Spiniferaphonte, a new genus of Laophontidae (Copepoda: Harpacticoida), with notes on the occurrence of processes on the caudal rami

A new genus and species of Laophontidae, Spiniferaphonte ornata n. gen., n. sp., is described from the coast of Kenya. The new genus is closely related to Laophontina and Wellsiphontina as shown by the following synapomorphies: a denticulate operculum, a sexually dimorphic P4 exopod (reduced chaetotaxy of the ultimate segment in the male), and the absence of sexual dimorphism in the P2 and P3 endopods. The two-segmented exopod of PI and the presence of a seta on the endopodal part of the male P5 are plesiomorphies indicating that the new genus represents a separate lineage within this group. The proposal of the new genus Spiniferaphonte is supported by the following autapomorphies: three smooth setae on the female P5 exopod and a robust, dorsally bent, and strongly sclerotised caudal seta V. Within the Laophontidae, it is striking that the presence of distinct, thorn-like processes on the caudal rami is limited to interstitial genera. Distinct processes on the proximal segments of the antennule and a proximally thickened caudal seta V also appear to be associated with this interstitiality. These structures may play a role in the movement and the anchoring of the animals in their interstitial habitat

Two new genera of Laophontidae (Copepoda: Harpacticoida) without sexual dimorphism in the endopods of the swimming legs

Two new monospecific genera of the harpacticoid family Laophontidae T. Scott, 1905 are described here. Apistophonte wasiniensis gen. et sp. n. was found along the Kenyan coast and Propephonte duangitensis gen. et sp. n. along the northern coast of Papua New Guinea. They differ from most other laophontid genera in the absence of sexual dimorphism in the endopods of the swimming legs. At first sight, both new species resemble each other very closely in habitus, integumental ornamentation, chaetotaxy of the swimming legs and absence of sexual dimorphism in the endopods. However, the detailed characteristics of A1, maxilla and male P5 show that the species are not congeneric. The structure of the first antennular segment of Propephonte gen. n. suggests a close relationship with Peltidiphonte Gheerardyn and Fiers, 2006. The exact affinities of Apistophonte gen. n. however remain difficult to assess

Paralaophonte harpagone sp. n. (Copepoda: Harpacticoida), a laophontid with an extremely specialised maxilliped

Paralaophonte harpagone sp. n. is described from the coast of Kenya. The new species does not show any sexual dimorphism in the endopodite of P3 nor in the exopodites of P2 to P4. However, it is a true representative of the genus Peralaophonte by virtue of the typical sexually dimorphic P2 endopodite with its modified distal inner seta on the second endopodal segment. The most distinguishing feature of the new species is the robust, enlarged and specialised maxilliped, present in both sexes. This maxilliped is similar in robustness and position to the highly specialised maxilliped in the laophontid genus Namakosiramia Ho & Perkins, 1977 the two members of which live as ectoparasites on holothurians. We can only speculate whether the specialised maxilliped of Paralaophonte harpagone sp, n. is an adaptation to living in association with another invertebrate

Sex hormone-binding globulin regulation of androgen bioactivity in vivo : validation of the free hormone hypothesis

Sex hormone-binding globulin (SHBG) is the high-affinity binding protein for androgens and estrogens. According to the free hormone hypothesis, SHBG modulates the bioactivity of sex steroids by limiting their diffusion into target tissues. Still, the in vivo physiological role of circulating SHBG remains unclear, especially since mice and rats lack circulating SHBG post-natally. To test the free hormone hypothesis in vivo, we examined total and free sex steroid concentrations and bioactivity on target organs in mice expressing a human SHBG transgene. SHBG increased total androgen and estrogen concentrations via hypothalamic-pituitary feedback regulation and prolonged ligand half-life. Despite markedly raised total sex steroid concentrations, free testosterone was unaffected while sex steroid bioactivity on male and female reproductive organs was attenuated. This occurred via a liganddependent, genotype-independent mechanism according to in vitro seminal vesicle organ cultures. These results provide compelling support for the determination of free or bioavailable sex steroid concentrations in medicine, and clarify important comparative differences between translational mouse models and human endocrinology

Revision of the genus Tapholeon Wells, 1967 (Copepoda, Harpacticoida, Laophontidae)

To date, only two species are known in the laophontid genus Tapholeon Wells, 1967 (Copepoda, Harpacticoida). In the present contribution, a redescription of the type species T. ornatus Wells, 1967, based on the type material, is provided. Furthermore, two new species are described from the coast of Kenya, T. inconspicuus sp. nov. and T. tenuis sp. nov. Two species, formerly attributed to Asellopsis Brady and Robertson, 1873 (namely A. arenicola Chappuis, 1954 and A. chappuisius Krishnaswamy, 1957), are allocated to Tapholeon based on the absence of sexual dimorphism in the swimming legs P2-P4. The former of the two species is redescribed based on additional material from the Comoros. An updated generic diagnosis and a key to the six species of Tapholeon are included

FAN, a Novel WD-Repeat Protein, Couples the p55 TNF-Receptor to Neutral Sphingomyelinase

AbstractThe initiation of intracellular signaling events through the 55 kDa tumor necrosis factor–receptor (TNF-R55) appears to depend on protein intermediates that interact with specific cytoplasmic domains of TNF-R55. By combined use of the yeast interaction trap system and a peptide scanning library, the novel WD-repeat protein FAN has been identified, which specifically binds to a cytoplasmic nine amino acid binding motif of TNF-R55. This region has been previously recognized as a distinct functional domain that is both required and sufficient for the activation of neutral sphingomyelinase (N-SMase). Overexpression of full-length FAN enhanced N-SMase activity in TNF–treated cells, while truncated mutants of FAN produced dominant negative effects. The data suggest that FAN regulates ceramide production by N-SMase, which is a crucial step in TNF signaling

Bone Marrow-Derived Progenitor Cells Augment Venous Remodeling in a Mouse Dorsal Skinfold Chamber Model

The delivery of bone marrow-derived cells (BMDCs) has been widely used to stimulate angiogenesis and arteriogenesis. We identified a progenitor-enriched subpopulation of BMDCs that is able to augment venular remodeling, a generally unexplored area in microvascular research. Two populations of BMDCs, whole bone marrow (WBM) and Lin−/Sca-1+ progenitor cells, were encapsulated in sodium alginate and delivered to a mouse dorsal skinfold chamber model. Upon observation that encapsulated Sca-1+ progenitor cells enhance venular remodeling, the cells and tissue were analyzed on structural and molecular levels. Venule walls were thickened and contained more nuclei after Sca-1+ progenitor cell delivery. In addition, progenitors expressed mRNA transcript levels of chemokine (C-X-C motif) ligand 2 (CXCL2) and interferon gamma (IFNγ) that are over 5-fold higher compared to WBM. Tissues that received progenitors expressed significantly higher protein levels of vascular endothelial growth factor (VEGF), monocyte chemotactic protein-1 (MCP-1), and platelet derived growth factor-BB (PDGF-BB) compared to tissues that received an alginate control construct. Nine days following cell delivery, tissue from progenitor recipients contained 39% more CD45+ leukocytes, suggesting that these cells may enhance venular remodeling through the modulation of the local immune environment. Results show that different BMDC populations elicit different microvascular responses. In this model, Sca-1+ progenitor cell-derived CXCL2 and IFNγ may mediate venule enlargement via modulation of the local inflammatory environment