[1] Gordon MK, Hahn RA. Collagens.Cell Tissue Res. 2010;339(1):247-257.[2] Roche P, Czubryt MP. Transcriptional control of collagen I gene expression. Cardiovasc Hematol Disord Drug Targets. 2014;14(2):107-120.[3] Vuorio E, de Crombrugghe B. The family of collagen genes. Annu Rev Biochem. 1990;59:837-872.[4] Jimenez SA, Varga J, Olsen A, et al. Functional analysis of human alpha 1(I) procollagen gene promoter. Differential activity in collagen-producing and -nonproducing cells and response to transforming growth factor beta 1. J Biol Chem. 1994;269(17):12684-12691.[5] Ghosh AK, Yuan W, Mori Y, et al. Antagonistic regulation of type I collagen gene expression by interferon-gamma and transforming growth factor-beta. Integration at the level of p300/CBP transcriptional coactivators. J Biol Chem. 2001; 276(14):11041-11048.[6] Canty EG, Kadler KE. Procollagen trafficking, processing and fibrillogenesis. J Cell Sci. 2005;118(Pt 7):1341-1353.[7] Tasab M, Batten MR, Bulleid NJ. Hsp47: a molecular chaperone that interacts with and stabilizes correctly-folded procollagen. EMBO J. 2000;19(10):2204-2211.[8] Sauk JJ, Norris K, Hebert C, et al. Hsp47 binds to the KDEL receptor and cell surface expression is modulated by cytoplasmic and endosomal pH. Connect Tissue Res. 1998; 37(1-2):105-119.[9] Ishikawa Y, Bächinger HP. A molecular ensemble in the rER for procollagen maturation. Biochim Biophys Acta. 2013;1833 (11):2479-2491.[10] Garnero P. Erratum to: The Role of Collagen Organization on the Properties of Bone. Calcif Tissue Int. 2015;97(3):241.[11] Cohen-Solal L, Zylberberg L, Sangalli A, et al. Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of bone. J Biol Chem. 1994;269(20):14751-14758.[12] Bardai G, Lemyre E, Moffatt P, et al. Osteogenesis Imperfecta Type I Caused by COL1A1 Deletions. Calcif Tissue Int. 2016; 98(1):76-84.[13] Prockop DJ. Mutations that alter the primary structure of type I collagen. The perils of a system for generating large structures by the principle of nucleated growth. J Biol Chem. 1990;265(26):15349-15352.[14] Gerhard DS, Wagner L, Feingold EA, et al. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. 2004; 14(10B):2121-2127.[15] He W, Wu WK, Wu YL, et al. Ginsenoside-Rg1 mediates microenvironment-dependent endothelial differentiation of human mesenchymal stem cells in vitro. J Asian Nat Prod Res. 2011;13(1):1-11.[16] Mizuno M, Fujisawa R, Kuboki Y. Type I collagen-induced osteoblastic differentiation of bone-marrow cells mediated by collagen-alpha2beta1 integrin interaction. J Cell Physiol. 2000; 184(2):207-213.[17] Bortell R, Barone LM, Tassinari MS, et al. Gene expression during endochondral bone development: evidence for coordinate expression of transforming growth factor beta 1 and collagen type I. J Cell Biochem.1990;44(2):81-91.[18] Pittenger MF, Mackay AM, Beck SC, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284(5411):143-147.[19] Aronow MA, Gerstenfeld LC, Owen TA, et al. Factors that promote progressive development of the osteoblast phenotype in cultured fetal rat calvaria cells. J Cell Physiol. 1990;143(2):213-221.[20] Hesse E, Hefferan TE, Tarara JE, et al. Collagen type I hydrogel allows migration, proliferation, and osteogenic differentiation of rat bone marrow stromal cells. J Biomed Mater Res A. 2010;94(2):442-449.[21] Mizuno M, Kuboki Y. Osteoblast-related gene expression of bone marrow cells during the osteoblastic differentiation induced by type I collagen. J Biochem. 2001;129(1):133-138.[22] Linsley C, Wu B, Tawil B. The effect of fibrinogen, collagen type I, and fibronectin on mesenchymal stem cell growth and differentiation into osteoblasts. Tissue Eng Part A. 2013; 19(11-12):1416-1423.[23] Salomon DS. Cell-cell and cell-extracellular matrix adhesion molecules communicate with growth factor receptors: an interactive signaling Web. Cancer Invest. 2000;18(6): 591-593.[24] Staatz WD, Fok KF, Zutter MM, et al. Identification of a tetrapeptide recognition sequence for the alpha 2 beta 1 integrin in collagen. J Biol Chem. 1991;266(12):7363-7367.[25] Puklin-Faucher E, Sheetz MP. The mechanical integrin cycle. J Cell Sci. 2009;122(Pt 2):179-186.[26] Schwartz MA. Integrins, oncogenes, and anchorage independence. J Cell Biol. 1997;139(3):575-578.[27] Wen LP, Fahrni JA, Troie S, et al. Cleavage of focal adhesion kinase by caspases during apoptosis. J Biol Chem. 1997; 272(41):26056-26061.