Dr. Peter D'Adamo/ The Blood Type Diets
dadamowiki

A wikipedia of Dr. D'Adamo's research



Cell Adhesion Molecules (CAMs)


Lectinology

See Also

Description

Cell Adhesion Molecules (CAMs) are proteins located on the cell surface involved with the binding with other cells or with the extracellular matrix (ECM) in the process called cell adhesion.

These proteins are typically transmembrane receptors and are composed of three domains: an intracellular domain that interacts with the cytoskeleton, a transmembrane domain and an extracellular domain that interacts either with other CAMs of the same kind (homophilic binding) or with other CAMs or the extracellular matrix (heterophilic binding).

Families of CAMs

Most of the CAMs belong to 4 protein families: Ig (immunoglobulin) superfamily (IgSF CAMs), the integrins, the cadherins and the selectins.

IgSF CAMs

Immunoglobulin SuperFamily CAMs (IgSF CAMs) are either homophilic or heterophilic and bind integrins or different IgSF CAMs. Here is a list of some molecules of this family:

Selectins

The selectins are a family of heterophilic CAMs that bind fucosylated carbohydrates, e.g. mucins . They are dependent on divalent cations. The most important family members are E-selectins (endothelial), L-selectins (leukocyte) and P-selectins (platelet). An example of a member of this family is the P-selectin glycoprotein ligand-1 (PSGL-1).

Integrins

The integrins are a family of heterophilic CAMs that bind IgSF CAMs or the extracellular matrix. They are heterodimers, consisting in two non-covalently linked subunits, called alpha and beta. 24 different alpha subunits are known that can link in many different combinations with the 9 different beta subunits, however not all combinations are observed.

Cadherins

The cadherins are a family of homophilic CAMs, Calcium dependant. The most important members of this family are E-cadherins (epithelial), P-cadherins (placental) and N-cadherins (neural).

Pathology

Diabetes

In diabetes, glycation, tissue oxidation and endothelial function are all abnormal and predisposing to microvascular complications but interrelationships are complex with glycation appearing most direct.

Levels of soluble adhesion molecules vWf, E-selectin and VCAM are raised in Type 2 diabetes mellitus. In diabetic humans, elevated plasma von Willebrand Factor (vWF) has been interpreted as an indication of endothelial damage.

Endothelial activation and acute-phase reaction correlate with insulin resistance and obesity in type 2 diabetic patients obesity may induce endothelial activation or increased shedding of cell surface E-selectin that leads to subsequent increase in soluble E-selectin levels. High serum concentrations of E-selectin closely correlate with increased total fat volume.

Pharmacognacy of adhesion antagonism

Eupatorium purpureum
Feverfew (parthenolide)
Selenium
Astragalus
Carotenoids
Soy
Oligomeric proanthocyanidins (OPC's)
Vitamin E
Red Rice Yeast

Statins reduce E-selectin and ICAM. Red Rice Yeast (dihydromonacolin, monacolin I-VI, monacolin M, Monacolin K [very low]) may be an effective strategy in the management of diabetic complications.

Abstracts

The anti-inflammatory action of methotrexate is not mediated by lymphocyte apoptosis, but by the suppression of activation and adhesion molecules

Clin Immunol. 2005 Feb ;114:154-63

Andrew Johnston, Johann Eli Gudjonsson, Hekla Sigmundsdottir, Björn Runar Ludviksson, Helgi Valdimarsson

Low-dose methotrexate (MTX) is an established and highly effective treatment for severe psoriasis and rheumatoid arthritis; however, its mechanism of action remains unclear. We investigated the effects of low-dose MTX on antigen-stimulated peripheral blood mononuclear cells and explored through which cellular pathways these effects are mediated. We show that MTX caused a dose-dependent suppression of T cell activation and adhesion molecule expression, and this was not due to lymphocyte apoptosis. The suppression of intercellular adhesion molecule (ICAM)-1 was adenosine and folate-dependent, while MTX suppression of the skin-homing cutaneous lymphocyte-associated antigen (CLA) was adenosine-independent. The effect of MTX on CLA, but not ICAM-1, required the constant presence of MTX in cultures. Thus, the suppression of T cell activation and T cell adhesion molecule expression, rather than apoptosis, mediated in part by adenosine or polyglutamated MTX or both, are important mechanisms in the anti-inflammatory action of MTX.

The role of adhesion molecules in atherosclerosis




share on Facebook









The statements made on our websites have not been evaluated by the FDA (U.S. Food & Drug Administration). Our products and services are not intended to diagnose, cure or prevent any disease. If a condition persists, please contact your physician. Copyright © 2015-2026, Hoop-A-Joop, LLC, Inc. All Rights Reserved.