BMP9 stimulates joint regeneration at digit amputation wounds in mice

A major goal of regenerative medicine is to stimulate tissue regeneration after traumatic injury. We previously discovered that treating digit amputation wounds with BMP2 in neonatal mice stimulates endochondral ossification to regenerate the stump bone. Here we show that treating the amputation wound with BMP9 stimulates regeneration of a synovial joint that forms an articulation with the stump bone. Regenerated structures include a skeletal element lined with articular cartilage and a synovial cavity, and we demonstrate that this response requires the Prg4 gene. Combining BMP2 and BMP9 treatments in sequence stimulates the regeneration of bone and joint. These studies provide evidence that treatment of growth factors can be used to engineer a regeneration response from a non-regenerating amputation wound.Mammalian joints have poor regenerative capacity following amputation. Here, the authors show that in mice, stimulation of the amputation wound with BMP2 and BMP9 stimulates regeneration of a synovial joint that includes bone, cartilage and a synovial cavity.

[1]  Wei Li,et al.  Regulation of the ALK1 ligands, BMP9 and BMP10. , 2016, Biochemical Society transactions.

[2]  F. Barry,et al.  Distribution of cartilage molecules in the developing mouse joint. , 1999, Matrix biology : journal of the International Society for Matrix Biology.

[3]  Han Liu,et al.  The zinc finger transcription factors Osr1 and Osr2 control synovial joint formation. , 2011, Developmental biology.

[4]  V. Rosen,et al.  Bone morphogenetic protein-9 binds to liver cells and stimulates proliferation. , 1995, Endocrinology.

[5]  V. Agrawal,et al.  Epimorphic regeneration approach to tissue replacement in adult mammals , 2009, Proceedings of the National Academy of Sciences.

[6]  Jangwoo Lee,et al.  SDF-1α/CXCR4 signaling mediates digit tip regeneration promoted by BMP-2. , 2013, Developmental biology.

[7]  T. He,et al.  BMP9 signaling in stem cell differentiation and osteogenesis. , 2018, American journal of stem cells.

[8]  Jangwoo Lee,et al.  Development and Stem Cells Research Article , 2022 .

[9]  J. Dudhia Aggrecan, aging and assembly in articular cartilage , 2005, Cellular and Molecular Life Sciences CMLS.

[10]  Véronique Lefebvre,et al.  The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth. , 2005, The Journal of clinical investigation.

[11]  S. Warming,et al.  Context-dependent signaling defines roles of BMP9 and BMP10 in embryonic and postnatal development , 2013, Proceedings of the National Academy of Sciences.

[12]  Timothy A. Miller,et al.  Nanoparticulate Mineralized Collagen Scaffolds and BMP‐9 Induce a Long‐Term Bone Cartilage Construct in Human Mesenchymal Stem Cells , 2016, Advanced healthcare materials.

[13]  T. He,et al.  BMP9-regulated angiogenic signaling plays an important role in the osteogenic differentiation of mesenchymal progenitor cells , 2013, Journal of Cell Science.

[14]  R. Brentani,et al.  Picrosirius staining plus polarization microscopy, a specific method for collagen detection in tissue sections , 1979, The Histochemical Journal.

[15]  L. David,et al.  Bone Morphogenetic Protein-9 Is a Circulating Vascular Quiescence Factor , 2008, Circulation research.

[16]  Mingquan Yan,et al.  Angiogenesis is inhibitory for mammalian digit regeneration , 2014, Regeneration.

[17]  A. Hess,et al.  Ucma is not necessary for normal development of the mouse skeleton. , 2012, Bone.

[18]  K. Muneoka,et al.  Wound healing and blastema formation in regenerating digit tips of adult mice. , 2011, Developmental biology.

[19]  A. McMahon,et al.  Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. , 1998, Science.

[20]  Jozef Kaiser,et al.  Superficial cells are self‐renewing chondrocyte progenitors, which form the articular cartilage in juvenile mice , 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[21]  H. Ide,et al.  Regeneration potency of mouse limbs , 2007, Development, growth & differentiation.

[22]  S. Ge,et al.  Potential Roles of BMP9 in Liver Fibrosis , 2014, International journal of molecular sciences.

[23]  L. Marrero,et al.  The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse , 2017, Regeneration.

[24]  Zhihao Yao,et al.  Cartilage Tissue Regeneration: The Roles of Cells, Stimulating Factors and Scaffolds. , 2018, Current stem cell research & therapy.

