Comprehensive functional phenotyping of trigeminal neurons innervating temporomandibular joint (TMJ) tissues in male female and aged mice primates and humans with and without TMJ disorders (tmjd) -…
Active Cooperative Agreement Awarded Last action
- Award ID
- UC2AR082195
- Recipient
-
The University Of Texas Health Science Center At San Antonio UEI C3KXNLTAAY98 Part of University Of Texas System
- Awarding agency
-
National Insititue of Arthritis and Musculoskeletal and Skin Diseases
National Institutes of Health, Department of Health and Human Services
- Obligated
- $29,011,491
Award facts
- Assistance listing
- 93.279 Drug Use and Addiction Research Programs
- Completion date 84% complete
- Originally
- Funding
-
- $24,313,389.00 Federal
- $4,698,102.00 Non-federal
- Funding agency
- National Institute of Neurological Disorders and Stroke National Institutes of Health, Department of Health and Human Services
- Place of performance
- San Antonio, TX 78229, USA
Award details come from USAspending.gov.
Description
Comprehensive functional phenotyping of trigeminal neurons innervating temporomandibular joint (TMJ) tissues in male female and aged mice primates and humans with and without TMJ disorders (tmjd) - the knowledge of the function, types, distributions, and plasticity of afferent neurites innervating temporomandibular joint (TMJ) tissues is needed to understand the underlying mechanisms controlling the development of temporomandibular joint disorder (tmjd) pain. The objective of this proposal is to address this critical GAP in knowledge by comprehensively elucidating the functions, types, neuroanatomical distributions, and plasticity of trigeminal (TG) neurons innervating the muscles, tendons, and fascia of the masseter (MM) and lateral pterygoid (LPM) muscles, as well as the cartilage, joint capsule, and ligament around TMJ condyle in male, female and aged mice, primates, and humans with and without tmjd pain conditions. In support of this proposal, we have demonstrated that TMJ tissues are innervated by trigeminal (TG) neurons with unique and distinct properties, distributions and molecular signatures compared to previously described TG and dorsal root ganglia (DRG) neurons. Based on supporting data and the expertise of our multi-disciplinary team, we anticipate that this project will map the location and elucidate the phenotype and plasticity for TG neurons innervating TMJ tissues in male, female, and aged mice, primates and humans with and without tmjd pain conditions. We also expect candidate therapeutic target identification in tmjd patients' TMJ tissues, which could ultimately lead to possible new treatments for tmjd. This study will be conducted in four interconnected yet independent aims. Aim 1 identifies the molecular signature, function and plasticity of TG neurons innervating TMJ tissues in male, female and aged mice with and without tmjd. Aim 2 maps afferent neurites innervating TMJ tissues in mice with and without tmjd. Aim 3 maps the location of neurites and define the phenotype and plasticity of TG neurons innervating TMJ tissues in non-human primates (NHP) with and without tmjd. Aim 4 examines TMJ tissue nerves and cell plasticity in tmjd patients. Substantial amount of data generated by this work will have a substantial positive impact by achieving most objectives of the RE-join program, including (1) mapping the location of the afferent neurites in TMJ tissues; (2) phenotyping and functionally characterizing TG neurons innervating a variety of TMJ tissues; (3) identifying tmjd-induced plasticity of these TG neurons in male, female and aged mice, primates and humans; (4) identifying novel candidate therapeutic targets in biopsies from tmjd patients; and (5) increasing study translatability by validating data from tmjd mouse models in primate and human tissues. The proposed experiments will create large, integrated, annotated datasets and metadata and develop advanced approaches, which will be shared with the research community conducting similar studies.
Transactions
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| Original award | $4,698,102 | $0 |
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Subawards
| Subrecipient | Amount | Awarded |
|---|---|---|
| University Of New Mexico | $296,031 | |
| Karolinska Institutet | $279,997 | |
| The University Of Texas At San Antonio | $565,608 | |
| The University Of Texas At San Antonio | $231,953 | |
| Wake Forest University Health Sciences | $92,793 | |
| Karolinska Institutet | $56,627 | |
| Karolinska Institutet | $263,373 | |
| Wake Forest University Health Sciences | $30,660 | |
| Wake Forest University Health Sciences | $160,000 | |
| The University Of Texas At San Antonio | $260,000 | |
| University Of Texas Medical Branch At Galveston | $135,000 | |
| University Of Texas Medical Branch At Galveston | $135,000 | |
| University Of Texas Medical Branch At Galveston | $160,000 | |
| The University Of Texas At San Antonio | $260,000 | |
| Wake Forest University Health Sciences | $185,000 |
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Quick answers
Who received award UC2AR082195?
UC2AR082195 was awarded to The University Of Texas Health Science Center At San Antonio by National Insititue of Arthritis and Musculoskeletal and Skin Diseases (National Institutes of Health) on September 23, 2022.
How much is award UC2AR082195 worth?
$29,011,491 has been obligated on UC2AR082195: $24,313,389 in federal funding and $4,698,102 in non-federal funding.
Which agency awarded UC2AR082195?
National Insititue of Arthritis and Musculoskeletal and Skin Diseases (National Institutes of Health) awarded UC2AR082195, with funding from National Institute of Neurological Disorders and Stroke (National Institutes of Health).
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