Modulation of the Physical Properties of 3D Spheroids Derived from Human Scleral Stroma Fibroblasts (HSSFs) with Different Axial Lengths Obtained from Surgical Patients

In the current study, to elucidate the pathological characteristics of myopic scleral stroma, three-dimensional (3D) cultures of human scleral stroma fibroblasts (HSSFs) with several axial lengths (AL, 22.80–30.63 mm) that were obtained from patients (n = 7) were examined. Among the three groups of ALs, <25 mm (n = 2), 25–30 mm (n = 2), and >30 mm (n = 3), the physical properties of the 3D HSSFs spheroids with respect to size and stiffness, the expressions of extracellular matrix (ECM) molecules, including collagen (COL) 1, 4, and 6 and fibronectin (FN) by qPCR and immunohistochemistry (IHC), and the mRNA expression of ECM metabolism modulators including hypoxia-inducible factor 1A (HIF 1A), HIF 2A, lysyl oxidase (LOX), tissue inhibitor of metalloproteinase (TIMP) 1–4, and matrix metalloproteinase (MMP) 2, 9, and 14 as well as several endoplasmic reticulum (ER) stress-related factors were compared. In the largest AL group (>30 mm), the 3D HSSFs spheroids were (1) significantly down-sized and less stiff compared to the other groups, and (2) significant changes were detected in the expression of some ECMs (qPCR; the up-regulation of COL1 and COL4, and the down-regulation of FN, IHC; the up-regulation of COL1 and FN, and down-regulation of COL4). The mRNA expressions of ECM modulators and ER stress-related genes were also altered with increasing AL length (up-regulation of HIF2A, MMP2, XBP1, and MMP14, down-regulation of LOX, TIMP 2 and 3, GRP78, GRP94, IRE1, and ATF6). In addition, a substantial down-regulation of some ER stress-related genes (ATF4, sXPB1 and CHOP) was observed in the 25–30 mm AL group. The findings presented herein suggest that small and stiffer 3D HSSFs spheroids in the largest AL group may accurately replicate the pathological significance of scleral thinning and weakening in myopic eyes. In addition, the modulation of several related factors among the different AL groups may also provide significant insights into our understanding of the molecular mechanisms responsible for causing myopic changes in the sclera.

[1]  Yosuke Ida,et al.  Rosiglitasone and ROCK Inhibitors Modulate Fibrogenetic Changes in TGF-β2 Treated Human Conjunctival Fibroblasts (HconF) in Different Manners , 2021, International journal of molecular sciences.

[2]  Yosuke Ida,et al.  Prostaglandin F2α agonists induced enhancement in collagen1 expression is involved in the pathogenesis of the deepening of upper eyelid sulcus , 2021, Scientific Reports.

[3]  Yosuke Ida,et al.  ROCK inhibitors enhance the production of large lipid-enriched 3D organoids of 3T3-L1 cells , 2021, Scientific Reports.

[4]  Yosuke Ida,et al.  ROCK inhibitors beneficially alter the spatial configuration of TGFβ2-treated 3D organoids from a human trabecular meshwork (HTM) , 2020, Scientific Reports.

[5]  J. Qu,et al.  PPARγ modulates refractive development and form deprivation myopia in Guinea pigs. , 2020, Experimental eye research.

[6]  J. Qu,et al.  Crosstalk between EP2 and PPARα Modulates Hypoxic Signaling and Myopia Development in Guinea Pigs , 2020, Investigative ophthalmology & visual science.

[7]  Changqing Zeng,et al.  Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis , 2020, EBioMedicine.

[8]  Yosuke Ida,et al.  Prostaglandin F2α Agonists Negatively Modulate the Size of 3D Organoids from Primary Human Orbital Fibroblasts , 2020, Investigative ophthalmology & visual science.

[9]  Yosuke Ida,et al.  Prostaglandin F2α agonist-induced suppression of 3T3-L1 cell adipogenesis affects spatial formation of extra-cellular matrix , 2020, Scientific Reports.

[10]  Yi Hua,et al.  Scleral structure and biomechanics , 2020, Progress in Retinal and Eye Research.

[11]  Terry J. Smith,et al.  HIF2A–LOX Pathway Promotes Fibrotic Tissue Remodeling in Thyroid-Associated Orbitopathy , 2018, Endocrinology.

[12]  C. Murphy,et al.  Modulation of human corneal stromal cell differentiation by hepatocyte growth factor and substratum compliance , 2018, Experimental eye research.

[13]  Changqing Zeng,et al.  Scleral hypoxia is a target for myopia control , 2018, Proceedings of the National Academy of Sciences.

