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04.05.2024 | Original Article

Plasminogen activator inhibitor-1 is involved in glucocorticoid-induced decreases in angiogenesis during bone repair in mice

verfasst von: Kiyotaka Okada, Yuto Niwa, Kazusa Fukuhara, Takashi Ohira, Yuya Mizukami, Naoyuki Kawao, Osamu Matsuo, Hiroshi Kaji

Erschienen in: Journal of Bone and Mineral Metabolism

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Abstract

Introduction

Glucocorticoids delay fracture healing and induce osteoporosis. Angiogenesis plays an important role in bone repair after bone injury. Plasminogen activator inhibitor-1 (PAI-1) is the principal inhibitor of plasminogen activators and an adipocytokine that regulates metabolism. However, the mechanisms by which glucocorticoids delay bone repair remain unclear.

Materials and methods

Therefore, we herein investigated the roles of PAI-1 and angiogenesis in glucocorticoid-induced delays in bone repair after femoral bone injury using PAI-1-deficient female mice intraperitoneally administered dexamethasone (Dex).

Results

PAI-1 deficiency significantly attenuated Dex-induced decreases in the number of CD31-positive vessels at damaged sites 4 days after femoral bone injury in mice. PAI-1 deficiency also significantly ameliorated Dex-induced decreases in the number of CD31- and endomucin-positive type H vessels and CD31-positive- and endomucin-negative vessels at damaged sites 4 days after femoral bone injury. Moreover, PAI-1 deficiency significantly mitigated Dex-induced decreases in the expression of vascular endothelial growth factor as well as hypoxia inducible factor-1α, transforming growth factor-β1, and bone morphogenetic protein-2 at damaged sites 4 days after femoral bone injury.