[25]  V. Lefebvre,et al.  Synovial joint morphogenesis requires the chondrogenic action of Sox5 and Sox6 in growth plate and articular cartilage. , 2010, Developmental biology.

[26]  C. Tabin,et al.  BMP2 activity, although dispensable for bone formation, is required for the initiation of fracture healing , 2006, Nature Genetics.

[27]  Connor P. Dolan,et al.  Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine , 2018, Stem cells translational medicine.

[28]  Jangwoo Lee,et al.  BMP2 induces segment-specific skeletal regeneration from digit and limb amputations by establishing a new endochondral ossification center. , 2012, Developmental biology.

[29]  Amitabha Bandyopadhyay,et al.  Genetic Analysis of the Roles of BMP2, BMP4, and BMP7 in Limb Patterning and Skeletogenesis , 2006, PLoS genetics.

[30]  B. Hogan Bone morphogenetic proteins in development. , 1996, Current opinion in genetics & development.

[31]  Sandra J Shefelbine,et al.  BoneJ: Free and extensible bone image analysis in ImageJ. , 2010, Bone.

[32]  L. Marrero,et al.  Expression of doublecortin reveals articular chondrocyte lineage in mouse embryonic limbs , 2011, Genesis.

[33]  Manas Kumar Majumdar,et al.  BMP‐2 and BMP‐9 promotes chondrogenic differentiation of human multipotential mesenchymal cells and overcomes the inhibitory effect of IL‐1 , 2001, Journal of cellular physiology.

[34]  K. Muneoka,et al.  Analogous cellular contribution and healing mechanisms following digit amputation and phalangeal fracture in mice , 2016, Regeneration.

[35]  H. Ide Bone pattern formation in mouse limbs after amputation at the forearm level , 2012, Developmental dynamics : an official publication of the American Association of Anatomists.

[36]  G. Badger,et al.  Early genetic restoration of lubricin expression in transgenic mice mitigates chondrocyte peroxynitrite release and caspase-3 activation. , 2017, Osteoarthritis and cartilage.

[37]  Gretchen L. Humason,et al.  Animal Tissue Techniques , 1974 .

[38]  L. David,et al.  Identification of BMP9 and BMP10 as functional activators of the orphan activin receptor-like kinase 1 (ALK1) in endothelial cells. , 2007, Blood.

[39]  D. Kingsley,et al.  Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes. , 2003, Developmental biology.

[40]  A. Lassar,et al.  Identification of a Prg4‐Expressing Articular Cartilage Progenitor Cell Population in Mice , 2015, Arthritis & rheumatology.

[41]  M. Goumans,et al.  The high affinity ALK1-ligand BMP9 induces a hypertrophy-like state in chondrocytes that is antagonized by TGFβ1. , 2015, Osteoarthritis and cartilage.

[42]  Jangwoo Lee,et al.  Development and regeneration of the neonatal digit tip in mice. , 2008, Developmental biology.

[43]  S. Mundlos,et al.  Mutations in GDF5 Reveal a Key Residue Mediating BMP Inhibition by NOGGIN , 2009, PLoS genetics.

[44]  M. Kjaer,et al.  Radiocarbon dating reveals minimal collagen turnover in both healthy and osteoarthritic human cartilage , 2016, Science Translational Medicine.

[45]  Jin Wang,et al.  Smads, p38 and ERK1/2 are involved in BMP9-induced osteogenic differentiation of C3H10T1/2 mesenchymal stem cells. , 2012, BMB reports.

[46]  V. Lefebvre,et al.  Transcriptional control of chondrocyte specification and differentiation. , 2017, Seminars in cell & developmental biology.

[47]  C. Archer,et al.  Development of synovial joints. , 2003, Birth defects research. Part C, Embryo today : reviews.

[48]  Alan Cheng,et al.  BMP-9 dependent pathways required for the chondrogenic differentiation of pluripotent stem cells. , 2016, Differentiation; research in biological diversity.

[49]  A. Eichmann,et al.  BMP9/ALK1 inhibits neovascularization in mouse models of age-related macular degeneration , 2016, Oncotarget.

[50]  J. Postlethwait,et al.  Ancient origin of lubricated joints in bony vertebrates , 2016, eLife.

[51]  N. Turner,et al.  A histomorphologic study of the normal healing response following digit amputation in C57bl/6 and MRL/MpJ mice. , 2010, Archives of histology and cytology.