Chondrogenic differentiation of stem cells in human umbilical cord stroma with PGA and PLLA scaffolds

The stem cells in the umbilical cord stroma, or Wharton's jelly, are referred to as human umbilical cord mesenchymal stromal cells (hUCMSCs) and have been shown to differentiate along a chondrogenic lineage. The aim of this study was to evaluate the chondrogenic differentiation of hUCMSCs in either polyglycolic acid (PGA) or poly-L-lactic acid (PLLA) non-woven mesh scaffolds for cartilage tissue engineering. PGA is widely known to degrade faster than PLLA, and over longer time scales, and differences may be expected to emerge after extended culture periods. Therefore, the focus of this study was to evaluate differences over a shorter duration. After 21 days of culture in PLLA or PGA scaffolds, hUCMSC constructs were analyzed for biochemical content, histology, and gene expression. Overall, there were only minute differences between the two scaffold groups, with similar gene expression and biosynthesis. The most notable difference was a change in shape from cylindrical to spherical by the PGA, but not PLLA, scaffold group. The overall similar behavior of the groups may suggest that in vivo application of hUCMSC-seeded PLLA or PGA scaffolds, following a 21-day pre-culture period, may yield similar constructs at the time of implantation. However, differences may begin to become more apparent with in vivo performance following implantation, or with in vitro performance over longer time periods.We gratefully acknowledge Dr. Xinkun Wang for his guidance in performing the RT-PCR. We also thank Dr. Limin Wang for his RT-PCR assistance, and Lauren Byers for her assistance in proofreading the manuscript. This study was supported by NIH R21 grant DE017673-01, Arthritis Foundation (National and Kansas Chapters), and the State of Kansas

Enhanced ethanol production from stalk juice of sweet sorghum by response surface methodology

Sweet sorghum (sugar sorghum, Sorghum bicolor) is one kind of non-grain energy crops. As a novel green regenerated high-energy crop with high utility value, high yield of biomass, the sweet sorghum is widely used and developed in China. Stalk juice of sweet sorghum was used as the main substrate for ethanol production by a Saccharomyces cerevisiae strain because of the high content of sugar. Effects of different medium compositions, including urea, KH2PO4 and MgSO4, on ethanol production were studied by response surface methodology in this paper. A second-order model that related the concentration of ethanol was developed and thus the optimal medium composition was obtained, which was 4.75 g l-1 urea, 3.58 g l-1 KH2PO4, and 0.98 g l-1 MgSO4. Under this condition, the highest ethanol concentration reached 86.2 g l-1.Key words: Ethanol, sweet sorghum, stalk juice, medium composition, response surface methodology

Human umbilical cord mesenchymal stromal cells in a sandwich approach for osteochondral tissue engineering

Cell sources and tissue integration between cartilage and bone regions are critical to successful osteochondral regeneration. In this study, human umbilical cord mesenchymal stromal cells (hUCMSCs), derived from Wharton's jelly, were introduced to the field of osteochondral tissue engineering and a new strategy for osteochondral integration was developed by sandwiching a layer of cells between chondrogenic and osteogenic constructs before suturing them together. Specifically, hUCMSCs were cultured in biodegradable poly‐ L ‐lactic acid scaffolds for 3 weeks in either chondrogenic or osteogenic medium to differentiate cells toward cartilage or bone lineages, respectively. A highly concentrated cell solution containing undifferentiated hUCMSCs was pasted onto the surface of the bone layer at week 3 and the two layers were then sutured together to form an osteochondral composite for another 3 week culture period. Chondrogenic and osteogenic differentiation was initiated during the first 3 weeks, as evidenced by the expression of type II collagen and runt‐related transcription factor 2 genes, respectively, and continued with the increase of extracellular matrix during the last 3 weeks. Histological and immunohistochemical staining, such as for glycosaminoglycans, type I collagen and calcium, revealed better integration and transition of these matrices between two layers in the composite group containing sandwiched cells compared to other control composites. These results suggest that hUCMSCs may be a suitable cell source for osteochondral regeneration, and the strategy of sandwiching cells between two layers may facilitate scaffold and tissue integration. Copyright © 2010 John Wiley & Sons, Ltd.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/87014/1/370_ftp.pd

