The deuteron: structure and form factors

A brief review of the history of the discovery of the deuteron in provided. The current status of both experiment and theory for the elastic electron scattering is then presented.Comment: 80 pages, 33 figures, submited to Advances in Nuclear Physic

Positional Cloning of a Type 2 Diabetes Quantitative Trait Locus; Tomosyn-2, a Negative Regulator of Insulin Secretion

We previously mapped a type 2 diabetes (T2D) locus on chromosome 16 (Chr 16) in an F2 intercross from the BTBR T (+) tf (BTBR) Lepob/ob and C57BL/6 (B6) Lepob/ob mouse strains. Introgression of BTBR Chr 16 into B6 mice resulted in a consomic mouse with reduced fasting plasma insulin and elevated glucose levels. We derived a panel of sub-congenic mice and narrowed the diabetes susceptibility locus to a 1.6 Mb region. Introgression of this 1.6 Mb fragment of the BTBR Chr 16 into lean B6 mice (B6.16BT36–38) replicated the phenotypes of the consomic mice. Pancreatic islets from the B6.16BT36–38 mice were defective in the second phase of the insulin secretion, suggesting that the 1.6 Mb region encodes a regulator of insulin secretion. Within this region, syntaxin-binding protein 5-like (Stxbp5l) or tomosyn-2 was the only gene with an expression difference and a non-synonymous coding single nucleotide polymorphism (SNP) between the B6 and BTBR alleles. Overexpression of the b-tomosyn-2 isoform in the pancreatic β-cell line, INS1 (832/13), resulted in an inhibition of insulin secretion in response to 3 mM 8-bromo cAMP at 7 mM glucose. In vitro binding experiments showed that tomosyn-2 binds recombinant syntaxin-1A and syntaxin-4, key proteins that are involved in insulin secretion via formation of the SNARE complex. The B6 form of tomosyn-2 is more susceptible to proteasomal degradation than the BTBR form, establishing a functional role for the coding SNP in tomosyn-2. We conclude that tomosyn-2 is the major gene responsible for the T2D Chr 16 quantitative trait locus (QTL) we mapped in our mouse cross. Our findings suggest that tomosyn-2 is a key negative regulator of insulin secretion

Scaffold-free human mesenchymal stem cell construct geometry regulates long bone regeneration

Biomimetic bone tissue engineering strategies partially recapitulate development. We recently showed functional restoration of femoral defects using scaffold-free human mesenchymal stem cell (hMSC) condensates featuring localized morphogen presentation with delayed in vivo mechanical loading. Possible effects of construct geometry on healing outcome remain unclear. Here, we hypothesized that localized presentation of transforming growth factor (TGF)-β1 and bone morphogenetic protein (BMP)-2 to engineered hMSC tubes mimicking femoral diaphyses induces endochondral ossification, and that TGF-β1 + BMP-2-presenting hMSC tubes enhance defect healing with delayed in vivo loading vs. loosely packed hMSC sheets. Localized morphogen presentation stimulated chondrogenic priming/endochondral differentiation in vitro. Subcutaneously, hMSC tubes formed cartilage templates that underwent bony remodeling. Orthotopically, hMSC tubes stimulated more robust endochondral defect healing vs. hMSC sheets. Tissue resembling normal growth plate was observed with negligible ectopic bone. This study demonstrates interactions between hMSC condensation geometry, morphogen bioavailability, and mechanical cues to recapitulate development for biomimetic bone tissue engineering

Changing geographies of immigration and religion in the U.S. south

cited By 1This chapter examines the internal workings of faith communities in the U.S. South and how they are deeply enmeshed in every-day productions and negotiations of societal membership, citizenship rights, and immigrant integration. We begin with a brief overview of recent immigration and the ways it has complicated the region?s social and political landscape in the region. We then discuss the diversity of immigrant faith communities and the very different ways that established faith communities have tried to incorporate immigrants. Drawing on our research on faith communities in Charlotte, NC, Greenville-Spartanburg, SC, and Atlanta, GA we show how faith communities, both Christian and non-Christian, are producing diverse conceptions of social difference and societal membership. Our aim is to convey how ideas about citizenship are molded in faith-community contexts and the ways that these processes are shaped by particular regional histories

Changing geographies of immigration and religion in the U.S. south

cited By 1This chapter examines the internal workings of faith communities in the U.S. South and how they are deeply enmeshed in every-day productions and negotiations of societal membership, citizenship rights, and immigrant integration. We begin with a brief overview of recent immigration and the ways it has complicated the region?s social and political landscape in the region. We then discuss the diversity of immigrant faith communities and the very different ways that established faith communities have tried to incorporate immigrants. Drawing on our research on faith communities in Charlotte, NC, Greenville-Spartanburg, SC, and Atlanta, GA we show how faith communities, both Christian and non-Christian, are producing diverse conceptions of social difference and societal membership. Our aim is to convey how ideas about citizenship are molded in faith-community contexts and the ways that these processes are shaped by particular regional histories