Researchers from 12 Sections, Laboratories, or Branches have used the Facility during the past year and 29 researchers have been newly trained to use one or several of the instruments. LIS staff have assisted Facility users to apply more demanding microscopy techniques, to improve the quality of their images, and to prepare these images for publication. NIAMS publications which have benefited from such help and/ or show images collected on our instruments are listed in the bibliography. LIS staff have also helped with evaluation of new instruments that Facility users are interested in. Microscopy done in LIS in the past year has contributed to expand knowledge in several NIAMS research target areas: i) understanding cartilage and its diseases (Gabay et al, 2012); ii) understanding skin development and diseases (Duverger et al., 2011 &2012;Okano et al., 2012) iii) understanding muscle development (Zaal et al., 2011) and muscle diseases (Feng et al., 2012). The pool of instruments has been considerably updated by the acquisition of the Zeiss 780 confocal microscope in replacement of the 10 year- old Zeiss 510. The new confocal is more sensitive and obtains better images while causing much less photodamage to tissues or cells. We have also increased the reach of the microscopy techniques available to NIAMS researchers by the addition of the Incucyte, a microscope that fits inside a tissue culture incubator for time-lapse imaging of cells in normal conditions. Other older instruments have been upgraded: a fast autofocusing system has been implemented on the TIRF microscope for perfect focal stability, and new lenses allow us now to take transmitted light or fluorescence images of cells grown on plastic dishes. Plastic dishes are often the best support for cells but they are traditionally the worst support from the viewpoint of microscopy because of their poor optical qualities. LIS Staff have played a lead role in the choice and implementation of a new online calendaring system for efficient reservations and monitoring of NIAMS instruments. The system went live in February 2012 and is now used by NIAMS staff to view information and reserve instruments in LIS as well as in the Flow Cytometry and Translational Immunology Sections and some of the Building 10 Laboratories/ Branches. Facility Staff have demonstrated the use of microscopy techniques to one group of visitors to NIH this year.

Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
2012
Total Cost
$2,359,952
Indirect Cost
Name
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Department
Type
DUNS #
City
State
Country
Zip Code
Iglesias-Bartolome, Ramiro; Uchiyama, Akihiko; Molinolo, Alfredo A et al. (2018) Transcriptional signature primes human oral mucosa for rapid wound healing. Sci Transl Med 10:
Sarshad, Aishe A; Juan, Aster H; Muler, Ana Iris Correa et al. (2018) Argonaute-miRNA Complexes Silence Target mRNAs in the Nucleus of Mammalian Stem Cells. Mol Cell :
Duverger, Olivier; Carlson, Jenna C; Karacz, Chelsea M et al. (2018) Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay. PLoS Genet 14:e1007168
Feng, Li Rebekah; Fernández-Martínez, Juan Luis; Zaal, Kristien J M et al. (2018) mGluR5 mediates post-radiotherapy fatigue development in cancer patients. Transl Psychiatry 8:110
Lee, Jeansun; Dieckmann, Nele M G; Edgar, James R et al. (2018) Fas Ligand localizes to intraluminal vesicles within NK cell cytolytic granules and is enriched at the immune synapse. Immun Inflamm Dis 6:312-321
Wolf, M; Ao, M; Chavez, M B et al. (2018) Reduced Orthodontic Tooth Movement in Enpp1 Mutant Mice with Hypercementosis. J Dent Res 97:937-945
Gupta, Sarthak; Chan, Diana W; Zaal, Kristien J et al. (2018) A High-Throughput Real-Time Imaging Technique To Quantify NETosis and Distinguish Mechanisms of Cell Death in Human Neutrophils. J Immunol 200:869-879
Thumbigere Math, V; Rebouças, P; Giovani, P A et al. (2018) Periodontitis in Chédiak-Higashi Syndrome: An Altered Immunoinflammatory Response. JDR Clin Trans Res 3:35-46
Bhattacharya, Shreya; Kim, Jin-Chul; Ogawa, Youichi et al. (2018) DLX3-Dependent STAT3 Signaling in Keratinocytes Regulates Skin Immune Homeostasis. J Invest Dermatol 138:1052-1061
Sikora, Keith A; Bennett, Joshua R; Vyncke, Laurens et al. (2018) Germline gain-of-function myeloid differentiation primary response gene-88 (MYD88) mutation in a child with severe arthritis. J Allergy Clin Immunol 141:1943-1947.e9

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