GENE EXPRESSION PROFILING IN THE NERVOUS SYSTEM FOLLOWING TRAUMATIC SPINAL
CORD INJURY
Release Date: February 16, 2001
NOTICE: NOT-NS-01-006
NATIONAL INSTITUE OF NEUROLOGICAL DISORDERS AND STROKE (NINDS)
REQUEST FOR PROPOSAL (RFP): NIH-NINDS-01-03
The National Institute of Neurological Disorders and Stroke (NINDS), NIH
announces the availability of a Broad Agency Announcement (BAA) to support gene
expression profiling in the nervous system following traumatic spinal cord
injury (SCI).
Research on animal models of SCI have provided insights into the complexity of
the injury, the many stages of cellular damage and recovery, and the complexity
of approaches that will be necessary to address treatment and rehabilitation.
Research efforts will employ neural tissue-specific and/or species-specific
reagents and contemporary high throughput methodologies to quantify expression
profiles of genes in acute and chronic phases of SCI. Changes in expression
will be characterized at the injury site as well as in areas of the cord rostral
and caudal to the lesion site. In addition, regions of brain that represent
areas that project to or receive input from the spinal cord will be evaluated
for alterations in gene expression. The injury paradigm will utilize
well-characterized and justified rodent models of spinal cord trauma. Since the
areas sampled are complex structures, patterns of expression of specific genes
will be characterized on a cellular/tissue level. Analysis of the multitudes of
altered proteins after injury is a daunting task. Up until now, investigators
have studied particular molecules (i.e., GAP-43, NOGO) or classes of proteins
(i.e., cytoskeletal proteins, trophic factors) in the hope of finding evidence
for involvement in either regenerative or inhibitory responses. The development
of new technologies to screen large numbers of genes (or specific sequences) for
expression after injury may focus the search for the critical elements.
Obviously, a complex condition such as SCI has critical temporal and anatomic
parameters. Prevention of outgrowth may occur at the injured axon tip or at the
cell body. Negative or positive factors are likely expressed from the time of
the injury through several stages of recovery and stabilization. Therefore,
analysis should include comparative time frames after trauma, and various parts
of the neuroaxis that may react differently to the injury, regeneration or
stabilization phases. The purpose of this BAA is to utilize new gene screening
processes in order to determine temporal and regional changes in expression of a
large number of genes following traumatic SCI. From this data, certain
specified genes will be subsequently analyzed for post-injury changes in
patterns and localization of their expression. This two-step process will allow
for a large scale screening of potential genes that are changed after SCI as
well as a more focused study of genes that are determined to be important to
injury and potential regenerative processes. High throughput data obtained from
these experiments will become part of a public database for dissemination to the
scientific community.
Prospective offerors are expected to have personnel resources adequate to
conduct the proposed research with expertise in the following areas: SCI animal
models and basic research, molecular genetics, array technology, and
bioinformatics. Prospective offerors are also expected to have access to
facilities (either on-site or through collaborative relationships) adequate to
conduct the research such as: DNA microarray or other gene expression
research facilities.
It is anticipated that one (1) cost-reimbursement type contracts may be awarded
for a maximum period of up to three years. BAA/Request for Proposals (RFP) No.
NIH-NINDS-01-03 will be AVAILABLE ELECTRONICALLY and may be downloaded at URL
http://www.ninds.nih.gov/funding/funding_announcements/RFP_all.htm on or about March 1, 2001.
This solicitation will be issued in electronic format only. Proposals will be
due on or about May 10, 2001. The exact proposal receipt date will be specified
in the solicitation. OFFERORS ARE RESPONSIBLE FOR ROUTINELY CHECKING THIS
WEBSITE FOR ANY POSSIBLE SOLICITATION AMENDMENTS THAT MAY BE ISSUED. NO
INDIVIDUAL NOTIFICATION OF ANY AMENDMENTS WILL BE PROVIDED. This advertisement
does not commit the Government to award a contract. All responsible sources may
submit a proposal, which will be considered by the agency. See Note 26. *****
Inquiries may be directed to:
Laurie A. Leonard, Contracting Officer
Contracts Management Branch
National Institute of Neurological Disorders and Stroke
Neuroscience Center, Room 3287
6001 Executive Boulevard, MSC 9531
Bethesda, MD 20892-9531
Tel: (301) 496-1813
Fax: (301) 402-4225
Email: [email protected]
Weekly TOC for this Announcement
NIH Funding Opportunities and Notices
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