Human umbilical cord mesenchymal stromal cells in a sandwich approach for osteochondral tissue engineering

This is the peer reviewed version of the following article: Wang, L., Zhao, L., & Detamore, M. S. (2011). Human umbilical cord mesenchymal stromal cells in a sandwich approach for osteochondral tissue engineering. Journal of Tissue Engineering and Regenerative Medicine, 5(9), 712–721. http://doi.org/10.1002/term.370, which has been published in final form at http://doi.org/10.1002/term.370. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.Cell sources and tissue integration between cartilage and bone regions are critical to successful osteochondral regeneration. In this study, human umbilical cord mesenchymal stromal cells (hUCMSCs), derived from Wharton’s jelly, were introduced to the field of osteochondral tissue engineering and a new strategy for osteochondral integration was developed by sandwiching a layer of cells between chondrogenic and osteogenic constructs before suturing them together. Specifically, hUCMSCs were cultured in biodegradable poly-l-lactic acid scaffolds for 3 weeks in either chondrogenic or osteogenic medium to differentiate cells toward cartilage or bone lineages, respectively. A highly concentrated cell solution containing undifferentiated hUCMSCs was pasted onto the surface of the bone layer at week 3 and the two layers were then sutured together to form an osteochondral composite for another 3 week culture period. Chondrogenic and osteogenic differentiation was initiated during the first 3 weeks, as evidenced by the expression of type II collagen and runt-related transcription factor 2 genes, respectively, and continued with the increase of extracellular matrix during the last 3 weeks. Histological and immunohistochemical staining, such as for glycosaminoglycans, type I collagen and calcium, revealed better integration and transition of these matrices between two layers in the composite group containing sandwiched cells compared to other control composites. These results suggest that hUCMSCs may be a suitable cell source for osteochondral regeneration, and the strategy of sandwiching cells between two layers may facilitate scaffold and tissue integration

Covariant density functional theory for antimagnetic rotation

Following the previous letter on the first microscopic description of the antimagnetic rotation (AMR) in 105Cd, a systematic investigation and detailed analysis for the AMR band in the frame-work of tilted axis cranking (TAC) model based on covariant density functional theory are carried out. After performing the microscopic and self-consistentTAC calculations with an given density functional, the configuration for the observed AMR band in 105Cd is obtained from the single-particle Routhians. With the configuration thus obtained, the tilt angle for a given rotational frequency is determined self-consistently by minimizing the total Routhian with respect to the tilt angle. In such a way, the energy spectrum, total angular momenta, kinetic and dynamic moments of inertia, and the B(E2) values for the AMR band in 105Cd are calculated. Good agreement with the data is found. By investigating microscopically the contributions from neutrons and protons to the total angular momentum, the "two-shears-like" mechanism in the AMR band is clearly illus-trated. Finally, the currents leading to time-odd mean fields in the Dirac equation are presented and discussed in detail. It is found that they are essentially determined by the valence particles and/or holes. Their spatial distribution and size depend onthe specific single-particle orbitals and the rotational frequency.Comment: 35 pages, 17 figures, accepted by Phys. Rev.

Region-specific and activity-dependent regulation of SVZ neurogenesis and recovery after stroke.

