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HHS Recovery Act Recipient Reporting Readiness Tool

Step 4. Review and Copy the Grant Awards Data

TAGGS provides some – but not all – of the data needed for the Recipient Report. Recipients are responsible for directly collecting and reporting all required data to FederalReporting.gov. Data that HHS does not currently collect are highlighted in yellow. Do not copy this highlighted information. Please enter the appropriate data for your organization in these required fields. For assistance with entering these data please contact FederalReporting.gov.

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Award Detail for: CHARACTERIZATION OF ENDOGENOUS STEM CELLS WITHIN ENDOSSEOUS WOUNDS
BRIGHAM & WOMEN`S HOSPITAL
DUNS Number: 030811269
10 VINING STREET
BOSTON, MA 02115-6114
Recipient Report: Grant or Loan
Prime Recipient

Reporting Information
Award Type Award Number Final Report
Grant 1R03DE019191-01A1 Recipient responsible for this data

Award Recipient Information
Recipient DUNS Number Recipient Account Number Recipient Congressional District
030811269 Recipient responsible for this data 8

Award Information
Funding Agency Code Awarding Agency Code Award Date
7529 7529 07-16-2009
Amount of Award Sub Account Number for Program Source (TAS)  
$ 129,250 Recipient responsible for this data
Program Source (TAS)* CFDA Number 
750874 93.701
Total Number of Sub Awards to Individuals Total Amount of Sub Awards to Individuals
Recipient responsible for this data Recipient responsible for this data
Total Number of Payments to Vendors less than $25,000/award Total Amount of Payments to Vendors less than $25,000/award
Recipient responsible for this data Recipient responsible for this data
Total Number of Sub Awards less than $25,000/award Total Amount of Sub Awards less than $25,000/award
Recipient responsible for this data Recipient responsible for this data
Award Description
DESCRIPTION (provided by applicant): Given the high incidence of bone trauma, cancer, and adult and congenital disease, which is associated with over 500,000 bone graft procedures each year in North America, it is not surprising that bone is the most common transplanted tissue, second only to blood. In addition to traditional bone grafting for defects, there are numerous clinical applications that can benefit from bone regeneration therapies including temporomandibular joint reconstruction to alleviate jaw pain which affects an estimated 90 million Americans, and restoration of contour and shape within reconstructed craniofacial bone. Mesenchymal stem and progenitor cells (MSPCs) are believed to play an important role during bone regeneration, however very little is known regarding their invasion into damaged or diseased tissue. To date there are no studies that examine the temporal and spatial distribution of endogenous mesenchymal stem and progenitor cells (MSPCs) during endosseous wound regeneration. Such characterization may be critical to developing therapeutic strategies that rely on recruitment of these cells (i.e., via delivery of growth factors) or the use of an exogenous source of stem or progenitor cells. Additionally, the impact of implanting or injecting scaffolds or hydrogel matrices on the migration and differentiation of MSPCs is unknown. Here we aim to characterize the spatial-temporal profile of endogenous MSPC migration and differentiation within defects that regenerate at different rates that will facilitate the creation of a core animal model for our laboratory. This will be used to interrogate various pathways involving MSPCs in regeneration of damaged or diseased bone tissue. AIM 1: To characterize the spatial and temporal aspects of MSPC migration and differentiation during endosseous wound healing within non-critical size defects. This will be accomplished through first validating antibodies in vitro with purified populations of MSPCs, followed by immunohistochemical analysis of MSPC migration and differentiation within a rat non-critical sized endosseous defect. AIM 2: To determine if the spatial-temporal migration and differentiation of endogenous MSPCs changes upon implantation of biomaterial matrices which significantly delay bone regeneration. Public Health Relevance: Existing clinical strategies for regeneration of craniofacial bone defects including functional deficits and severe aesthetic deformities are fraught with many limitations. We aim to characterize the spatial-temporal profile of endogenous mesenchymal stem and progenitor cell migration and differentiation within defects that regenerate at different rates. This will facilitate the creation of a core animal model that we can use to develop new strategies for enhancing bone regeneration based on harnessing the regenerative capacity of mesenchymal stem cells.

Project Information
Project Name or
Project/Program Title
Project Status Total Federal Amount ARRA Funds
Received/Invoiced
CHARACTERIZATION OF ENDOGENOUS STEM CELLS WITHIN ENDOSSEOUS WOUNDS Recipient responsible for this data Recipient responsible for this data
Number of Jobs Description of Jobs Created
Recipient responsible for this data Recipient responsible for this data
Quarterly Activities/Project Description
Recipient responsible for this data
 
Activity Code (NAICS or NTEE-NPC)
1Recipient responsible for this data2Recipient responsible for this data
3Recipient responsible for this data4Recipient responsible for this data
5Recipient responsible for this data6Recipient responsible for this data
7Recipient responsible for this data8Recipient responsible for this data
9Recipient responsible for this data10Recipient responsible for this data
Total Federal Amount of ARRA
Expenditure
Total Federal ARRA
Infrastructure Expenditure
Infrastructure Contact Name
Recipient responsible for this data Recipient responsible for this data Recipient responsible for this data
Infrastructure Contact Email Infrastructure Contact Phone Infrastructure Contact Phone Ext.
Recipient responsible for this data Recipient responsible for this data Recipient responsible for this data
Infrastructure Contact Street Address 1 Infrastructure Contact Street Address 2 Infrastructure Contact Street Address 3
10 VINING STREET Not Available Recipient responsible for this data
Infrastructure City Infrastructure State Infrastructure ZIP Code+4
BOSTON MA 02115-6114
Infrastructure Purpose and Rationale
Recipient responsible for this data

Primary Place of Performance
Street Address 1 Street Address 2 City
RESEARCH ADMINISTRATION 75 FRANCIS ST Recipient responsible for this data BOSTON
State Zip Code+4 Congressional District
MA 2115 Not Available
Country  
US

Recipient Highly Compensated Officers
Prime Recipient Indication of Reporting Applicability # Officer Name Officer Compensation
Recipient responsible for this data 1 Recipient responsible for this data Recipient responsible for this data
2 Recipient responsible for this data Recipient responsible for this data
3 Recipient responsible for this data Recipient responsible for this data
4 Recipient responsible for this data Recipient responsible for this data
5 Recipient responsible for this data Recipient responsible for this data

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USE IN THE RECIPIENT REPORT

The information provided by this tool is baseline data that the Recipient should include in the Recipient Report that must be submitted to FederalReporting.gov beginning October 1, 2009. The data from this tool can be cut and pasted directly into the Recipient Report.