The histotechnology core will function to provide extensive services to each of the four projects. The services can be grouped in three specific areas, which are utilized in the analysis of in vivo models of angiogenesis. First, services are provided in the procurement of tissue, including specialized fixation and perfusion fixation needed for vessel morphometric analysis. In the second aspect, harvested tissues are processed for routine histology, and a wide range of immunohistochemical techniques. Lastly, service is provide in the imaging of such histology and immunohistochemistry, by the use of electron microscopy and confocal imaging. These imaging techniques also include statistical morphometric analysis and digital image analysis. Thus, the core facility will provide a complete range of services for projects utilizing in vivo models, with oversight by a single PI and technical support staff to standardize procedures and maintain quality control, and to facilitate interactions with the extensive imaging facilities at Weill Medical College. Additionally, this will result in significant savings in terms of immunohistochemical supplies, and in tissue preparation and sectioning, as well as reduced rates for the imaging facility.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
1P01HL067839-01
Application #
6531594
Study Section
Special Emphasis Panel (ZHL1)
Project Start
2001-09-27
Project End
2006-06-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Morozova, Kateryna; Sridhar, Sunandini; Sidhar, Sunandini et al. (2015) Annexin A2 promotes phagophore assembly by enhancing Atg16L? vesicle biogenesis and homotypic fusion. Nat Commun 6:5856
Klenotic, Philip A; Page, Richard C; Li, Wei et al. (2013) Molecular basis of antiangiogenic thrombospondin-1 type 1 repeat domain interactions with CD36. Arterioscler Thromb Vasc Biol 33:1655-62
Klenotic, Philip A; Page, Richard C; Misra, Saurav et al. (2011) Expression, purification and structural characterization of functionally replete thrombospondin-1 type 1 repeats in a bacterial expression system. Protein Expr Purif 80:253-9
Ding, Bi-Sen; Nolan, Daniel J; Butler, Jason M et al. (2010) Inductive angiocrine signals from sinusoidal endothelium are required for liver regeneration. Nature 468:310-5
Rabbany, Sina Y; James, Daylon; Rafii, Shahin (2010) New dimensions in vascular engineering: opportunities for cancer biology. Tissue Eng Part A 16:2157-9
Yamamoto, Masaya; James, Daylon; Li, Hui et al. (2010) Generation of stable co-cultures of vascular cells in a honeycomb alginate scaffold. Tissue Eng Part A 16:299-308
Butler, Jason M; Kobayashi, Hideki; Rafii, Shahin (2010) Instructive role of the vascular niche in promoting tumour growth and tissue repair by angiocrine factors. Nat Rev Cancer 10:138-46
Butler, Jason M; Nolan, Daniel J; Vertes, Eva L et al. (2010) Endothelial cells are essential for the self-renewal and repopulation of Notch-dependent hematopoietic stem cells. Cell Stem Cell 6:251-64
Klenotic, Philip A; Huang, Ping; Palomo, Juan et al. (2010) Histidine-rich glycoprotein modulates the anti-angiogenic effects of vasculostatin. Am J Pathol 176:2039-50
James, Daylon; Nam, Hyung-song; Seandel, Marco et al. (2010) Expansion and maintenance of human embryonic stem cell-derived endothelial cells by TGFbeta inhibition is Id1 dependent. Nat Biotechnol 28:161-6

Showing the most recent 10 out of 54 publications