Our biomedical goal is to better characterize the function of organs and synthetic tissue scaffolds (containing cells) by way of the nutrient transport characteristics of hierarchical arterial/venous, biliary and lymphatic vascular trees in organs or labyrinthine pore structures within scaffolds. Our bioengineering goals are to broaden the range of gray-scale accuracy of x-ray mu CT so as to more quantitatively characterize the microarchitecture of the hierarchical and labyrinthine systems in terms of their transport of solutes and cells and their mechanical function within those intact organs and within synthetic tissue scaffolds. This will involve development/evaluation and use of software to analyze and model the imaged transport channels and to enhance the image information content with tunable monochromatic x-ray scans, x-ray scatter imaging and new x-ray contrast materials (e.g.. nano-particulate) which are indicators of transport into/out of specific vascular or pore spaces of interest and by extending our cryostatic micro-CT capability so that the diffusional & micro-convective dynamics of contrast agent distribution can be followed by snap-freezing the specimens.
AIM I : Characterize Solute Transport in Micro-Vascular """"""""Trees"""""""" & Tissue Scaffold Pore """"""""Labyrinths:"""""""" la) Segmentation & Dimensional geometry analysis of the """"""""trees"""""""" and """"""""labyrinths"""""""". Ib) Modeling of vascular """"""""tree"""""""" and pore """"""""Labyrinth"""""""" transport & transmission characteristics. Ic) Scaffold mechanical & pore transport properties relationship to tissue in-growth.
AIM II : Micro-CT using Multi Energy and Scattered X-ray: lla) Multi-energy monochromatic x-ray will be evaluated for better discrimination of pathologically and metabolically accumulating compounds and lib) x-ray scatter imaging will be used to determine preferred diffusion paths in tendons and muscle.
AIM III : Development & Evaluation of Nano-particulate Contrast Agent: Ilia) Biliary excretion and transport in polycystic liver disease. 1Mb) Lymph generation and transport.
AIM I V: Generate a Web-Accessible Micro-CT Image Data Base: Place 3D image data sets in a web accessible data base so as to provide a range of micro-anatomic features available in various organs.
AIM V : Develop an Image """"""""Data Mining"""""""" Capability. Since the vast volume of data available in a micro- CT data set presents a great challenge to interrogate, we will implement interactive computer-graphics techniques suitable for extracting useful quantitative information from these data sets. The biomedical significance of these aims is their contribution towards increased understanding of transport mechanisms within synthetic implants, tissues and arterial walls in early stages of arterial disease, within biliary ductules in polycystic hepatorenal disease and spread of cells in lymphatic trees. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB000305-10
Application #
7286064
Study Section
Biomedical Imaging Technology Study Section (BMIT)
Program Officer
Lopez, Hector
Project Start
1996-09-30
Project End
2010-07-31
Budget Start
2007-08-01
Budget End
2008-07-31
Support Year
10
Fiscal Year
2007
Total Cost
$557,087
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Moritz, Regina; Anderson, Jill L; Vercnocke, Andrew J et al. (2013) Changes in CT angiographic opacification of porcine coronary artery wall with patchy altered flow in vasa vasorum. Int J Cardiovasc Imaging 29:1325-33
Beighley, Patricia E; Zamir, Mair; Wentz, Robert J et al. (2013) Vascularity of myocardium and gastrocnemius muscle in rats selectively bred for endurance running capacity. Physiol Genomics 45:119-25
Masyuk, Tatyana V; Radtke, Brynn N; Stroope, Angela J et al. (2013) Pasireotide is more effective than octreotide in reducing hepatorenal cystogenesis in rodents with polycystic kidney and liver diseases. Hepatology 58:409-21
Sangaralingham, S Jeson; Ritman, Erik L; McKie, Paul M et al. (2012) Cardiac micro-computed tomography imaging of the aging coronary vasculature. Circ Cardiovasc Imaging 5:518-24
Masyuk, Tatyana V; Radtke, Brynn N; Stroope, Angela J et al. (2012) Inhibition of Cdc25A suppresses hepato-renal cystogenesis in rodent models of polycystic kidney and liver disease. Gastroenterology 142:622-633.e4
Hirata, Taku; Cabrero, Pablo; Berkholz, Donald S et al. (2012) In vivo Drosophilia genetic model for calcium oxalate nephrolithiasis. Am J Physiol Renal Physiol 303:F1555-62
Malyar, Nasser M; Lerman, Lilach O; Gossl, Mario et al. (2011) Relationship between surface area of nonperfused myocardium and extravascular extraction of contrast agent following coronary microembolization. Am J Physiol Regul Integr Comp Physiol 301:R430-7
Ritman, Erik L (2011) Current status of developments and applications of micro-CT. Annu Rev Biomed Eng 13:531-52
Han, Xiao; Bian, Junguo; Eaker, Diane R et al. (2011) Algorithm-enabled low-dose micro-CT imaging. IEEE Trans Med Imaging 30:606-20
Thabut, Dominique; Routray, Chittaranjan; Lomberk, Gwen et al. (2011) Complementary vascular and matrix regulatory pathways underlie the beneficial mechanism of action of sorafenib in liver fibrosis. Hepatology 54:573-85

Showing the most recent 10 out of 68 publications