[14]  N. Mcbrien,et al.  Reduced Scleral TIMP-2 Expression Is Associated With Myopia Development: TIMP-2 Supplementation Stabilizes Scleral Biomarkers of Myopia and Limits Myopia Development. , 2017, Investigative ophthalmology & visual science.

[15]  F. Schaeffel,et al.  Animal models in myopia research , 2015, Clinical & experimental optometry.

[16]  M. Kjaer,et al.  Lysyl Oxidase Activity Is Required for Ordered Collagen Fibrillogenesis by Tendon Cells* , 2015, The Journal of Biological Chemistry.

[17]  Jody A. Summers,et al.  The dynamic sclera: extracellular matrix remodeling in normal ocular growth and myopia development. , 2015, Experimental eye research.

[18]  C. Wildsoet,et al.  Scleral Mechanisms Underlying Ocular Growth and Myopia. , 2015, Progress in molecular biology and translational science.

[19]  G. Semenza,et al.  Adaptive and maladaptive cardiorespiratory responses to continuous and intermittent hypoxia mediated by hypoxia-inducible factors 1 and 2. , 2012, Physiological reviews.

[20]  Terry Kim,et al.  Anatomy and physiology of the cornea , 2011, Journal of cataract and refractive surgery.

[21]  Chia-Yang Liu,et al.  Knockdown of Zebrafish Lumican Gene (zlum) Causes Scleral Thinning and Increased Size of Scleral Coats* , 2010, The Journal of Biological Chemistry.

[22]  B. Ebert,et al.  Failure to prolyl hydroxylate hypoxia‐inducible factor α phenocopies VHL inactivation in vivo , 2006 .

[23]  F. Schaeffel,et al.  Changes in scleral MMP-2, TIMP-2 and TGFbeta-2 mRNA expression after imposed myopic and hyperopic defocus in chickens. , 2006, Experimental eye research.

[24]  J. Rada,et al.  The sclera and myopia. , 2006, Experimental eye research.

[25]  B. Ebert,et al.  Failure to prolyl hydroxylate hypoxia-inducible factor alpha phenocopies VHL inactivation in vivo. , 2006, The EMBO journal.

[26]  T. T. Norton,et al.  Selective regulation of MMP and TIMP mRNA levels in tree shrew sclera during minus lens compensation and recovery. , 2005, Investigative ophthalmology & visual science.

[27]  N. Mcbrien,et al.  Collagen Gene Expression and the Altered Accumulation of Scleral Collagen during the Development of High Myopia* , 2003, The Journal of Biological Chemistry.

[28]  N. Mcbrien,et al.  Role of the sclera in the development and pathological complications of myopia , 2003, Progress in Retinal and Eye Research.

[29]  P. de la Villa,et al.  Refractive changes induced by form deprivation in the mouse eye. , 2003, Investigative ophthalmology & visual science.

[30]  N. Mcbrien,et al.  Structural and ultrastructural changes to the sclera in a mammalian model of high myopia. , 2001, Investigative ophthalmology & visual science.

[31]  N. Mcbrien,et al.  The role of visual information in the control of scleral matrix biology in myopia , 2001, Current eye research.

[32]  N. Mcbrien,et al.  Scleral remodeling during the development of and recovery from axial myopia in the tree shrew. , 2000, Investigative ophthalmology & visual science.

[33]  D. Troilo,et al.  Decreased proteoglycan synthesis associated with form deprivation myopia in mature primate eyes. , 2000, Investigative ophthalmology & visual science.

[34]  A J Adams,et al.  The effect of parental history of myopia on children's eye size. , 1994, JAMA.

[35]  S. Judge,et al.  Ocular development and visual deprivation myopia in the common marmoset (Callithrix jacchus) , 1993, Vision Research.

[36]  F. Keeley,et al.  Characterization of collagen from normal human sclera. , 1984, Experimental eye research.

[37]  D. Goss,et al.  Myopia development in nonhuman primates--a literature review. , 1983, American journal of optometry and physiological optics.

[38]  E S Avetisov,et al.  A study of biochemical and biomechanical qualities of normal and myopic eye sclera in humans of different age groups. , 1983, Metabolic, pediatric, and systemic ophthalmology.

[39]  U. Yinon,et al.  Lid suture myopia in developing chicks: optical and structural considerations. , 1982, Current eye research.

[40]  D. Goss,et al.  Myopia Development in Experimental Animals—A Literature Review , 1981, American journal of optometry and physiological optics.

[41]  T. Wiesel,et al.  Myopia and eye enlargement after neonatal lid fusion in monkeys , 1977, Nature.

[42]  B. Curtin The posterior staphyloma of pathologic myopia. , 1977, Transactions of the American Ophthalmological Society.

[43]  JON S. LARSEN,et al.  THE SAGITTAL GROWTH OF THE EYE , 1971, Acta ophthalmologica.