The Silent Struggle: A Journey to Find My Voice

Dartmouth can be a great place, full of opportunities to push ourselves to learn and grow in ways we didn’t know we could. But it took me two and a half years to realize how truly special this place is and how I fit into it. It took me leaving the physical confines of Dartmouth to realize that I can control my life, my choices, my happiness. It took me studying thousands of miles from this place to realize that I have a place right here, at Dartmouth

Sclerochronological studies in the humboldt current system, a highly variable ecosystem

The Humboldt Current that bathes the west coast of South America is affected by different influences at daily to decadal periodicities. Environmental influences such as upwelling or coastal trapped waves as well as climate influences such as El Nino southern oscillation and Pacific decadal oscillation events interact and modify the thermonutricline depth of this Humboldt Current System. The position of this thermonutricline plays a key role in Humboldt Current System functioning by driving sea surface temperature (SST) and primary production variations. As filter feeders, bivalves are particularly affected by SST and primary production, and their shells can provide information about these two environmental factors. Using sclerochronology, we studied three bivalve species from different ecological niches living along the Peruvian-Chilean coast. Depending on the species, thick or thin sections, etched or not, were studied using an optical microscope. Increment thicknesses were measured at the surface of the shell and/or in cross-section. Moreover, the mineralogical composition of the different layers of the studied shells was determined on thin sections by Fourier transform infrared spectroscopic analyses. Growth results were then interpreted tentatively in terms of environmental variations. For the free-living, short-lived Pectinidae Argopecten purpuratus, the daily growth rhythm is linked to the solar period whereas growth amplitude seems to be related to the occurrence of spawning events, probably triggered by specific water temperature patterns. tidal regime and SST seem to be the major environmental parameters that govern shell growth rhythms and/or increment thickness for two nearshore species-the Mytilidae Choromytilus chorus and the Veneridae Eurhomalea rufa-which grow more slowly and have a life span longer than A. purpuratus, and have a strong potential for paleo-environmental and paleo-El Nino southern oscillation reconstruction. These results need to be confirmed studying multiple shells to quantify individual growth variations and to enhance the significance of the findings on the different environmental parameters recorded in the growth patterns of the South American bivalve species studied

Chromosomal Localization of the Carcinoembryonic Antigen Gene Family and Differential Expression in Various Tumors

Carcinoembryonic antigen (CEA) is a glycoprotein which is important as a tumor marker for a number of human cancers. It is a member of a gene family comprising about 10 closely related genes. In order to characterize mUNAs transcribed from individual genes we have identified by DNA and RNA hybridization experiments, gene-specific sequences from the 3 ' noncoding regions of CEA, and of nonspecific cross-reacting antigen (NCA) mRNAs, which have been recently cloned. With these probes, CEA mRNAs with lengths of 3.5 and 3.0 kilobases and an NCA mRNA species of 2.5 kilobases were identified in various human tumors. A 2.2-kilobase mRNA species, however, could only be detected in leu kocytes of patients with chronic myeloid leukemia by hybridization with a probe from the immunoglobulin-like repeat domain of CEA. This region is known to be very similar among the various members of the CEA gene family, and indeed the probe hybridizes with all four mRNA species. In situ hybridization with a cross-hybridizing probe from the NCA gene localized the members of the CEA gene family to the short and to the long arm of chromosome 19. In addition, a CEA cDNA probe was found to hybridize to the long arm of chromosome 19 only

The Calcitonin Receptor Gene Is a Candidate for Regulation of Susceptibility to Herpes simplex Type 1 Neuronal Infection Leading to Encephalitis in Rat

Herpes simplex encephalitis (HSE) is a fatal infection of the central nervous system (CNS) predominantly caused by Herpes simplex virus type 1. Factors regulating the susceptibility to HSE are still largely unknown. To identify host gene(s) regulating HSE susceptibility we performed a genome-wide linkage scan in an intercross between the susceptible DA and the resistant PVG rat. We found one major quantitative trait locus (QTL), Hse1, on rat chromosome 4 (confidence interval 24.3–31 Mb; LOD score 29.5) governing disease susceptibility. Fine mapping of Hse1 using recombinants, haplotype mapping and sequencing, as well as expression analysis of all genes in the interval identified the calcitonin receptor gene (Calcr) as the main candidate, which also is supported by functional studies. Thus, using unbiased genetic approach variability in Calcr was identified as potentially critical for infection and viral spread to the CNS and subsequent HSE development

Disease-specific oligodendrocyte lineage cells arise in multiple sclerosis

Multiple sclerosis (MS) is characterized by an immune system attack targeting myelin, which is produced by oligodendrocytes (OLs). We performed single-cell transcriptomic analysis of OL lineage cells from the spinal cord of mice induced with experimental autoimmune encephalomyelitis (EAE), which mimics several aspects of MS. We found unique OLs and OL precursor cells (OPCs) in EAE and uncovered several genes specifically alternatively spliced in these cells. Surprisingly, EAE-specific OL lineage populations expressed genes involved in antigen processing and presentation via major histocompatibility complex class I and II (MHC-I and -II), and in immunoprotection, suggesting alternative functions of these cells in a disease context. Importantly, we found that disease-specific oligodendroglia are also present in human MS brains and that a substantial number of genes known to be susceptibility genes for MS, so far mainly associated with immune cells, are expressed in the OL lineage cells. Finally, we demonstrate that OPCs can phagocytose and that MHC-II-expressing OPCs can activate memory and effector CD4-positive T cells. Our results suggest that OLs and OPCs are not passive targets but instead active immunomodulators in MS. The disease-specific OL lineage cells, for which we identify several biomarkers, may represent novel direct targets for immunomodulatory therapeutic approaches in MS