Stroke is the leading cause of adult disability. Neurogenesis after stroke is associated with repair; however, the mechanisms regulating poststroke neurogenesis and its functional effect remain unclear. Here, we investigate multiple mechanistic routes of induced neurogenesis in the poststroke brain, using both a forelimb overuse manipulation that models a clinical neurorehabilitation paradigm, as well as local manipulation of cellular activity in the peri-infarct cortex. Increased activity in the forelimb peri-infarct cortex via either modulation drives increased subventricular zone (SVZ) progenitor proliferation, migration, and neuronal maturation in peri-infarct cortex. This effect is sensitive to competition from neighboring brain regions. By using orthogonal tract tracing and rabies virus approaches in transgenic SVZ-lineage-tracing mice, SVZ-derived neurons synaptically integrate into the peri-infarct cortex; these effects are enhanced with forelimb overuse. Synaptic transmission from these newborn SVZ-derived neurons is critical for spontaneous recovery after stroke, as tetanus neurotoxin silencing specifically of the SVZ-derived neurons disrupts the formation of these synaptic connections and hinders functional recovery after stroke. SVZ-derived neurogenesis after stroke is activity-dependent, region-specific, and sensitive to modulation, and the synaptic connections formed by these newborn cells are functionally critical for poststroke recovery

Performance Analysis for Control- and User-Plane Separation based RAN with Non-Uniformly Distributed Users

In the control- and user-plane separation (CUPS) based radio access networks (RANs), control-signaling and data are transmitted by the control base stations (CBSs) and data base stations (DBSs), respectively. However, existing studies usually model the C/U-planes as two separate homogeneous networks, neglecting the dependence among the two planes and users. To address this problem, we analyze the coverage probability, spectrum efficiency (SE) and delay considering the dependent features among CBSs, DBSs, and non-uniformly distributed users based on stochastic geometry. Firstly, we present an analytical model for CUPS, where the DBSs are deployed at user hotspots based on Poisson point processes (PPPs), users are clustered around DBSs based on Poisson cluster processes (PCPs), and CBSs are deployed according to a dependent thinning of locations of DBSs based on Matérn hard-core processes (MHCPs). Secondly, we design novel distance-based fractional frequency reuse (FFR) schemes by exploiting the properties of PCP and MHCP to improve the coverage of cell edge users. Thirdly, we derive the distributions of user downlink rates, which are used to analyze the average queueing delay under M/M/C queueing model. Numerical results are presented to verify the efficiency of the proposed model compared to independently distributed BSs and users, and show the dependent BS deployment could significantly improve the coverage of the network

A C-Terminal Heat Shock Protein 90 Inhibitor Decreases Hyperglycemia-induced Oxidative Stress and Improves Mitochondrial Bioenergetics in Sensory Neurons

Diabetic peripheral neuropathy (DPN) is a common complication of diabetes in which hyperglycemia-induced mitochondrial dysfunction and enhanced oxidative stress contribute to sensory neuron pathology. KU-32 is a novobiocin-based, C-terminal inhibitor of the molecular chaperone, heat shock protein 90 (Hsp90). KU-32 ameliorates multiple sensory deficits associated with the progression of DPN and protects unmyelinated sensory neurons from glucose-induced toxicity. Mechanistically, KU-32 increased the expression of Hsp70 and this protein was critical for drug efficacy in reversing DPN. However, it remained unclear if KU-32 had a broader effect on chaperone induction and if its efficacy was linked to improving mitochondrial dysfunction. Using cultures of hyperglycemically stressed primary sensory neurons, the present study investigated whether KU-32 had an effect on the translational induction of other chaperones and improved mitochondrial oxidative stress and bioenergetics. A variation of stable isotope labeling with amino acids in cell culture called pulse SILAC (pSILAC) was used to unbiasedly assess changes in protein translation. Hyperglycemia decreased the translation of numerous mitochondrial proteins that affect superoxide levels and respiratory activity. Importantly, this correlated with a decrease in mitochondrial oxygen consumption and an increase in superoxide levels. KU-32 increased the translation of Mn superoxide dismutase and several cytosolic and mitochondrial chaperones. Consistent with these changes, KU-32 decreased mitochondrial superoxide levels and significantly enhanced respiratory activity. These data indicate that efficacy of modulating molecular chaperones in DPN may be due in part to improved neuronal mitochondrial bioenergetics and decreased oxidative stress