Sonic Hedgehog-activated engineered blood vessels enhance bone tissue formation

Large bone defects naturally regenerate via a highly vascularized tissue which progressively remodels into cartilage and bone. Current approaches in bone tissue engineering are restricted by delayed vascularization and fail to recapitulate this stepwise differentiation toward bone tissue. Here, we use the morphogen Sonic Hedgehog (Shh) to induce the in vitro organization of an endothelial capillary network in an artificial tissue. We show that endogenous Hedgehog activity regulates angiogenic genes and the formation of vascular lumens. Exogenous Shh further induces the in vitro development of the vasculature (vascular lumen formation, size, distribution). Upon implantation, the in vitro development of the vasculature improves the in vivo perfusion of the artificial tissue and is necessary to contribute to, and enhance, the formation of de novo mature bone tissue. Similar to the regenerating callus, the artificial tissue undergoes intramembranous and endochondral ossification and forms a trabecular-like bone organ including bone-marrow-like cavities. These findings open the door for new strategies to treat large bone defects by closely mimicking natural endochondral bone repair.

[1]  M. Menger,et al.  Vascularization in Tissue Engineering: Angiogenesis versus Inosculation , 2012, European Surgical Research.

[2]  A. Landesberg,et al.  Improved vascular organization enhances functional integration of engineered skeletal muscle grafts , 2011, Proceedings of the National Academy of Sciences.

[3]  Ivan Martin,et al.  Recapitulation of endochondral bone formation using human adult mesenchymal stem cells as a paradigm for developmental engineering , 2010, Proceedings of the National Academy of Sciences.

[4]  T. Clemens,et al.  Role of HIF‐1α in skeletal development , 2010, Annals of the New York Academy of Sciences.

[5]  M. Kazanietz,et al.  Hedgehog proteins activate pro-angiogenic responses in endothelial cells through non-canonical signaling pathways , 2010, Cell cycle.

[6]  Douglas Losordo,et al.  Sonic hedgehog regulates angiogenesis and myogenesis during post‐natal skeletal muscle regeneration , 2009, Journal of cellular and molecular medicine.

[7]  M. Iruela-Arispe,et al.  Cellular and molecular mechanisms of vascular lumen formation. , 2009, Developmental cell.

[8]  C. V. van Blitterswijk,et al.  The use of endothelial progenitor cells for prevascularized bone tissue engineering. , 2009, Tissue engineering. Part A.

[9]  S. Warren,et al.  Hedgehog signaling is essential for normal wound healing , 2008, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[10]  I. Weissman,et al.  Endochondral ossification is required for hematopoietic stem cell niche formation , 2008, Nature.

[11]  Jeroen Rouwkema,et al.  Vascularization in tissue engineering. , 2008, Trends in biotechnology.

[12]  Joyce Doorn,et al.  cAMP/PKA pathway activation in human mesenchymal stem cells in vitro results in robust bone formation in vivo , 2008, Proceedings of the National Academy of Sciences.

[13]  Dai Fukumura,et al.  Bone marrow-derived mesenchymal stem cells facilitate engineering of long-lasting functional vasculature. , 2008, Blood.

[14]  F. Shapiro,et al.  Bone development and its relation to fracture repair. The role of mesenchymal osteoblasts and surface osteoblasts. , 2008, European cells & materials.

[15]  C. V. van Blitterswijk,et al.  Engineering vascularised tissues in vitro. , 2008, European cells & materials.

[16]  James Briscoe,et al.  Interpretation of the sonic hedgehog morphogen gradient by a temporal adaptation mechanism , 2007, Nature.

[17]  Clemens A van Blitterswijk,et al.  Cell-Based Bone Tissue Engineering , 2007, PLoS medicine.

[18]  J. Voncken,et al.  A novel in vivo model to study endochondral bone formation; HIF-1alpha activation and BMP expression. , 2007, Bone.

[19]  Rickard Sandberg,et al.  Improved precision and accuracy for microarrays using updated probe set definitions , 2007, BMC Bioinformatics.

[20]  Jeroen Rouwkema,et al.  Endothelial cells assemble into a 3-dimensional prevascular network in a bone tissue engineering construct. , 2006, Tissue engineering.

[21]  C. V. van Blitterswijk,et al.  Cross-species comparison of ectopic bone formation in biphasic calcium phosphate (BCP) and hydroxyapatite (HA) scaffolds. , 2006, Tissue engineering.

[22]  Jun Asai,et al.  Topical Sonic Hedgehog Gene Therapy Accelerates Wound Healing in Diabetes by Enhancing Endothelial Progenitor Cell–Mediated Microvascular Remodeling , 2006, Circulation.

[23]  Masaaki,et al.  Sonic hedgehog myocardial gene therapy: tissue repair through transient reconstitution of embryonic signaling , 2005, Nature Medicine.

[24]  C. Betsholtz,et al.  Endothelial/Pericyte Interactions , 2005, Circulation research.

[25]  D. Kohane,et al.  Engineering vascularized skeletal muscle tissue , 2005, Nature Biotechnology.

[26]  S. Vokes,et al.  Hedgehog signaling is essential for endothelial tube formation during vasculogenesis , 2004, Development.

[27]  B. Olsen,et al.  VEGFA is necessary for chondrocyte survival during bone development , 2004, Development.

[28]  Dai Fukumura,et al.  Tissue engineering: Creation of long-lasting blood vessels , 2004, Nature.

[29]  J. Isner,et al.  Postnatal Recapitulation of Embryonic Hedgehog Pathway in Response to Skeletal Muscle Ischemia , 2003, Circulation.

[30]  B. Guillotin,et al.  Effect of HUVEC on human osteoprogenitor cell differentiation needs heterotypic gap junction communication. , 2002, American journal of physiology. Cell physiology.

[31]  Takayuki Asahara,et al.  The morphogen Sonic hedgehog is an indirect angiogenic agent upregulating two families of angiogenic growth factors , 2001, Nature Medicine.

[32]  H. Augustin,et al.  Blood vessel maturation in a 3‐dimensional spheroidal coculture model: direct contact with smooth muscle cells regulates endothelial cell quiescence and abrogates VEGF responsiveness , 2001, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[33]  M. Scott,et al.  Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine , 2000, Nature.

[34]  S. Murakami,et al.  Expression of Indian Hedgehog During Fracture Healing in Adult Rat Femora , 2000, Calcified Tissue International.

[35]  Xing‐dong Zhang,et al.  Osteoinduction by calcium phosphate biomaterials , 1998, Journal of materials science. Materials in medicine.

[36]  J. Glowacki Angiogenesis in fracture repair. , 1998, Clinical orthopaedics and related research.

[37]  W. Birchmeier,et al.  Inhibitory action of transforming growth factor beta on endothelial cells. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[38]  Surajit Sinha,et al.  Purmorphamine activates the Hedgehog pathway by targeting Smoothened , 2006, Nature chemical biology.