Engineered functional organs or tissues, created with autologous somatic cells and seeded on biodegradable or hydrogel scaffolds, have been developed for use in individuals with tissue damage suffered from congenital disorders, infection, irradiation, or cancer. However, in those patients, abnormal cells obtained by biopsy from the compromised tissue could potentially contaminate the engineered tissues. Thus, an alternative cell source for construction of the neo-organ or functional recovery of the injured or diseased tissues would be useful. Recently, we have found stem cells existing in the urine. These cells are highly expandable, and have self-renewal capacity, paracrine properties, and multi-differentiation potential. As a novel cell source, urine-derived stem cells (USCs) provide advantages for cell therapy and tissue engineering applications in regeneration of various tissues, particularly in the genitourinary tract, because they originate from the urinary tract system. Importantly, USCs can be obtained via a non-invasive, simple, and low-cost approach and induced with high efficiency to differentiate into three dermal cell lineages.

Fluidic adaptive lenses with an adjustable focal length over a wide range were demonstrated in this letter. The focal length adjustment was achieved by changing the shape of the fluidic lens without any mechanical moving parts. The shortest focal length demonstrated in such devices is 41 mm, which corresponds to a large numerical aperture of 0.24 and a small F number of 2.05. The highest resolution measured using a positive standard is 25.39 lp/mm in this fluidic adaptive lens.

Fluorescent colloidal particles, fabricated by depositing a thin gold film on one side of the particle, show intensity fluctuation (blinking) under an optical microscope because of their rotational Brownian motion. Interactions between molecules immobilized on the surfaces of the particle and the solid substrate restrict the rotation of the particle, thus modulating the intensity fluctuations. Because we can obtain the time-dependent rotational angle from the fluorescent intensity, we can use the intensity signals to investigate the weak interactions between unlabeled molecules by analyzing the angular distribution of the particle. To the best of our knowledge, this is the first demonstration of an optical measurement of the rotations of nanoparticles and the first attempt at using such a technique to study molecular interactions.