] [Google Scholar]
  9. Gattoni-Celli S., Kirsch K., Timpane R., Isselbacher K. J. Beta 2-microglobulin gene is mutated in a human colon cancer cell line (HCT) deficient in the expression of HLA class I antigens on the cell surface. Cancer Res. 1992 Mar 1;52(5):1201–1204. [PubMed] [Google Scholar]
  10. Giacomini P., Beretta A., Nicotra M. R., Ciccarelli G., Martayan A., Cerboni C., Lopalco L., Bini D., Delfino L., Ferrara G. B. HLA-C heavy chains free of beta2-microglobulin: distribution in normal tissues and neoplastic lesions of non-lymphoid origin and interferon-gamma responsiveness. Tissue Antigens. 1997 Dec;50(6):555–566. doi: 10.1111/j.1399-0039.1997.tb02913.x. [DOI] [PubMed] [Google Scholar]
  11. Hajek-Rosenmayr A., Jungl L., Stammler M., Kirnbauer M. HLA-C locus antigens seen by one-dimensional isoelectric focusing: definition of the so far known HLA-C specificities and of two subtypes. Hum Immunol. 1989 Dec;26(4):227–236. doi: 10.1016/0198-8859(89)90001-3. [DOI] [PubMed] [Google Scholar]
  12. Hansen T. H., Lee D. R. Mechanism of class I assembly with beta 2 microglobulin and loading with peptide. Adv Immunol. 1997;64:105–137. doi: 10.1016/s0065-2776(08)60888-3. [DOI] [PubMed] [Google Scholar]
  13. Hansen T. H., Myers N. B., Lee D. R. Studies of two antigenic forms of Ld with disparate beta 2-microglobulin (beta 2m) associations suggest that beta 2m facilitate the folding of the alpha 1 and alpha 2 domains during de novo synthesis. J Immunol. 1988 May 15;140(10):3522–3527. [PubMed] [Google Scholar]
  14. Lehmann-Grube F., Dralle H., Utermöhlen O., Löhler J. MHC class I molecule-restricted presentation of viral antigen in beta 2-microglobulin-deficient mice. J Immunol. 1994 Jul 15;153(2):595–603. [PubMed] [Google Scholar]
  15. Long E. O., Wagtmann N. Natural killer cell receptors. Curr Opin Immunol. 1997 Jun;9(3):344–350. doi: 10.1016/s0952-7915(97)80080-5. [DOI] [PubMed] [Google Scholar]
  16. Machold R. P., Andrée S., Van Kaer L., Ljunggren H. G., Ploegh H. L. Peptide influences the folding and intracellular transport of free major histocompatibility complex class I heavy chains. J Exp Med. 1995 Mar 1;181(3):1111–1122. doi: 10.1084/jem.181.3.1111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Markwell M. A., Fox C. F. Surface-specific iodination of membrane proteins of viruses and eucaryotic cells using 1,3,4,6-tetrachloro-3alpha,6alpha-diphenylglycoluril. Biochemistry. 1978 Oct 31;17(22):4807–4817. doi: 10.1021/bi00615a031. [DOI] [PubMed] [Google Scholar]
  18. Martayan A., Fiscella M., Setini A., Ciccarelli G., Gambari R., Feriotto G., Beretta A., Siccardi A. G., Appella E., Giacomini P. Conformation and surface expression of free HLA-CW1 heavy chains in the absence of beta 2-microglobulin. Hum Immunol. 1997 Mar;53(1):23–33. doi: 10.1016/S0198-8859(96)00256-X. [DOI] [PubMed] [Google Scholar]
  19. Neefjes J. J., Breur-Vriesendorp B. S., van Seventer G. A., Iványi P., Ploegh H. L. An improved biochemical method for the analysis of HLA-class I antigens. Definition of new HLA-class I subtypes. Hum Immunol. 1986 Jun;16(2):169–181. doi: 10.1016/0198-8859(86)90046-7. [DOI] [PubMed] [Google Scholar]
  20. Neefjes J. J., Ploegh H. L. Allele and locus-specific differences in cell surface expression and the association of HLA class I heavy chain with beta 2-microglobulin: differential effects of inhibition of glycosylation on class I subunit association. Eur J Immunol. 1988 May;18(5):801–810. doi: 10.1002/eji.1830180522. [DOI] [PubMed] [Google Scholar]
  21. Neisig A., Melief C. J., Neefjes J. Reduced cell surface expression of HLA-C molecules correlates with restricted peptide binding and stable TAP interaction. J Immunol. 1998 Jan 1;160(1):171–179. [PubMed] [Google Scholar]
  22. Ortmann B., Copeman J., Lehner P. J., Sadasivan B., Herberg J. A., Grandea A. G., Riddell S. R., Tampé R., Spies T., Trowsdale J. A critical role for tapasin in the assembly and function of multimeric MHC class I-TAP complexes. Science. 1997 Aug 29;277(5330):1306–1309. doi: 10.1126/science.277.5330.1306. [DOI] [PubMed] [Google Scholar]
  23. Parham P., Barnstable C. J., Bodmer W. F. Use of a monoclonal antibody (W6/32) in structural studies of HLA-A,B,C, antigens. J Immunol. 1979 Jul;123(1):342–349. [PubMed] [Google Scholar]
  24. Pellegrino M. A., Ng A. K., Russo C., Ferrone S. Heterogeneous distribution of the determinants defined by monoclonal antibodies on HLA-A and B antigens bearing molecules. Transplantation. 1982 Jul;34(1):18–23. doi: 10.1097/00007890-198207000-00004. [DOI] [PubMed] [Google Scholar]
