ABSTRACT
The functional maintenance of the vascular endothelial cell barrier depends on different
homo- and heterotypic adhesion systems involving tight junctions, junctional adhesion
proteins, and cadherins. Upon inflammatory responses, vessel wall-dependent adhesion
and transmigration of leukocytes involves the subtle orchestration of intercellular
adhesion receptors and their counter-ligands on each cell type. Following tissue injury,
the hemostatic/wound-healing process relies on various cell-associated adhesion receptors
(particularly integrins) on platelets and vascular cells as well as on extracellular
matrix (ECM) proteins to warrant sealing of the wound. In particular, integrin-binding
ECM adhesion molecules mediate firm anchorage as well as cellular motility in cooperation
with pericellular proteolytic systems. Accumulating evidence indicates that such cell-anchored
and ECM adhesion proteins, which are crucial in vascular defense processes, are also
expressed in the testicular epithelium and in gametes to mediate the timely events
of spermatid movement during spermatogenesis in the testis and to contribute to the
various phases of the fertilization process, culminating in sperm-oocyte fusion, respectively.
We explore the multifunctional roles of junctional adhesion molecules, nectins, integrins,
ECM proteins, and others beyond their role in defense and hemostasis as important
contributors in spermatogenesis and sperm function.
KEYWORDS
Spermatogenesis - gamete fusion - junctional adhesion molecules - integrins - extracellular
matrix
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Klaus T PreissnerPh.D.
Department of Biochemistry, Medical School, Justus-Liebig-University
Friedrichstrasse 24, D-35392 Giessen, Germany
Email: klaus.t.preissner@biochemie.med.uni-giessen.de