It stimulates mitogenicity and chemotaxis of several cell types, and stimulates production of several matrix molecules. Some of the cellular responses manifest within minutes after PDGF receptor activation. PDGF stimulates rearrangement of actin filaments that comprise the major cytoskeletal components in eukaryotic cells. Alteration of actin polymerization has been implicated in various cell responses, including proliferation Selleckchem Adriamycin and motility. Depolymerization of actin filaments impairs the morphology, motility and division of most cells. Coordinated movement is a fundamental cellular process essential for keratinocytes and fibroblasts during wound healing and for the

extravasation of immune cells during inflammation [22]. In a previous study [6], we speculated that anti-PDGF activity may partly explain reports of SGE from I. scapularis affecting cellular adherence and angiogenesis [27, 28]. We also observed a correlation between anti-PDGF activity and the inhibition in proliferation of glioma, PS

and NIH-3T3 cells in vitro (Table 2). The major cellular component of the epidermis is the keratinocytes [29]; the dermal layer contains mainly fibroblasts. Here, we demonstrate the effect of SGE of adult H. excavatum ticks on human skin keratinocytes HaCaT and mouse fibroblasts NIH-3T3, as representatives of two basal skin cell types. The proliferation of HaCaT cells was inhibited to a greater MK-2206 molecular weight degree than NIH-3T3 fibroblasts by H. excavatum SGE. The highest inhibition of proliferation of both cell lines was obtained by SGE prepared from 7-day-fed females, whereas treatment of cells with SGE of 3-day-fed females had comparatively little effect. Moreover, the shape of both HaCaT and NIH-3T3 cell lines was altered by treatment with SGE from females

feeding for 7 days but not for 3 days. Rucaparib mouse This alteration was associated also with loss of cell adhesion to the microtitre plate. Comparison of the treatment of cells with H. excavatum SGE prepared from early phase tick feeding showed that even though the samples contained molecules binding PDGF they did not have a visible effect on actin microfilaments, especially when compared with the pronounced effect of SGE from females in the late phase of engorgement. Such a robust effect on the actin cytoskeleton was not seen even when we used fourfold SGE equivalents of 3-day-fed ticks that we estimate should have equivalent potency in anti-PDGF activity to 7-day-fed females. Thus, it seems that female ixodid ticks with long mouthparts produce, in their salivary glands, additional factor(s) to ensure their invisibility and protect them against attack by the host immune system during the massive blood uptake in the terminal phase of feeding. For example, metalloproteases may play a role in manipulating the wound-healing response as they appear to be abundantly expressed in the salivary glands of Amblyomma and Ixodes species, and they affect cell proliferation and angiogenesis [28, 30].