  25. Pera C., Delfino L., Morabito A., Longo A., Johnston-Dow L., White C. B., Colonna M., Ferrara G. B. HLA-A typing: comparison between serology, the amplification refractory mutation system with polymerase chain reaction and sequencing. Tissue Antigens. 1997 Oct;50(4):372–379. doi: 10.1111/j.1399-0039.1997.tb02890.x. [DOI] [PubMed] [Google Scholar]
  26. Porgador A., Mandelboim O., Restifo N. P., Strominger J. L. Natural killer cell lines kill autologous beta2-microglobulin-deficient melanoma cells: implications for cancer immunotherapy. Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13140–13145. doi: 10.1073/pnas.94.24.13140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Potter T. A., Boyer C., Verhulst A. M., Golstein P., Rajan T. V. Expression of H-2Db on the cell surface in the absence of detectable beta 2 microglobulin. J Exp Med. 1984 Jul 1;160(1):317–322. doi: 10.1084/jem.160.1.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Prasad V. K., Yang S. Y. Allele assignment for HLA-A, -B, and -C genes to the Tenth International Histocompatibility Workshop cell lines. Tissue Antigens. 1996 Jun;47(6):538–546. doi: 10.1111/j.1399-0039.1996.tb02596.x. [DOI] [PubMed] [Google Scholar]
  29. Rajagopalan S., Brenner M. B. Calnexin retains unassembled major histocompatibility complex class I free heavy chains in the endoplasmic reticulum. J Exp Med. 1994 Jul 1;180(1):407–412. doi: 10.1084/jem.180.1.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Sadasivan B., Lehner P. J., Ortmann B., Spies T., Cresswell P. Roles for calreticulin and a novel glycoprotein, tapasin, in the interaction of MHC class I molecules with TAP. Immunity. 1996 Aug;5(2):103–114. doi: 10.1016/s1074-7613(00)80487-2. [DOI] [PubMed] [Google Scholar]
  31. Salter R. D., Cresswell P. Impaired assembly and transport of HLA-A and -B antigens in a mutant TxB cell hybrid. EMBO J. 1986 May;5(5):943–949. doi: 10.1002/j.1460-2075.1986.tb04307.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Seliger B., Maeurer M. J., Ferrone S. TAP off--tumors on. Immunol Today. 1997 Jun;18(6):292–299. doi: 10.1016/s0167-5699(97)01052-9. [DOI] [PubMed] [Google Scholar]
  33. Setini A., Beretta A., De Santis C., Meneveri R., Martayan A., Mazzilli M. C., Appella E., Siccardi A. G., Natali P. G., Giacomini P. Distinctive features of the alpha 1-domain alpha helix of HLA-C heavy chains free of beta 2-microglobulin. Hum Immunol. 1996 Apr;46(2):69–81. doi: 10.1016/0198-8859(96)00011-0. [DOI] [PubMed] [Google Scholar]
  34. Shimizu Y., DeMars R. Production of human cells expressing individual transferred HLA-A,-B,-C genes using an HLA-A,-B,-C null human cell line. J Immunol. 1989 May 1;142(9):3320–3328. [PubMed] [Google Scholar]
  35. Smith J. D., Myers N. B., Gorka J., Hansen T. H. Model for the in vivo assembly of nascent Ld class I molecules and for the expression of unfolded Ld molecules at the cell surface. J Exp Med. 1993 Dec 1;178(6):2035–2046. doi: 10.1084/jem.178.6.2035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Solheim J. C., Carreno B. M., Hansen T. H. Are transporter associated with antigen processing (TAP) and tapasin class I MHC chaperones? J Immunol. 1997 Jan 15;158(2):541–543. [PubMed] [Google Scholar]
  37. Solheim J. C., Harris M. R., Kindle C. S., Hansen T. H. Prominence of beta 2-microglobulin, class I heavy chain conformation, and tapasin in the interactions of class I heavy chain with calreticulin and the transporter associated with antigen processing. J Immunol. 1997 Mar 1;158(5):2236–2241. [PubMed] [Google Scholar]
  38. Stam N. J., Spits H., Ploegh H. L. Monoclonal antibodies raised against denatured HLA-B locus heavy chains permit biochemical characterization of certain HLA-C locus products. J Immunol. 1986 Oct 1;137(7):2299–2306. [PubMed] [Google Scholar]
  39. Wang Z., Arienti F., Parmiani G., Ferrone S. Induction and functional characterization of beta2-microglobulin (beta2-mu)-free HLA class I heavy chains expressed by beta2-mu-deficient human FO-1 melanoma cells. Eur J Immunol. 1998 Sep;28(9):2817–2826. doi: 10.1002/(SICI)1521-4141(199809)28:09<2817::AID-IMMU2817>3.0.CO;2-M. [DOI] [PubMed] [Google Scholar]
  40. Wang Z., Cao Y., Albino A. P., Zeff R. A., Houghton A., Ferrone S. Lack of HLA class I antigen expression by melanoma cells SK-MEL-33 caused by a reading frameshift in beta 2-microglobulin messenger RNA. J Clin Invest. 1993 Feb;91(2):684–692. doi: 10.1172/JCI116249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Wang Z., Margulies L., Hicklin D. J., Ferrone S. Molecular and functional phenotypes of melanoma cells with abnormalities in HLA class I antigen expression. Tissue Antigens. 1996 May;47(5):382–390. doi: 10.1111/j.1399-0039.1996.tb02573.x. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES