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        水凝支架三維培養(yǎng)系統(tǒng),水凝膠基質(zhì)力學(xué)環(huán)境模擬系統(tǒng),水凝膠基質(zhì)力學(xué)環(huán)境系統(tǒng),生物材料細(xì)胞力學(xué)微環(huán)境體外構(gòu)建系統(tǒng)

        型號(hào):fx-5000tt
        聯(lián)系人:李勝亮
        聯(lián)系電話:18618101725
        品牌:美國(guó)flexercell

        三維種子細(xì)胞構(gòu)建人工生物組織系統(tǒng)(Creating a Bioartifical Construct with the Tissue Train System)

        特點(diǎn):

        1)對(duì)生長(zhǎng)在三維狀態(tài)下的細(xì)胞進(jìn)行靜態(tài)的或者周期性的牽張拉伸刺激培養(yǎng),可以進(jìn)行實(shí)時(shí)觀察分析。

        2)對(duì)生長(zhǎng)在三維環(huán)境下的細(xì)胞進(jìn)行單軸向或者雙軸向的靜態(tài)或者周期性的應(yīng)力加載實(shí)驗(yàn)

        3)可建立te制的各種模擬實(shí)驗(yàn):心率模擬實(shí)驗(yàn),步行模擬實(shí)驗(yàn),跑動(dòng)模擬實(shí)驗(yàn)和其他動(dòng)力模擬實(shí)驗(yàn)。
        4)構(gòu)建長(zhǎng)度達(dá)35mm的生物人工組織

        5)具有豐富的三維培養(yǎng)模具和多種蛋白包被材料的自動(dòng)細(xì)胞組織三維培養(yǎng)系統(tǒng)




        6)該系統(tǒng)以立體水凝膠為三維培養(yǎng)支架, 水凝膠支架具有大量體內(nèi)微環(huán)境基質(zhì)的特征,水凝膠所具有的三維網(wǎng)絡(luò)結(jié)構(gòu)、含水量高和力學(xué)性能可控等特性與體內(nèi)細(xì)胞所處基質(zhì)微環(huán)境相似, 被廣泛用于工程化組織的體外構(gòu)建研究,水凝膠的硬度調(diào)控范圍很大, 非常有利于模擬體內(nèi)生理或病理力學(xué)微環(huán)境
        是真正意義上的三維培養(yǎng)系統(tǒng)




        7)配套的scanflex掃描分析模塊可以記錄三維人工組織中凝膠的壓實(shí)過(guò)程、記錄三維細(xì)胞培養(yǎng)凝膠的壓實(shí)動(dòng)力學(xué)、凝膠面積計(jì)算

        An automated scanning device with area measurement software.

        • Measure gel compaction in 3D bioartificial tissues.
        • Scans and saves images up to 600 dpi of 3D tissue constructs.
        • Can be used in conjunction with the Tissue Train® Culture System.
        Read more about Tissue Engineering with flexercell® products.

        適用范圍

        1)flexercell的Tissue Train ®培養(yǎng)體系,是為了解決這一組織培養(yǎng)過(guò)程中的難題,這個(gè)培養(yǎng)體系通過(guò)為細(xì)胞和基質(zhì)提供三維支架矩陣組織、動(dòng)態(tài)的拉伸力和多種幾何模型來(lái)創(chuàng)建不同形狀的生物人工組織(如線性,梯形和圓形)。


        2水凝膠基質(zhì)力學(xué)環(huán)境模擬

        3)生物材料的細(xì)胞力學(xué)微環(huán)境體外構(gòu)建系統(tǒng)

        4)基于干細(xì)胞3D力學(xué)環(huán)境的工程化微組織構(gòu)建研究



        Tissue Train® Bioartificial Tissue Fabrication with Uniaxial Strain

        A 3D collagen cell-seeded construct (or bioartifical tissue) is dispensed with a pipette into a linear mold created with the  Trough Loader® and Tissue Train® System. After the construct has polymerized, the flexercell® Tension System can be used with an Arctangle® Loading Station? to apply uniaxial strain to the construct.

        Tension Test of a Bioartificial Tissue
        A 3D cell-seeded collagen gel created with the Tissue Train® System is subjected to a tensile test until failure. Shown here is the construct within the test grips during testing

        Tissue Train® Trapezoidal Construct under Tension with Corresponding Finite Element Strain Values
        Trapezoidal-shaped 3D cell-seeded gel construct (created with the flexercell® Tissue Train®System) undergoing unconstrained tension applied with the FX-5000? Tension System. The strain values, as determined with Finite Element Analysis, are depicted alongside the strained construct.

