Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1975 Jan 1;64(1):75–88. doi: 10.1083/jcb.64.1.75

New immunolatex spheres: visual markers of antigens on lymphocytes for scanning electron microscopy

PMCID: PMC2109479  PMID: 803228

Abstract

New immunochemical reagents consisting of antibodies bound to small latex spheres were used as visual markers for the detection and localization of cell surface antigens by scanning electron microscopy. Cross-linked latex spheres of various sizes from 300 to 3,4000 A in diameter were synthesized by aqueous emulsion copolymerization of methacrylate derivatives containing hydroxyl and carboxyl functional groups. Proteins and other molecules containing primary amino groups were covalently bonded to the acrylic spheres under a variety of mild conditions by the aqueous carbodiimide, cyanogen bromide, and glutaraldehyde methods. For use in the indirect immunochemical-labeling technique, goat antibodies directed against rabbit immunoglobulins were bonded to the spheres. These immunolatex reagents were shown to bind only to cells (red blood and lymphocytes) which had previously been sensitized with rabbit antibodies against cell surface antigens. Mouse spleen lymphocytes with exposed immunoglobulins on their surface (B cells) were labeled with these spheres and distinguished from unlabeled or T lymphocytes by scanning electron microscopy. The distribution of Ig receptors on lymphocytes was also studied using the spheres as visual markers. When lymphocytes were fixed with glutaraldehyde and subsequently labeled with the immunolatex reagents, a random distribution was observed by scanning electron microscopy; a patchy distribution was observed when unfixed lymphocytes were used. These results are consistent with studies using ferritin-labeled antibodies (S. De Petris and M. Raff. 1973. Nature [Lond.]. 241:257.) and support the view that Ig receptors on lymphocytes undergo translational diffusion. In addition to serving as visual markers for scanning electron microscopy, these latex spheres tagged with fluorescent or radioactive molecules have applications as highly sensitive markers for fluorescent microscopy and as reagents for quantitative studies of cell surface antigens and other receptors.

Full Text

The Full Text of this article is available as a PDF (2.8 MB).

Selected References

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

  1. Aoki T., Boyse E. A., Old L. J., De Harven E., Hämmerling U., Wood H. A. G (Gross) and H-2 cell-surface antigens: location on Gross leukemia cells by electron microscopy with visually labeled antibody. Proc Natl Acad Sci U S A. 1970 Mar;65(3):569–576. doi: 10.1073/pnas.65.3.569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cuatrecasas P. Protein purification by affinity chromatography. Derivatizations of agarose and polyacrylamide beads. J Biol Chem. 1970 Jun;245(12):3059–3065. [PubMed] [Google Scholar]
  3. De Saussure V. A., Dandliker W. B. Ultracentrifuge studies on the effects of thiocyanate ion on antigen--antibody systems. Immunochemistry. 1969 Jan;6(1):77–83. doi: 10.1016/0019-2791(69)90180-3. [DOI] [PubMed] [Google Scholar]
  4. Froland S. S., Natvig J. B. Identification of three different human lymphocyte populations by surface markers. Transplant Rev. 1973;16:114–162. doi: 10.1111/j.1600-065x.1973.tb00119.x. [DOI] [PubMed] [Google Scholar]
  5. GOODFRIEND T. L., LEVINE L., FASMAN G. D. ANTIBODIES TO BRADYKININ AND ANGIOTENSIN: A USE OF CARBODIIMIDES IN IMMUNOLOGY. Science. 1964 Jun 12;144(3624):1344–1346. doi: 10.1126/science.144.3624.1344. [DOI] [PubMed] [Google Scholar]
  6. Karnovsky M. J., Unanue E. R., Leventhal M. Ligand-induced movement of lymphocyte membrane macromolecules. II. Mapping of surface moieties. J Exp Med. 1972 Oct 1;136(4):907–930. doi: 10.1084/jem.136.4.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lin P. S., Wallach D. F., Tsai S. Temperature-induced variations in the surface topology of cultured lymphocytes are revealed by scanning electron microscopy. Proc Natl Acad Sci U S A. 1973 Sep;70(9):2492–2496. doi: 10.1073/pnas.70.9.2492. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. MILGROM F., GOLDSTEIN R. Agglutination of sensitized red blood cells by latex particles. Vox Sang. 1962;7:86–88. doi: 10.1111/j.1423-0410.1962.tb03232.x. [DOI] [PubMed] [Google Scholar]
  9. Malin S. F., Edwards J. R. Detection of hepatitis associated antigen by latex agglutination. Nat New Biol. 1972 Feb 9;235(58):182–182. doi: 10.1038/newbio235182a0. [DOI] [PubMed] [Google Scholar]
  10. Meller S. M., Coppe M. R., Ito S., Waterman R. E. Transmission electron microscopy of critical point dried tissue after observation in the scanning electron microscope. Anat Rec. 1973 Jun;176(2):245–252. doi: 10.1002/ar.1091760210. [DOI] [PubMed] [Google Scholar]
  11. Otto H., Takamiya H., Vogt A. A two-stage method for cross-linking antibody globulin to ferritin by glutaraldehyde. Comparison between the one-stage and the two-stage method. J Immunol Methods. 1973 Oct;3(2):137–145. doi: 10.1016/0022-1759(73)90029-x. [DOI] [PubMed] [Google Scholar]
  12. Pernis B., Forni L., Amante L. Immunoglobulin spots on the surface of rabbit lymphocytes. J Exp Med. 1970 Nov;132(5):1001–1018. doi: 10.1084/jem.132.5.1001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Polliack A., Lampen N., Clarkson B. D., De Harven E., Bentwich Z., Siegal F. P., Kunkel H. G. Identification of human B and T lymphocytes by scanning electron microscopy. J Exp Med. 1973 Sep 1;138(3):607–624. doi: 10.1084/jem.138.3.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Rabellino E., Colon S., Grey H. M., Unanue E. R. Immunoglobulins on the surface of lymphocytes. I. Distribution and quantitation. J Exp Med. 1971 Jan 1;133(1):156–167. doi: 10.1084/jem.133.1.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Raff M. C., Sternberg M., Taylor R. B. Immunoglobulin determinants on the surface of mouse lymphoid cells. Nature. 1970 Feb 7;225(5232):553–554. doi: 10.1038/225553a0. [DOI] [PubMed] [Google Scholar]
  16. Singer S. J., Nicolson G. L. The fluid mosaic model of the structure of cell membranes. Science. 1972 Feb 18;175(4023):720–731. doi: 10.1126/science.175.4023.720. [DOI] [PubMed] [Google Scholar]
  17. Truffa-Bachi P., Wofsy L. Specific separation of cells on affinity columns. Proc Natl Acad Sci U S A. 1970 Jul;66(3):685–692. doi: 10.1073/pnas.66.3.685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Unanue E. R., Perkins W. D., Karnovsky M. J. Ligand-induced movement of lymphocyte membrane macromolecules. I. Analysis by immunofluorescence and ultrastructural radioautography. J Exp Med. 1972 Oct 1;136(4):885–906. doi: 10.1084/jem.136.4.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. WESTERMAN M. P., PIERCE L. E., JENSEN W. N. A direct method for the quantitative measurement of red cell dimensions. J Lab Clin Med. 1961 May;57:819–824. [PubMed] [Google Scholar]
  20. de Petris S., Raff M. C. Normal distribution, patching and capping of lymphocyte surface immunoglobulin studied by electron microscopy. Nat New Biol. 1973 Feb 28;241(113):257–259. doi: 10.1038/newbio241257a0. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES