55 research outputs found
Partial characterization of Ia antigens from murine lymphoid cells
Congenic anti-Ia antisera were used to bind radiolabelled Ia antigens from cells of various strains of mice of known H-2 haplotype. The results indicate that Ia antigens are proteins of molecular weight 30,000 to 35,000 daltons. The Ia antigens are distinct from known H-2 antigens as judged by independent immunoprecipitation as well as by molecular weight. Ia antigens are synthesized by, and are present on the surface of lymphoid cells as evidenced by incorporation studies using 3 H-leucine and enzymatic radioiodination of cells, respectively. Tissue distribution of cell surface Ia suggests that Ia antigens are on B cells. Ia antigens were detected in the incubation media of 3 H-leucine labeled splenocytes suggesting that antigens may be secreted.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/46728/1/251_2005_Article_BF01564048.pd
Adhesion molecules as targets for cancer therapy
Adhesion molecules mediate cell-cell and
cell-matrix interactions and are essential for numerous
physiological and pathological processes. Recent
evidence from many laboratories suggests that adhesion
molecules play an important role in tumor progression
and may promote tumor growth and organ-specific
metastasis. Certain adhesion molecules may also
function as tumor suppressors. In this review, we
describe current concepts concerning the role of the
adhesion molecules in the pathogenesis of cancer and the
development of therapeutic approaches which make use
of this information. Hence, by preventing tumor cells
from interacting with each other or with their microenvironment,
tumor growth and metastasis can be
suppressed. The feasibility of using anti-adhesion
strategies to treat cancer has been demonstrated in many
animal models. Thus, monoclonal antibodies (MAbs)
against adhesion molecules, synthetic peptidic and
nonpeptidic analogues of the recognition sequences on
their receptors, soluble adhesion molecules and antisense
oligonucleotides can inhibit tumor growth and gene
therapy can restore the functions of altered tumorsuppressive
adhesion molecules
DIFFERENTIAL RADIOLABELLING OF LYMPHOCYTE MEMBRANE ALLOANTIGENS AND IMMUNOGLOBULINS: VARIATION OF H 2
Stochastic models of receptor oligomerization by bivalent ligand
In this paper, we develop stochastic models of receptor binding by a bivalent ligand. A detailed kinetic study allows us to analyse the role of cross-linking in cell activation by receptor oligomerization. We show how oligomer formation could act to buffer intracellular signalling against stochastic fluctuations. In addition, we put forward the hypothesis that formation of long linear oligomers increases the range of ligand concentration to which the cell is responsive, whereas formation of closed oligomers increases ligand concentration specificity. Thus, different physiological functions requiring different degrees of specificity to ligand concentration would favour formation of oligomers with different lengths and geometries. Furthermore, provided that ligand concentration specificity is taken as a design principle, our model enables us to estimate parameters, such as the minimum proportion of receptors, that must engage in oligomer formation in order to trigger a cellular response
HEAVY CHAINS OF MURINE SPLENOCYTE MEMBRANE IMMUNOGLOBULINS: A COMPARISON WITH THE HEAVY CHAINS OF HUMAN AND TOAD SERUM IMMUNOGLOBULINS
Amino Acid Sequence Analysis, Gene Construction, Cloning, and Expression of Gelonin, a Toxin Derived from Gelonium multiflorum
Iodination of Mono- and Heteroclonal Immunoglobulin G with Lactoperoxidase and Chloramine T
The Effect of Anti-Ia Antibody on Immunoglobulin-secreting Cells from Healthy Individuals and Myeloma Patients
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