        Tissue Train ®培養(yǎng)系統(tǒng)應(yīng)用背景

        體外培養(yǎng)在與真實(shí)組織在結(jié)構(gòu)上和功能上相似的人工組織需要以下幾個(gè)基本條件:

        (1)細(xì)胞

        (2)支架矩陣組織

        (3)培養(yǎng)基和生長(zhǎng)因子和(4)機(jī)械刺激。這些條件彼此相互影響,并且相互之間共同來(lái)促進(jìn)形成能夠承受生物機(jī)械力的,且結(jié)構(gòu)比較穩(wěn)定的組織。而在人工組成形成的過(guò)程中,這些細(xì)胞按照發(fā)育途徑形成具有一定幾何形狀的細(xì)胞外基質(zhì)結(jié)構(gòu)。其中一些信號(hào)轉(zhuǎn)導(dǎo)途徑參與了細(xì)胞外基質(zhì)組合物的形成。這些途徑中,有些是由細(xì)胞基質(zhì)的機(jī)械變形調(diào)節(jié),并通過(guò)膜結(jié)合蛋白,如整合素,粘著斑復(fù)合體,細(xì)胞粘附分子和離子通道傳遞到細(xì)胞內(nèi)。這些途徑中細(xì)胞還可以響應(yīng)配體,如細(xì)胞基質(zhì)形變所釋放的細(xì)胞因子,激素或生長(zhǎng)因子等。

        為了維持肌肉骨骼組織的完整性和強(qiáng)度,組織內(nèi)細(xì)胞需要保持一定水平的的內(nèi)在應(yīng)力。如果缺乏這種內(nèi)在的應(yīng)力,組織會(huì)缺少?gòu)?qiáng)度導(dǎo)致細(xì)胞結(jié)構(gòu)的破壞或者組織的斷裂。目前一般認(rèn)為如果在固定四肢,臥床休息或在內(nèi)在應(yīng)力水平的降低的情況下,將導(dǎo)致骨中礦物質(zhì)流失,骨組織萎縮,骨骼弱化,以及合成代謝活性的降低和分解代謝活性的增加。

        為了在體外培養(yǎng)與原生組織類似的人工組織,重要的就是能夠創(chuàng)建模擬體內(nèi)條件的環(huán)境。細(xì)胞在具有機(jī)械運(yùn)動(dòng)作用的的環(huán)境中培養(yǎng),可以促進(jìn)細(xì)胞的新陳代謝,并可以改變細(xì)胞的形狀和其它性能。因此,在體外形成過(guò)程中建立和保持一個(gè)具備機(jī)械作用的環(huán)境(即張力,剪切力或壓縮)就成為這一過(guò)程中至關(guān)重要的。除了具備機(jī)械作用的環(huán)境,在三維環(huán)境下培養(yǎng)細(xì)胞可以比靜態(tài)二維培養(yǎng)法更好地模擬原生環(huán)境。






        典型應(yīng)用文獻(xiàn)摘選:

         

        1. Abraham T, Kayra D, McManus B, Scott A. Quantitative assessment of forward and backward second harmonic three dimensional images of collagen type I matrix remodeling in a stimulated cellular environment. J Struct Biol 180(1):17-25, 2012.

        2. Ahearne M, Bagnaninchi PO, Yang Y, El Haj AJ. Online monitoring of collagen fibre alignment in tissue-engineered tendon by PSOCT. J Tissue Eng Regen Med 2(8):521-524, 2008.

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        5. Bertrand AT, Ziaei S, Ehret C, Duchemin H, Mamchaoui K, Bigot A, Mayer M, Quijano-Roy S, Desguerre I, Lainé J, Ben Yaou R, Bonne G, Coirault C. Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors. J Cell Sci 127(Pt 13):2873-84, 2014.

        6. Cao TV, Hicks MR, Campbell D, Standley PR. Dosed myofascial release in three-dimensional bioengineered tendons: effects on human fibroblast hyperplasia, hypertrophy, and cytokine secretion. J Manipulative Physiol Ther 36(8):513-21, 2013.

        7. Cao TV, Hicks MR, Zein-Hammoud M, Standley PR. Duration and magnitude of myofascial release in 3-dimensional bioengineered tendons: effects on wound healing. J Am Osteopath Assoc 115(2):72-82, 2015.

        8. Charoenpanich A, Wall ME, Tucker CJ, Andrews DM, Lalush DS, Loboa EG. Microarray analysis of human adipose-derived stem cells in three-dimensional collagen culture: osteogenesis inhibits bone morphogenic protein and Wnt signaling pathways, and cyclic tensile strain causes upregulation of proinflammatory cytokine regulators and angiogenic factors. Tissue Eng Part A 17(21-22):2615-2627, 2011.

