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The JAM Family of Molecules and Their Role in the Regulation of Physiological and Pathological Processes
Insights
Junctional adhesion molecules (JAMs) regulate various physiological processes and are implicated in numerous diseases, including cardiovascular conditions, nervous system disorders, and cancer. Peptide geroprotectors may influence JAMs expression through epigenetic mechanisms.
Area of Science:
- Cell adhesion biology
- Molecular medicine
- Immunology
Background:
- Junctional adhesion molecules (JAMs) are a family of cell adhesion proteins crucial for maintaining tissue integrity and regulating cell-cell interactions.
- Dysregulation of JAMs is associated with various pathological conditions, highlighting their significance in disease pathogenesis.
Purpose of the Study:
- To review the diverse functions of JAMs family members.
- To elucidate the role of specific JAMs (JAM-A, JAM-B, JAM-C) in pathological processes.
- To explore potential therapeutic implications, including the role of peptide geroprotectors.
Main Methods:
- Literature review of JAMs functions and roles in diseases.
- Analysis of existing data on JAMs involvement in nervous system, cardiovascular diseases, cancer, and inflammatory conditions.
- Discussion of potential epigenetic regulation mechanisms.
Main Results:
- JAM-C and JAM-A influence platelet and leukocyte adhesion, impacting hemostasis and migration.
- JAM-A is linked to cognitive impairment in HIV and breast cancer.
- JAM-B suppresses tumor growth and, along with JAM-C, inhibits glioma invasion.
- JAMs are involved in hypertension, atherosclerosis, cardiac abnormalities, and corneal angiogenesis.
- JAM-C plays a role in retinal photoreceptor development.
Conclusions:
- JAMs are critical regulators of diverse physiological and pathological processes.
- Aberrant JAMs expression contributes to a wide spectrum of diseases.
- Epigenetic mechanisms, potentially modulated by peptide geroprotectors, may regulate JAMs expression, offering novel therapeutic avenues.
Abstract:
The review covers the main functions of the family of adhesion molecules JAMs (Junctional adhesion molecules). This review provides information about the role of the molecules JAM-AH, JAM-BH and JAM-CF in the occurrence of pathological conditions, including diseases of the nervous and cardiovascular systems, atherosclerosis, thrombosis and malignant growth. A molecule JAM-C and JAM-C directly affect platelet’s adhesion to endothelial and dendritic cells, neutrophils, and other types of leukocytes, which makes their involvement in the regulation of hemostasis, and migration processes. JAM-A has an effect on the inflammatory response, leading to impaired cognitive function in HIV infection. JAM-B is involved in suppression of tumor growth in patients with Down syndrome. It is described the role of molecule JAM-A and JAM-C in the pathogenesis of hypertension, hypertensive crisis, atherosclerosis, cardiac abnormalities in the syndrome of Jacobson. Molecules JAM-B and JAM-C reduce the growth and invasion of human gliomas, and JAM-A has static effect against breast cancer. JAM-A molecule, JAM-B and JAM-C are involved in the development of inflammatory reactions and pathological neoangiogenesis in the cornea. The molecule JAM-C is involved in differentiation and polarization photoreceptors of the retina. The review provides own data of the authors, suggests the presence of epigenetic mechanisms of regulation of expression of the family of molecules JAMs, carried out with the direct participation of peptide geroprotectors.
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