Conclusion

The present results demonstrate that Dex-reduced angiogenesis at damaged sites during the early bone-repair phase after femoral bone injury partly through PAI-1 in mice.
Literatur
1.
Zurück zum Zitat Hofbauer LC, Minireview M, Rauner A (2009) Live and let die: molecular effects of glucocorticoids on bone cells. Mol Endocrinol 10:1525–1531CrossRef Hofbauer LC, Minireview M, Rauner A (2009) Live and let die: molecular effects of glucocorticoids on bone cells. Mol Endocrinol 10:1525–1531CrossRef
2.
Zurück zum Zitat McInnes IB, Schett G (2011) The pathogenesis of rheumatoid arthritis. N Engl J Med 365:2205–2219CrossRefPubMed McInnes IB, Schett G (2011) The pathogenesis of rheumatoid arthritis. N Engl J Med 365:2205–2219CrossRefPubMed
3.
Zurück zum Zitat Rhen T, Cidlowski JA (2005) Antiinflammatory action of glucocorticoids–new mechanisms for old drugs. N Engl J Med 353:1711–1723CrossRefPubMed Rhen T, Cidlowski JA (2005) Antiinflammatory action of glucocorticoids–new mechanisms for old drugs. N Engl J Med 353:1711–1723CrossRefPubMed
4.
Zurück zum Zitat Strehl C, Buttgereit F (2013) Optimized glucocorticoid therapy: teaching old drugs new tricks. Mol Cell Endocrinol 380:32–40CrossRefPubMed Strehl C, Buttgereit F (2013) Optimized glucocorticoid therapy: teaching old drugs new tricks. Mol Cell Endocrinol 380:32–40CrossRefPubMed
5.
Zurück zum Zitat Hachemi Y, Rapp AE, Picke AK, Weidinger G, Ignatius A, Tuckermann J (2018) Molecular mechanisms of glucocorticoids on skeletal and bone regeneration after fracture. J Mol Endocrinol 61:R75-90CrossRefPubMedPubMedCentral Hachemi Y, Rapp AE, Picke AK, Weidinger G, Ignatius A, Tuckermann J (2018) Molecular mechanisms of glucocorticoids on skeletal and bone regeneration after fracture. J Mol Endocrinol 61:R75-90CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Henneicke H, Gasparini SJ, Brennan-Speranza TC, Zhou H, Seibel MJ (2014) Glucocorticoids and bone: local effects and systemic implications. Trends Endocrinol Metab 25:197–211CrossRefPubMed Henneicke H, Gasparini SJ, Brennan-Speranza TC, Zhou H, Seibel MJ (2014) Glucocorticoids and bone: local effects and systemic implications. Trends Endocrinol Metab 25:197–211CrossRefPubMed
7.
Zurück zum Zitat Moutsatsou P, Kassi E, Papavassiliou AG (2012) Glucocorticoid receptor signaling in bone cells. Trends Mol Med 18:348–359CrossRefPubMed Moutsatsou P, Kassi E, Papavassiliou AG (2012) Glucocorticoid receptor signaling in bone cells. Trends Mol Med 18:348–359CrossRefPubMed
8.
Zurück zum Zitat Okada K, Okamoto T, Okumoto K, Takafuji Y, Ishida M, Kawao N, Matsuo O, Kaji H (2020) PAI-1 is involved in delayed bone repair induced by glucocorticoids in mice. Bone 134:115310CrossRefPubMed Okada K, Okamoto T, Okumoto K, Takafuji Y, Ishida M, Kawao N, Matsuo O, Kaji H (2020) PAI-1 is involved in delayed bone repair induced by glucocorticoids in mice. Bone 134:115310CrossRefPubMed
9.
Zurück zum Zitat Okada K, Kawao N, Nakai D, Wakabayashi R, Horiuchi Y, Okumoto K, Kurashimo S, Takafuji Y, Matsuo O, Kaji H (2022) Role of macrophages and plasminogen activator inhibitor-1 in delayed bone repair induced by glucocorticoids in mice. Int J Mol Sci 23:478CrossRefPubMedPubMedCentral Okada K, Kawao N, Nakai D, Wakabayashi R, Horiuchi Y, Okumoto K, Kurashimo S, Takafuji Y, Matsuo O, Kaji H (2022) Role of macrophages and plasminogen activator inhibitor-1 in delayed bone repair induced by glucocorticoids in mice. Int J Mol Sci 23:478CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Chen M, Li Y, Huang X, Gu Y, Li S, Yin P, Zhang L, Tang P (2021) Skeleton-vasculature chain reaction: a novel insight into the mystery of homeostasis. Bone Res 9:21CrossRefPubMedPubMedCentral Chen M, Li Y, Huang X, Gu Y, Li S, Yin P, Zhang L, Tang P (2021) Skeleton-vasculature chain reaction: a novel insight into the mystery of homeostasis. Bone Res 9:21CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Claes L, Recknagel S, Ignatius A (2012) Fracture healing under healthy and inflammatory conditions. Nat Rev Rheumatol 8:133–143CrossRefPubMed Claes L, Recknagel S, Ignatius A (2012) Fracture healing under healthy and inflammatory conditions. Nat Rev Rheumatol 8:133–143CrossRefPubMed
12.
Zurück zum Zitat Bahney CS, Zondervan RL, Allison P, Theologis A, Ashley JW, Ahn J, Miclau T, Marcuclo RS, Hankenson AD (2019) Cellular biology of fracture healing. J Orthop Res 37:35–50CrossRefPubMed Bahney CS, Zondervan RL, Allison P, Theologis A, Ashley JW, Ahn J, Miclau T, Marcuclo RS, Hankenson AD (2019) Cellular biology of fracture healing. J Orthop Res 37:35–50CrossRefPubMed
13.
