Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury
Heterotopic ossification (HO) is the abnormal growth of bone in soft connective tissues that occurs as a frequent complication in individuals with traumatic brain injury (TBI) and in rare genetic disorders. Therefore, understanding the mechanisms behind ectopic bone formation in response to TBI is l...
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| Format: | Article |
| Language: | English |
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MDPI AG
2023-03-01
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| Series: | Biomedicines |
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| Online Access: | https://www.mdpi.com/2227-9059/11/3/943 |
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| author | Chandrasekhar Kesavan Gustavo A. Gomez Sheila Pourteymoor Subburaman Mohan |
| author_facet | Chandrasekhar Kesavan Gustavo A. Gomez Sheila Pourteymoor Subburaman Mohan |
| author_sort | Chandrasekhar Kesavan |
| collection | DOAJ |
| description | Heterotopic ossification (HO) is the abnormal growth of bone in soft connective tissues that occurs as a frequent complication in individuals with traumatic brain injury (TBI) and in rare genetic disorders. Therefore, understanding the mechanisms behind ectopic bone formation in response to TBI is likely to have a significant impact on identification of novel therapeutic targets for HO treatment. In this study, we induced repetitive mild TBI (mTBI) using a weight drop model in mice and then stimulated HO formation via a local injury to the Achilles tendon or fibula. The amount of ectopic bone, as evaluated by micro-CT analyses, was increased by four-fold in the injured leg of mTBI mice compared to control mice. However, there was no evidence of HO formation in the uninjured leg of mTBI mice. Since tissue injury leads to the activation of hypoxia signaling, which is known to promote endochondral ossification, we evaluated the effect of IOX2, a chemical inhibitor of PHD2 and a known inducer of hypoxia signaling on HO development in response to fibular injury. IOX2 treatment increased HO volume by five-fold compared to vehicle. Since pericytes located in the endothelium of microvascular capillaries are known to function as multipotent tissue-resident progenitors, we determined if activation of hypoxia signaling promotes pericyte recruitment at the injury site. We found that markers of pericytes, NG2 and PDGFRβ, were abundantly expressed at the site of injury in IOX2 treated mice. Treatment of pericytes with IOX2 for 72 h stimulated expression of targets of hypoxia signaling (<i>Vegf</i> and <i>Epo</i>), as well as markers of chondrocyte differentiation (<i>Col2α1</i> and <i>Col10α1</i>). Furthermore, serum collected from TBI mice was more effective in promoting the proliferation and differentiation of pericytes than control mouse serum. In conclusion, our data show that the hypoxic state at the injury site in soft tissues of TBI mice provides an environment leading to increased accumulation and activation of pericytes to form endochondral bone. |
| first_indexed | 2024-03-11T06:54:06Z |
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| institution | Directory Open Access Journal |
| issn | 2227-9059 |
| language | English |
| last_indexed | 2024-03-11T06:54:06Z |
| publishDate | 2023-03-01 |
| publisher | MDPI AG |
| record_format | Article |
| series | Biomedicines |
| spelling | doaj.art-fd6c3560563243db8a22054dab351c512023-11-17T09:47:53ZengMDPI AGBiomedicines2227-90592023-03-0111394310.3390/biomedicines11030943Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local InjuryChandrasekhar Kesavan0Gustavo A. Gomez1Sheila Pourteymoor2Subburaman Mohan3Musculoskeletal Disease Center, VA Loma Linda Healthcare System, Loma Linda, CA 92357, USAMusculoskeletal Disease Center, VA Loma Linda Healthcare System, Loma Linda, CA 92357, USAMusculoskeletal Disease Center, VA Loma Linda Healthcare System, Loma Linda, CA 92357, USAMusculoskeletal Disease Center, VA Loma Linda Healthcare System, Loma Linda, CA 92357, USAHeterotopic ossification (HO) is the abnormal growth of bone in soft connective tissues that occurs as a frequent complication in individuals with traumatic brain injury (TBI) and in rare genetic disorders. Therefore, understanding the mechanisms behind ectopic bone formation in response to TBI is likely to have a significant impact on identification of novel therapeutic targets for HO treatment. In this study, we induced repetitive mild TBI (mTBI) using a weight drop model in mice and then stimulated HO formation via a local injury to the Achilles tendon or fibula. The amount of ectopic bone, as evaluated by micro-CT analyses, was increased by four-fold in the injured leg of mTBI mice compared to control mice. However, there was no evidence of HO formation in the uninjured leg of mTBI mice. Since tissue injury leads to the activation of hypoxia signaling, which is known to promote endochondral ossification, we evaluated the effect of IOX2, a chemical inhibitor of PHD2 and a known inducer of hypoxia signaling on HO development in response to fibular injury. IOX2 treatment increased HO volume by five-fold compared to vehicle. Since pericytes located in the endothelium of microvascular capillaries are known to function as multipotent tissue-resident progenitors, we determined if activation of hypoxia signaling promotes pericyte recruitment at the injury site. We found that markers of pericytes, NG2 and PDGFRβ, were abundantly expressed at the site of injury in IOX2 treated mice. Treatment of pericytes with IOX2 for 72 h stimulated expression of targets of hypoxia signaling (<i>Vegf</i> and <i>Epo</i>), as well as markers of chondrocyte differentiation (<i>Col2α1</i> and <i>Col10α1</i>). Furthermore, serum collected from TBI mice was more effective in promoting the proliferation and differentiation of pericytes than control mouse serum. In conclusion, our data show that the hypoxic state at the injury site in soft tissues of TBI mice provides an environment leading to increased accumulation and activation of pericytes to form endochondral bone.https://www.mdpi.com/2227-9059/11/3/943repetitive mild TBImicetendon injuryhypoxiaheterotopic ossficationpericytes |
| spellingShingle | Chandrasekhar Kesavan Gustavo A. Gomez Sheila Pourteymoor Subburaman Mohan Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury Biomedicines repetitive mild TBI mice tendon injury hypoxia heterotopic ossfication pericytes |
| title | Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury |
| title_full | Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury |
| title_fullStr | Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury |
| title_full_unstemmed | Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury |
| title_short | Development of an Animal Model for Traumatic Brain Injury Augmentation of Heterotopic Ossification in Response to Local Injury |
| title_sort | development of an animal model for traumatic brain injury augmentation of heterotopic ossification in response to local injury |
| topic | repetitive mild TBI mice tendon injury hypoxia heterotopic ossfication pericytes |
| url | https://www.mdpi.com/2227-9059/11/3/943 |
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