        9. Clause KC, Tinney JP, Liu LJ, Gharaibeh B, Huard J, Kirk JA, Shroff SG, Fujimoto KL, Wagner WR, Ralphe JC, Keller BB, Tobita K. A three-dimensional gel bioreactor for assessment of cardiomyocyte induction in letal muscle-derived stem cells. Tissue Eng Part C Methods 16(3):375-385, 2010.

        10. Clause KC, Tinney JP, Liu LJ, Keller BB, Tobita K. Engineered early embryonic cardiac tissue increases cardiomyocyte proliferation by cyclic mechanical stretch via p38-MAP kinase phosphorylation. Tissue Engineering Part A 15(6):1373-1380, 2009.

        11. Clause KC, Tinney JP, Liu JL, Keller BB, Huard J, Tobita K. p38MAP-kinase regulates cardiomyocyte proliferation and contractile properties of engineered early embryonic cardiac tissue [abstract]. Weinstein Cardiovascular Development Research Conference, Indianapolis, IN, 2007.

        12. Clause KC, Tinney JP, Liu JL, Gharaibeh B, Fujimoto LK, Wagner WR, Ralphe JC, Keller BB, Huard J, Tobita K. Functioning engineered cardiac tissue from letal muscle derived stem cells [abstract]. 4th Annual Symposium of AHA Council on Basic Cardiovascular Sciences, Keystone CO, 2007.

        13. de Jonge N, Foolen J, Brugmans MC, S?ntjens SH, Baaijens FP, Bouten CV. Degree of scaffold degradation influences collagen (re)orientation in engineered tissues. Tissue Eng Part A 20(11-12):1747-57, 2014.

        14. de Lange WJ, Grimes AC, Hegge LF, Ralphe JC. Ablation of cardiac myosin-binding protein-C accelerates contractile kinetics in engineered cardiac tissue. J Gen Physiol 141(1):73-84, 2013.

        15. Ferdous Z, Lazaro LD, Iozzo RV, H??k M, Grande-Allen KJ. Influence of cyclic strain and decorin deficiency on 3D cellularized collagen matrices. Biomaterials 29(18):2740-2748, 2008.

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        18. Henshaw DR, Attia E, Bhargava M, Hannafin JA. Canine ACL fibroblast integrin expression and cell alignment in response to cyclic tensile strain in three-dimensional collagen gels. J Orthop Res 24(3):481-490, 2006.

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        21. Jones ER, Jones GC, Legerlotz K, Riley GP. Cyclical strain modulates metalloprotease and matrix gene expression in human tenocytes via activation of TGFβ. Biochim Biophys Acta 1833(12):2596-2607, 2013.

        22. Lee CH, Shin HJ, Cho IH, Kang YM, Kim IA, Park KD, Shin JW. Nanofiber alignment and direction of mechanical strain affect the ECM production of human ACL fibroblast. Biomaterials 26(11):1261-1270, 2005.

        23. Masumoto H, Nakane T, Tinney JP, Yuan F, Ye F, Kowalski WJ, Minakata K, Sakata R, Yamashita JK, Keller BB. The myocardial regenerative potential of three-dimensional engineered cardiac tissues composed of multiple human iPS cell-derived cardiovascular cell lineages. Sci Rep 6:29933, 2016.

        24. Nguyen MD, Tinney JP, Ye F, Elnakib AA, Yuan F, El-Baz A, Sethu P, Keller BB, Giridharan GA. Effects of physiologic mechanical stimulation on embryonic chick cardiomyocytes using a microfluidic cardiac cell culture model. Anal Chem 87(4):2107-13, 2015.

        25. Nieponice A, Maul TM, Cumer JM, Soletti L, Vorp DA. Mechanical stimulation induces morphological and phenotypic changes in bone marrow-derived progenitor cells within a three-dimensional fibrin matrix. J Biomed Mater Res A 81(3):523-530, 2007.

        26. Nourse MB, Halpin DE, Scatena M, Mortisen DJ, Tulloch NL, Hauch KD, Torok-Storb B, Ratner BD, Pabon L, Murry CE. VEGF induces differentiation of functional endothelium from human embryonic stem cells: implications for tissue engineering. Arterioscler Thromb Vasc Biol 30(1):80-89, 2010.

        27. Peters AS, Brunner G, Krieg T, Eckes B. Cyclic mechanical strain induces TGFβ1-signalling in dermal fibroblasts embedded in a 3D collagen lattice. Arch Dermatol Res 307(2):191-7, 2015.

         

         

        28. Qi J, Chi L, Bynum D, Banes AJ. Gap junctions in IL-1β-mediated cell survival response to strain. J Appl Physiol 110(5):1425-1431, 2011.

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