Zurück zum Zitat Fusumbe AP, Ramasamy SK, Adams RH (2014) Coupling of angiogenesis and osteogenesis by a apecific vessel stbtype in bone. Nature 507:323–328CrossRef Fusumbe AP, Ramasamy SK, Adams RH (2014) Coupling of angiogenesis and osteogenesis by a apecific vessel stbtype in bone. Nature 507:323–328CrossRef
14.
15.
Zurück zum Zitat Kawao N, Tamura Y, Okumoto K, Yano M, Okada K, Matsuo O, Kaji H (2013) Plasminogen plays a crucial role in bone repair. J Bone Miner Res 28:1561–1574CrossRefPubMed Kawao N, Tamura Y, Okumoto K, Yano M, Okada K, Matsuo O, Kaji H (2013) Plasminogen plays a crucial role in bone repair. J Bone Miner Res 28:1561–1574CrossRefPubMed
16.
Zurück zum Zitat Kawao N, Tamura Y, Okumoto K, Yano M, Okada K, Matsuo O, Kaji H (2014) Tissue-type plasminogen activator deficiency delays bone repair: roles of osteoblast proliferation and vascular endothelial growth factor. Am J Physiol Endocrinol Metab 307:E278–E288CrossRefPubMed Kawao N, Tamura Y, Okumoto K, Yano M, Okada K, Matsuo O, Kaji H (2014) Tissue-type plasminogen activator deficiency delays bone repair: roles of osteoblast proliferation and vascular endothelial growth factor. Am J Physiol Endocrinol Metab 307:E278–E288CrossRefPubMed
17.
Zurück zum Zitat Kawao N, Tamura Y, Horiuchi Y, Okumoto K, Yano M, Okada K, Matsuo O, Kaji H (2015) The tissue fibrinolytic system contributes to the induction of macrophage function and CCL3 during bone repair in mice. PLoS ONE 10:e012398CrossRef Kawao N, Tamura Y, Horiuchi Y, Okumoto K, Yano M, Okada K, Matsuo O, Kaji H (2015) The tissue fibrinolytic system contributes to the induction of macrophage function and CCL3 during bone repair in mice. PLoS ONE 10:e012398CrossRef
18.
Zurück zum Zitat Okada K, Kawao N, Tatsumi K, Ishida M, Takafuji Y, Kurashimo S, Okumoto K, Kojima K, Matsuo O, Kaji H (2018) Roles of plasminogen in the alterations in bone marrow hematopoietic stem cells during bone repair. Bone Reports 8:195–203CrossRefPubMedPubMedCentral Okada K, Kawao N, Tatsumi K, Ishida M, Takafuji Y, Kurashimo S, Okumoto K, Kojima K, Matsuo O, Kaji H (2018) Roles of plasminogen in the alterations in bone marrow hematopoietic stem cells during bone repair. Bone Reports 8:195–203CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Kaji H (2016) Adipose tissue-derived plasminogen activator inhibitor-I function and regulation. Comp Physiol 6:1873–1896CrossRef Kaji H (2016) Adipose tissue-derived plasminogen activator inhibitor-I function and regulation. Comp Physiol 6:1873–1896CrossRef
20.
Zurück zum Zitat Mao L, Kawao N, Tamura Y, Okumoto K, Okada K, Yano M, Matsuo O, Kaji H (2014) Plasminogen activator inhibitor-1 is involved in impaired bone repair associated with diabetes in female mice. PLoS ONE 9:e92686CrossRefPubMedPubMedCentral Mao L, Kawao N, Tamura Y, Okumoto K, Okada K, Yano M, Matsuo O, Kaji H (2014) Plasminogen activator inhibitor-1 is involved in impaired bone repair associated with diabetes in female mice. PLoS ONE 9:e92686CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Tamura Y, Kawao N, Okada K, Yano M, Okumoto K, Matsuo O, Kaji H (2013) Plasminogen activator inhibitor-1 is involved in streptozotocin-induced bone loss in female mice. Diabetes 62:3170–3179CrossRefPubMedPubMedCentral Tamura Y, Kawao N, Okada K, Yano M, Okumoto K, Matsuo O, Kaji H (2013) Plasminogen activator inhibitor-1 is involved in streptozotocin-induced bone loss in female mice. Diabetes 62:3170–3179CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Mao L, Tamura Y, Kawao N, Okada K, Yano M, Okumoto K, Kaji H (2014) Influence of diabetic state and vitamin D deficiency on bone repair in female mice. Bone 61:102–108CrossRefPubMed Mao L, Tamura Y, Kawao N, Okada K, Yano M, Okumoto K, Kaji H (2014) Influence of diabetic state and vitamin D deficiency on bone repair in female mice. Bone 61:102–108CrossRefPubMed
23.
Zurück zum Zitat Schipani E, Maes C, Carmeliet G, Semenza GL (2009) Regulation of osteogenesis-angiogenesis coupling by HIFs and VEGF. J Bone Miner Res 24:1347–1353CrossRefPubMedPubMedCentral Schipani E, Maes C, Carmeliet G, Semenza GL (2009) Regulation of osteogenesis-angiogenesis coupling by HIFs and VEGF. J Bone Miner Res 24:1347–1353CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat Deckers MM, van Bezooijen RL, van der Horst G, Hoogendam J, van Der Bent C, Papapoulos SE, Lowik CW (2002) Bone morphogenetic proteins stimulate angiogenesis through osteoblast-derived vascular endothelial growth factor A. Endocrinology 143:1545–1553CrossRefPubMed Deckers MM, van Bezooijen RL, van der Horst G, Hoogendam J, van Der Bent C, Papapoulos SE, Lowik CW (2002) Bone morphogenetic proteins stimulate angiogenesis through osteoblast-derived vascular endothelial growth factor A. Endocrinology 143:1545–1553CrossRefPubMed
