Table 3.
Seminal plasma proteins in spermatozoa protection, transport and interaction with the female reproductive tract
Proteins involved | Site of Action | Mechanism of action | Reference |
---|---|---|---|
FOXP3 | Uterine regulatory T cells | Immunosuppression and improved tolerance towards paternal antigens | [96–98] |
GM-CSF | Embryo | Blastocyst stage development | [72] |
IL-6 | Embryo | Protection from apoptosis by secreting anti-apoptotic micro RNAs | [72] |
LIF | Inner cell mass | Blastocyst development | [72] |
IGF-1 | Germ cells | Maturation of spermatozoa | [27, 28] |
α2-macroglobulin | Germ cells | Progressive motility | [27, 28] |
Enkephalin | Sperm cells | Sperm motility | [27, 28] |
VEGF, MMPs | Endometrium | Embryo implantation | [40, 99] |
TGF-β, PGE | Female reproductive epithelial tissues | Inflammatory signaling response | [40, 99] |
GM-CSF, IL-1A, IL-6, IL-8, MCP-1 (CCL2), MIP3A (CCL20) | Female epithelial layers and deeper stromal tissues | Immediate and rapid influx of inflammation to cause fertilization | [5, 65, 74, 99] |
Several studies showing the importance of seminal plasma proteins in the regulation of male and female reproductive mechanisms. However, some of the studies were conducted with animal samples and still need validation by studies with human samples
Abbreviations: FOXP3 forkhead box P3, GM-CSF granulocyte-macrophage colony stimulating factor, IL interleukin, LIF leukemia inhibitory factor, IGF insulin like growth gactor, VEGF vascular endothelial growth factor, MMPs matrix metalloproteinases, TGF-β transforming growth factor beta, PGE prostaglandin E synthase, MCP-1 monocyte chemoattractant protein-1, MIP-3A macrophage inflammatory protein 3, CCL chemokine ligand