Entry of Human Papillomavirus Type 16 by Actin-Dependent, Clathrin- and Lipid Raft-Independent Endocytosis

Infectious endocytosis of incoming human papillomavirus type 16 (HPV-16), the main etiological agent of cervical cancer, is poorly characterized in terms of cellular requirements and pathways. Conflicting reports attribute HPV-16 entry to clathrin-dependent and -independent mechanisms. To comprehensively describe the cell biological features of HPV-16 entry into human epithelial cells, we compared HPV-16 pseudovirion (PsV) infection in the context of cell perturbations (drug inhibition, siRNA silencing, overexpression of dominant mutants) to five other viruses (influenza A virus, Semliki Forest virus, simian virus 40, vesicular stomatitis virus, and vaccinia virus) with defined endocytic requirements. Our analysis included infection data, i.e. GFP expression after plasmid delivery by HPV-16 PsV, and endocytosis assays in combination with electron, immunofluorescence, and video microscopy. The results indicated that HPV-16 entry into HeLa and HaCaT cells was clathrin-, caveolin-, cholesterol- and dynamin-independent. The virus made use of a potentially novel ligand-induced endocytic pathway related to macropinocytosis. This pathway was distinct from classical macropinocytosis in regards to vesicle size, cholesterol-sensitivity, and GTPase requirements, but similar in respect to the need for tyrosine kinase signaling, actin dynamics, Na+/H+ exchangers, PAK-1 and PKC. After internalization the virus was transported to late endosomes and/or endolysosomes, and activated through exposure to low pH

Absorption-based assays for the analysis of osteogenic and chondrogenic yield

The typical characteristics of cartilage and bone tissue are their unique extracellular matrices on which our body relies for structural support. In the respective tissue, the cells that create these matrices are the chondrocyte and the osteoblast. During in vitro differentiation from an embryonic or any other stem cell, specific cell types must be unequivocally identifiable to be able to draw the conclusion that a specific cell type has indeed been generated. Here, gene expression profiling can be helpful, but examining functional properties of cells is a lot more conclusive. As proteoglycans are found in and are part of the function of cartilage tissue, their detection and quantification becomes an important diagnostic tool in tissue engineering. Likewise, in bone regeneration therapy and in research, alkaline phosphatase is a known marker to detect the degree of development and function of differentiating osteoblasts. Calcification of the maturing osteoblast is the last stage in its development, and thus, the quantification of deposited calcium can aid in determining how many cells in a given culture have successfully matured into fully functioning osteoblasts. This chapter describes methods ideal for testing of proteoglycan content, alkaline phosphatase activity, and calcium deposit during in vitro chondro- and osteogenesis

Nanoscale Effects in Water Splitting Photocatalysis.

From a conceptual standpoint, the water photoelectrolysis reaction is the simplest way to convert solar energy into fuel. It is widely believed that nanostructured photocatalysts can improve the efficiency of the process and lower the costs. Indeed, nanostructured light absorbers have several advantages over traditional materials. This includes shorter charge transport pathways and larger redox active surface areas. It is also possible to adjust the energetics of small particles via the quantum size effect or with adsorbed ions. At the same time, nanostructured absorbers have significant disadvantages over conventional ones. The larger surface area promotes defect recombination and reduces the photovoltage that can be drawn from the absorber. The smaller size of the particles also makes electron-hole separation more difficult to achieve. This chapter discusses these issues using selected examples from the literature and from the laboratory of the author