25.
Zurück zum Zitat Bostrom K, Zebboudj AF, Yao Y, Lin TS, Torres A, Matrix GL (2004) A protein stimulates VEGF expression through increased transforming growth factor-beta1 activity in endothelial cells. J Biol Chem 279:52904–52913CrossRefPubMed Bostrom K, Zebboudj AF, Yao Y, Lin TS, Torres A, Matrix GL (2004) A protein stimulates VEGF expression through increased transforming growth factor-beta1 activity in endothelial cells. J Biol Chem 279:52904–52913CrossRefPubMed
26.
Zurück zum Zitat Clifford RL, Deacon K, Knox AJ (2008) Novel regulation of vascular endothelial growth factor-A (VEGF-A) by transforming growth factor β1: requirement for Smads, β-catenin, and GSK3β. J Biol Chem 283:35337–35353CrossRefPubMed Clifford RL, Deacon K, Knox AJ (2008) Novel regulation of vascular endothelial growth factor-A (VEGF-A) by transforming growth factor β1: requirement for Smads, β-catenin, and GSK3β. J Biol Chem 283:35337–35353CrossRefPubMed
27.
Zurück zum Zitat Langen UH, Pitulescu ME, Kim JM, Enriquez-Gasca R, Sivaraj KK, Kusumbe AP, Singh A, Di Russo J, Bixel MG, Zhou B, Sorokin L, Vaquerizas JM, Adams RH (2017) Cell-matrix signals specify bone endothelial cells during developmental osteogenesis. Nat Cell Biol 19:189–201CrossRefPubMedPubMedCentral Langen UH, Pitulescu ME, Kim JM, Enriquez-Gasca R, Sivaraj KK, Kusumbe AP, Singh A, Di Russo J, Bixel MG, Zhou B, Sorokin L, Vaquerizas JM, Adams RH (2017) Cell-matrix signals specify bone endothelial cells during developmental osteogenesis. Nat Cell Biol 19:189–201CrossRefPubMedPubMedCentral
29.
Zurück zum Zitat Ramasamy SK, Kusumbe AP, Itkin T, Gur-Cohen S, Lapidot T, Adams RH (2016) Regulation of hematopoiesis and osteogenesis by blood vessel-derived signals. Annu Rev Cell Dev Biol 32:649–675CrossRefPubMed Ramasamy SK, Kusumbe AP, Itkin T, Gur-Cohen S, Lapidot T, Adams RH (2016) Regulation of hematopoiesis and osteogenesis by blood vessel-derived signals. Annu Rev Cell Dev Biol 32:649–675CrossRefPubMed
31.
Zurück zum Zitat Peng Y, Shan L, Yusheng L, Jianxi Z, Shijie C, Gehua Z, Xu C, Song W, Janet LC (2020) Glucocorticoids disrupt skeletal angiogenesis through transrepression of NF-κB–mediated preosteoclast Pdgfb transcription in young mice. J Bone Miner Res 35:1188–1202CrossRefPubMed Peng Y, Shan L, Yusheng L, Jianxi Z, Shijie C, Gehua Z, Xu C, Song W, Janet LC (2020) Glucocorticoids disrupt skeletal angiogenesis through transrepression of NF-κB–mediated preosteoclast Pdgfb transcription in young mice. J Bone Miner Res 35:1188–1202CrossRefPubMed
32.
Zurück zum Zitat Xie H, Cui Z, Wang L, Xia Z, Hu Y et al (2014) PDGF-BB secreted by preosteoclasts induces angiogenesis during coupling with osteogenesis. Nat Med 20:1270–2127CrossRefPubMedPubMedCentral Xie H, Cui Z, Wang L, Xia Z, Hu Y et al (2014) PDGF-BB secreted by preosteoclasts induces angiogenesis during coupling with osteogenesis. Nat Med 20:1270–2127CrossRefPubMedPubMedCentral
33.
Zurück zum Zitat Kohara Y, Kitazawa R, Haraguchi R, Imai Y, Kitazawa S, Kaji H (2016) Macrophages are requisite for angiogenesis of type H vessels during bone regeneration in mice. Bone 154:116200CrossRef Kohara Y, Kitazawa R, Haraguchi R, Imai Y, Kitazawa S, Kaji H (2016) Macrophages are requisite for angiogenesis of type H vessels during bone regeneration in mice. Bone 154:116200CrossRef
34.
Zurück zum Zitat Harada K, Yahata T, Onizuka M, Ibrahim AA, Kikkawa E, Miyata T, Ando K (2021) Plasminogen activator inhibitor type-1 is a negative regulator of hematopoietic regeneration in the adipocyte-rich bone marrow microenvironment. Biochem Biophys Res Commun 557:180–186CrossRefPubMed Harada K, Yahata T, Onizuka M, Ibrahim AA, Kikkawa E, Miyata T, Ando K (2021) Plasminogen activator inhibitor type-1 is a negative regulator of hematopoietic regeneration in the adipocyte-rich bone marrow microenvironment. Biochem Biophys Res Commun 557:180–186CrossRefPubMed
Metadaten
Titel
Plasminogen activator inhibitor-1 is involved in glucocorticoid-induced decreases in angiogenesis during bone repair in mice
verfasst von
Kiyotaka Okada
Yuto Niwa
Kazusa Fukuhara
Takashi Ohira
Yuya Mizukami
Naoyuki Kawao
Osamu Matsuo
Hiroshi Kaji
Publikationsdatum
04.05.2024
Verlag
Springer Nature Singapore
Erschienen in
Journal of Bone and Mineral Metabolism
Print ISSN: 0914-8779
Elektronische ISSN: 1435-5604
DOI
https://doi.org/10.1007/s00774-024-01510-w

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