for Histology Core The structure and composition of musculoskeletal tissues are tailored to meet their demanding functions. With injury, aging, and specific diseases, the structure and composition of these tissues deteriorate, resulting in a decline or loss of biological, phenotypic and mechanical function and properties. Musculoskeletal tissues each have a wide array of compositional and structural variety with respect to cellular components, microarchitecture, and extracellular matrix constituents. Careful description and quantification of tissue structural organization and composition, as well as localization and identification of secreted factors, are necessary requirements for elucidation of the biologic mechanisms underlying musculoskeletal integrity, injury, and repair. The overall objective of this Histology Core (HC) is to utilize and develop a wide range of standard and innovative histological and histomorphometric approaches to evaluate musculoskeletal tissue injury and repair, and to provide training and funding for new projects and collaborations utilizing these assays. There is an increasing demand for specialized histological techniques, development of new histomorphological methods, and customization of histological approaches to musculoskeletal-based problems. The need for these approaches is ever-broadening due to the recognition that many musculoskeletal disorders can affect other systems (indirectly, including muscle, bone, and other connective structures). In addition, some pathologies are true multisystem disorders that also affect musculoskeletal tissues. Thus, investigators whose interests were initially focused on non-musculoskeletal pathology now also require access to the advice and services provided by the HC. In addition, with the proliferation of new animal models, it is critical to be able to characterize their musculoskeletal phenotype, whether it is primarily or secondarily affected by a genetic disorder or other type of musculoskeletal insult. The HC of the Penn Center for Musculoskeletal Disorders (PCMD) has flourished under the leadership of Dr. Robert Pignolo, who has been Director since July 2010. Importantly, the home of HC is in Stemmler Hall, the same building as the other two Resource Cores and the Administrative Core, defining a clear home for the PCMD overall.
The Specific Aims of the HC are to: 1) To provide guidance and training on the capabilities, advantages, and disadvantages of the various methodologies to assess musculoskeletal tissue structure and composition through formal educational enrichment programs and one-on-one interactions, 2) To provide high-quality expertise and service for histological and histomorphometric assays of musculoskeletal tissues, 3) To develop new and innovative histologically-based techniques that will be applicable to musculoskeletal research, and 4) To provide funding for development of new projects and collaborations and to develop preliminary and/or feasibility data for investigators.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
1P30AR069619-01
Application #
9087467
Study Section
Special Emphasis Panel (ZAR1-XZ (M1))
Project Start
2016-07-01
Project End
2021-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
1
Fiscal Year
2016
Total Cost
$145,271
Indirect Cost
$55,040
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Sierra, Luz-Jeannette; Brown, Amy G; Barilá, Guillermo O et al. (2018) Colonization of the cervicovaginal space with Gardnerella vaginalis leads to local inflammation and cervical remodeling in pregnant mice. PLoS One 13:e0191524
Jia, Haoruo; Ma, Xiaoyuan; Wei, Yulong et al. (2018) Loading-Induced Reduction in Sclerostin as a Mechanism of Subchondral Bone Plate Sclerosis in Mouse Knee Joints During Late-Stage Osteoarthritis. Arthritis Rheumatol 70:230-241
Rooney, Sarah Ilkhanipour; Torino, Daniel J; Baskin, Rachel et al. (2018) Doxycycline improves cage activity, but not exercised, supraspinatus tendon and muscle in a rat model. J Biomech 80:79-87
Sambamurthy, Nisha; Zhou, Cheng; Nguyen, Vu et al. (2018) Deficiency of the pattern-recognition receptor CD14 protects against joint pathology and functional decline in a murine model of osteoarthritis. PLoS One 13:e0206217
Qu, Feini; Stoeckl, Brendan D; Gebhard, Peter M et al. (2018) A Wearable Magnet-Based System to Assess Activity and Joint Flexion in Humans and Large Animals. Ann Biomed Eng 46:2069-2078
Rajapakse, Chamith S; Kobe, Elizabeth A; Batzdorf, Alexandra S et al. (2018) Accuracy of MRI-based finite element assessment of distal tibia compared to mechanical testing. Bone 108:71-78
Gullbrand, Sarah E; Ashinsky, Beth G; Bonnevie, Edward D et al. (2018) Long-term mechanical function and integration of an implanted tissue-engineered intervertebral disc. Sci Transl Med 10:
Chandra, Abhishek; Wang, Luqiang; Young, Tiffany et al. (2018) Proteasome inhibitor bortezomib is a novel therapeutic agent for focal radiation-induced osteoporosis. FASEB J 32:52-62
Qu, Feini; Li, Qing; Wang, Xiao et al. (2018) Maturation State and Matrix Microstructure Regulate Interstitial Cell Migration in Dense Connective Tissues. Sci Rep 8:3295
Tichy, Elisia D; Sidibe, David K; Greer, Christopher D et al. (2018) A robust Pax7EGFP mouse that enables the visualization of dynamic behaviors of muscle stem cells. Skelet Muscle 8:27

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