designing-microfluidic-devices-for-studying-cellular-responses-under

Designing Microfluidic Devices for Studying Cellular Responses Under Single or Coexisting Chemical/Electrical/Shear Stress Stimuli

Microfluidic devices are capable of creating a precise and controllable cellular micro-environment of pH, temperature, salt concentration, and other ...

National Taiwan University

Previous phylogenetic studies based on DNA sequence data have partially resolved taxonomic relationships among Pestalotiopsis species. There are still some morphological characters whose phylogenetic significance have not been assessed properly due to limited taxon sampling, in particular the degree of pigmentation of median cells. In this study, the stability of pigmentation of median cells of conidia in Pestalotiopsis species was evaluated in subculture, and a molecular phylogenetic analysis was conducted on 45 strains belonging to 26 species in order to reappraise the pigmentation of median cells for its significance in the taxonomy of Pestalotiopsis. Phylogenetic relationships were inferred from nucleotide sequences in ITS regions (ITS1, 5.8S and ITS2) and β-tubulin 2 gene (tub2). The results showed that pigmentation of median cells was stable and it could be a key character in the taxonomy of Pestalotiopsis species. Instead of "concolorous" and "versicolor" proposed by Steyeart (1949), "brown to olivaceous" and "umber to fuliginous" are described and proposed in this paper.

Cultural studies coupled with DNA based sequence analyses and its implication on pigmentation as a phylogenetic marker in Pestalotiopsis taxonomy.

We report experimental as well as theoretical investigation of the key factors that influence the relative timing jitter between hybrid synchronized ultrafast Yb and Er fiber laser systems. Experimental results show that, within the achievable synchronization range, the synchronization performance varies significantly with the relative injection timing between the 1 μm master and 1.5 μm slave pulses. This observation is in agreement with the insights obtained from the theoretical analysis, which identifies the retiming effect as a function of the initial condition of the master-slave pulse collision. By controlling the relative injection timing with a low-bandwidth intracavity feedback, relative timing jitter as low as 0.87 fs (within 1.9 MHz bandwidth) is successfully obtained.

Subfemtosecond hybrid synchronization between ultrafast Yb and Er fiber laser systems by controlling the relative injection timing.

Stabilization of the relative carrier-envelope (CE) phase for hybridly synchronized two-color fs Yb and Er fiber-laser systems is demonstrated for the first time by utilizing the feed-forward scheme based on an acousto-optic frequency shifter. The slow drift issues arising from the feed-forward scheme are solved by adding the in-loop relative CE frequency coarse stabilization via modulating the laser pump current. Sub-fs timing locking between the two-color pulses is still maintained due to the fast response and large locking range of hybrid synchronization. The approach provides an alternative way to obtain phase-stable synchronized two-color pulses with higher pulse energies.

Relative carrier-envelope phase stabilization of hybridly synchronized ultrafast Yb and Er fiber-laser systems with the feed-forward scheme.

Reactive oxygen species (ROS) act as second messengers for redox modification of transcription factors essential for differentiation. The nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, a major source of ROS, has been shown to regulate differentiation of various progenitor cells, while its role in pancreatic endocrine cell differentiation is unclear. This study was aimed at this knowledge gap.

NADPH Oxidase-Dependent Reactive Oxygen Species Stimulate β-Cell Regeneration Through Differentiation of Endocrine Progenitors in Murine Pancreas.

Cell migration is an essential process involved in the development and maintenance of multicellular organisms. Electric fields (EFs) are one of the many physical and chemical factors known to affect cell migration, a phenomenon termed electrotaxis or galvanotaxis. In this paper, a microfluidics chip was developed to study the migration of cells under different electrical and chemical stimuli. This chip is capable of providing four different strengths of EFs in combination with two different chemicals via one simple set of agar salt bridges and Ag/AgCl electrodes. NIH 3T3 fibroblasts were seeded inside this chip to study their migration and reactive oxygen species (ROS) production in response to different EF strengths and the presence of β-lapachone. We found that both the EF and β-lapachone level increased the cell migration rate and the production of ROS in an EF-strength-dependent manner. A strong linear correlation between the cell migration rate and the amount of intracellular ROS suggests that ROS are an intermediate product by which EF and β-lapachone enhance cell migration. Moreover, an anti-oxidant, α-tocopherol, was found to quench the production of ROS, resulting in a decrease in the migration rate.

Correlation between cell migration and reactive oxygen species under electric field stimulation.

Collective cell migration plays important roles in many physiological processes such as embryonic development, tissue repair, and angiogenesis. A "wound" occurs when epithelial cells are lost and/or damaged due to some external factors, and collective cell migration takes place in the following wound-healing process. To study this cellular behavior, various kinds of wound-healing assays are developed. In these assays, a "wound," or a "cell-free region," is created in a cell monolayer mechanically, chemically, optically, or electrically. These assays are useful tools in studying the effects of certain physical or chemical stimuli on the wound-healing process. Most of these methods have disadvantages such as creating wounds of different sizes or shapes, yielding batch-to-batch variation, and damaging the coating of the cell culture surface. In this study, we used ultraviolet (UV) lights to selectively kill cells and create a wound out of a cell monolayer. A comparison between the current assay and the traditional scratch assay was made, indicating that these two methods resulted in similar wound-healing rates. The advantages of this UV-created wound-healing assay include fast and easy procedure, high throughput, and no direct contact to cells.

Article	Year
Cultural studies coupled with DNA based sequence analyses and its implication on pigmentation as a phylogenetic marker in Pestalotiopsis taxonomy. Molecular phylogenetics and evolution\| PubMed ID: 20692352	2010
Subfemtosecond hybrid synchronization between ultrafast Yb and Er fiber laser systems by controlling the relative injection timing. Optics letters\| PubMed ID: 23988983	2013
Relative carrier-envelope phase stabilization of hybridly synchronized ultrafast Yb and Er fiber-laser systems with the feed-forward scheme. Optics letters\| PubMed ID: 25768158	2015
NADPH Oxidase-Dependent Reactive Oxygen Species Stimulate β-Cell Regeneration Through Differentiation of Endocrine Progenitors in Murine Pancreas. Antioxidants & redox signaling\| PubMed ID: 26464216	2016
Correlation between cell migration and reactive oxygen species under electric field stimulation. Biomicrofluidics\| PubMed ID: 26487906	2015
A Wound-Healing Assay Based on Ultraviolet Light Ablation. Journal of laboratory automation\| PubMed ID: 27139694	2016

Shang-Ying Wu

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