[28] Kim EK, Choi EJ. Pathological roles of MAPK signaling pathways in human diseases. Biochim Biophys Acta. 2010; 1802(4):396-405.[29] Salasznyk RM, Klees RF, Williams WA, et al. Focal adhesion kinase signaling pathways regulate the osteogenic differentiation of human mesenchymal stem cells. Exp Cell Res. 2007;313(1):22-37[30] Jadlowiec J, Koch H, Zhang X, et al. Phosphophoryn regulates the gene expression and differentiation of NIH3T3, MC3T3-E1, and human mesenchymal stem cells via the integrin/MAPK signaling pathway. J Biol Chem. 2004;279(51): 53323-53330. [31] Stein GS, Lian JB, Stein JL, et al. Transcriptional control of osteoblast growth and differentiation. Physiol Rev. 1996;76(2): 593-629.[32] Ganta DR, McCarthy MB, Gronowicz GA. Ascorbic acid alters collagen integrins in bone culture. Endocrinology. 1997;138(9): 3606-3612.[33] 杨志明,屈艺.Ⅰ型胶原—整合素α2β1系统对成骨细胞生物学特性的调控[J].四川大学学报:医学版,2000,31(3):281-284.[34] Wenstrup RJ, Witte DP, Florer JB. Abnormal differentiation in MC3T3-E1 preosteoblasts expressing a dominant-negative type I collagen mutation. Connect Tissue Res.1996;35(1-4): 249-257.[35] Mofid MM, Manson PN, Robertson BC, et al. Craniofacial distraction osteogenesis: a review of 3278 cases. Plast Reconstr Surg. 2001;108(5):1103-1114.[36] Schreuder WH, Jansma J, Bierman MW, et al. Distraction osteogenesis versus bilateral sagittal split osteotomy for advancement of the retrognathic mandible: a review of the literature. Int J Oral Maxillofac Surg. 2007;36(2):103-110.[37] 王大章,陈刚,胡静.牵张成骨在矫治牙颌面畸形中的应用[J].华西口腔医学杂志,1998, 5(4):369-371.[38] Welch RD, Lewis DD. Distraction osteogenesis. Vet Clin North Am Small Anim Pract. 1999,29(5):1187-1205.[39] 柴本甫,汤雪明.实验性骨折愈合的细胞生物学[J].中华骨科杂志, 1991,11(3):203-206.[40] 韦敏,穆雄铮,张涤生,等.颅面牵拉成骨胶原合成的研究[J].口腔颌面外科杂志, 2001, 11(1):32-34.[41] 丁宇翔,刘彦普,敖建华.牙槽突裂牵张成骨胶原合成的研究[J].实用口腔医学杂志, 2005, 21(4):477-479.[42] 商洪涛,刘锐,孙建壮,等.上颌骨缝牵张的组织学变化[J].中国组织工程研究, 2007, 11(10):1833-1836.[43] Chen X, Li N, LeleYang, et al. Expression of collagen I, collagen III and MMP-1 on the tension side of distracted tooth using periodontal ligament distraction osteogenesis in beagle dogs. Arch Oral Biol. 2014;59(11):1217-1225.[44] 姜喜亮,朱晓文,胡静,等.整合素信号通路在大鼠骨髓间充质干细胞牵张中的作用和转导机制[J].中国口腔颌面外科杂志, 2015, 13(3):193-199.[45] Liebschner MA. Biomechanical considerations of animal models used in tissue engineering of bone. Biomaterials. 2004;25(9):1697-1714.[46] Cisneros DA, Hung C, Franz CM, et al. Observing growth steps of collagen self-assembly by time-lapse high-resolution atomic force microscopy. J Struct Biol. 2006;154(3):232-345.[47] Olszta MJ, Cheng X, Sang SJ, et al. Bone structure and formation: A new perspective. Materials Science & Engineering R. 2008; 58 (3) :77-116.[48] Xu Z, Yang Y, Zhao W, et al. Molecular mechanisms for intrafibrillar collagen mineralization in skeletal tissues. Biomaterials. 2015;39:59-66.[49] Wei Z, Huang ZL, Liao SS, et al. Nucleation Sites of Calcium Phosphate Crystals during Collagen Mineralization. Journal of the American Ceramic Society. 2003; 86(6):1052-1054.[50] 涂姜磊,郭富强,吕春春,等.胶原诱导沉积类骨HA及其机制研究[J].生物医学工程学杂志, 2011, 28(1):99-103.[51] Nudelman F, Pieterse K, George A, et al. The role of collagen in bone apatite formation in the presence of hydroxyapatite nucleation inhibitors. Nat Mater. 2010;9(12):1004-1009.[52] Cantaert B, Kim YY, Ludwig H, et al. Think Positive: Phase Separation Enables a Positively Charged Additive to Induce Dramatic Changes in Calcium Carbonate Morphology. Advanced Functional Materials. 2012; 22(5):907-915.[53] Zurick KM, Qin C, Bernards MT. Mineralization induction effects of osteopontin, bone sialoprotein, and dentin phosphoprotein on a biomimetic collagen substrate. J Biomed Mater Res A. 2013;101(6):1571-1581.[54] Qiu ZY, Cui Y, Tao CS, et al. Mineralized Collagen: Rationale, Current Status, and Clinical Applications. Materials (Basel). 2015;8(8):4733-4750.[55] Kerns JG, Buckley K, Churchwell J, et al. Is the Collagen Primed for Mineralization in Specific Regions of the Turkey Tendon? An Investigation of the Protein-Mineral Interface Using Raman Spectroscopy. Anal Chem. 2016;88(3): 1559-1563.[56] Wang Y, Azaïs T, Robin M, et al. The predominant role of collagen in the nucleation, growth, structure and orientation of bone apatite. Nat Mater. 2012;11(8):724-733.[57] Hvistendahl M. China's push in tissue engineering. Science. 2012;338(6109):900-902.[58] Kumar MS, Kirubanandan S, Sripriya R, et al. Triphala incorporated collagen sponge--a smart biomaterial for infected dermal wound healing. J Surg Res. 2010;158(1): 162-170. |