Induction of Differentiation of Mesenchymal Stem Cells into Retinal Pigment Epithelial Cells for Retinal Regeneration by Using Ciliary Neurotrophic Factor in Diabetic Rats

Qing Huang , Yi Ding , Ji-guo Yu , Jing Li , Yi Xiang , Na Tao

Current Medical Science ›› 2021, Vol. 41 ›› Issue (1) : 145 -152.

PDF
Current Medical Science ›› 2021, Vol. 41 ›› Issue (1) : 145 -152. DOI: 10.1007/s11596-021-2329-y
Article

Induction of Differentiation of Mesenchymal Stem Cells into Retinal Pigment Epithelial Cells for Retinal Regeneration by Using Ciliary Neurotrophic Factor in Diabetic Rats

Author information +
History +
PDF

Abstract

Diabetic retinopathy (DR) is a common cause of blindness all over the world. Bone marrow mesenchymal stem cells (BMSCs) have been considered as a promising strategy for retinal regeneration in the treatment of DR. However, the poor viability and low levels of BMSCs engraftment limit the therapeutic potential of BMSCs. The present study aimed to examine the direct induction of BMSCs differentiation into the cell types related to retinal regeneration by using soluble cytokine ciliary neurotrophic factor (CNTF). We observed remarkably increased expression of cellular retinaldehyde-binding protein (CRALBP) and retinoid isomerohydrolase (RPE65) in BMSCs treated with CNTF in vitro, indicating the directional differentiation of BMSCs into the retinal pigment epithelium (RPE) cells, which are crucial for retinal healing. In vivo, the diabetic rat model was established by use of streptozotocin (STZ), and animals treated with BMSCs+CNTF exhibited better viability and higher delivery efficiency of the transplanted cells than those treated with BMSCs injection alone. Similar to the in-vitro result, treatment with BMSCs and CNTF combined led to the differentiation of BMSCs into beneficial cells (RPE cells), and accelerated retinal healing characterized by the activation of rod photoreceptor cells and phagocytosis function of RPE cells. In conclusion, CNTF contributes to the differentiation of BMSCs into RPE cells, which may help overcome the current stem cell therapy limitations in the field of retinal regeneration.

Keywords

mesenchymal stem cells / differentiation / ciliary neurotrophic factor / retinal regeneration / retinal pigment epithelium (RPE)

Cite this article

Download citation ▾
Qing Huang, Yi Ding, Ji-guo Yu, Jing Li, Yi Xiang, Na Tao. Induction of Differentiation of Mesenchymal Stem Cells into Retinal Pigment Epithelial Cells for Retinal Regeneration by Using Ciliary Neurotrophic Factor in Diabetic Rats. Current Medical Science, 2021, 41(1): 145-152 DOI:10.1007/s11596-021-2329-y

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

StraussO. The retinal pigment epithelium in visual function. Physiol Rev, 2005, 85(3): 845-881

[2]

Marchese C, Felici A, Visco V, et al. Fibroblast growth factor 10 induces proliferation and differentiation of human primary cultured keratinocytes. J Invest Dermatol, 2001(116):623–628

[3]

DiCiccoRM, BellBA, KaulC, et al.. Retinal regeneration following OCT-guided laser injury in zebrafish. Invest Ophthalmol Vis Sci, 2014, 55(10): 6281-6288

[4]

RamsdenCM, PownerMB, CarrAJ, et al.. Stem cells in retinal regeneration: past, present and future. Development, 2013, 140(12): 2576-2585

[5]

RajashekharG. Mesenchymal stem cells: new players in retinopathy therapy. Front Endocrinol, 2014, 5: 59

[6]

RajashekharG, RamadanA, AbburiC, et al.. Regenerative therapeutic potential of adipose stromal cells in early stage diabetic retinopathy. PloS one, 2014, 9(1): e84671

[7]

YangZ, LiK, YanX, et al.. Amelioration of diabetic retinopathy by engrafted human adipose-derived mesenchymal stem cells in streptozotocin diabetic rats. Graefes Arch Clin Exp Ophthalmol, 2010, 248(10): 1415-1422

[8]

KlassenHJ, NgTF, KurimotoY, et al.. Multipotent retinal progenitors express developmental markers, differentiate into retinal neurons, and preserve lightmediated behavior. Invest Ophthalmol Vis Sci, 2004, 45(11): 4167-4173

[9]

PearsonRA, BarberAC, RizziM, et al.. Restoration of vision after transplantation of photoreceptors. Nature, 2012, 485(7396): 99-103

[10]

ZhangY, WangW. Effects of bone marrow mesenchymal stem cell transplantation on light-damaged retina. Invest Ophthalmol Vis Sci, 2010, 51(7): 3742-3748

[11]

Goldenberg-CohenN, Avraham-LubinBC, SadikovT, et al.. Effect of coadministration of neuronal growth factors on neuroglial differentiation of bone marrow-derived stem cells in the ischemic retina. Invest Ophthalmol Vis Sci, 2014, 55(1): 502-512

[12]

Cislo-PakulukA, MaryczK. A Promising Tool in Retina Regeneration: Current Perspectives and Challenges When Using Mesenchymal Progenitor Stem Cells in Veterinary and Human Ophthalmological Applications. Stem cell Rev Rep, 2017, 13(5): 598-602

[13]

ChoiSW, KimJJ, SeoMS, et al.. Inhibition by miR-410 facilitates direct retinal pigment epithelium differentiation of umbilical cord blood-derived mesenchymal stem cells. J Vet Sci, 2017, 18(1): 59-65

[14]

BullND, IrvineKA, FranklinRJ, et al.. Transplanted oligodendrocyte precursor cells reduce neurodegeneration in a model of glaucoma. Invest Ophthalmol Vis Sci, 2009, 50(9): 4244-4253

[15]

XiaJ, LuoM, NiN, et al.. Bone marrow mesenchymal stem cells stimulate proliferation and neuronal differentiation of retinal progenitor cells. PloS one, 2013, 8(9): e76157

[16]

AkbarzadehA, NorouzianD, MehrabiM, et al.. Induction of diabetes by streptozotocin in rats. Indian J Clin Biochem, 2007, 22(2): 60-64

[17]

CarvalhoAB, QuintanilhaLF, DiasJV, et al.. Bone marrow multipotent mesenchymal stromal cells do not reduce fibrosis or improve function in a rat model of severe chronic liver injury. Stem Cells, 2008, 26(5): 1307-1314

[18]

HouC, ShenL, HuangQ, et al.. The effect of heme oxygenase-1 complexed with collagen on MSC performance in the treatment of diabetic ischemic ulcer. Biomaterials, 2013, 34(1): 112-120

[19]

InoueY, IriyamaA, UenoS, et al.. Subretinal transplantation of bone marrow mesenchymal stem cells delays retinal degeneration in the RCS rat model of retinal degeneration. Exp Eye Res, 2007, 85(2): 234-241

[20]

HuntNC, HallamD, KarimiA, et al.. 3D culture of human pluripotent stem cells in RGD-alginate hydrogel improves retinal tissue development. Acta Biomater, 2017, 49: 329-343

[21]

KuttyRK, SamuelW, BoyceK, et al.. Proinflammatory cytokines decrease the expression of genes critical for RPE function. Mol Vis, 2016, 22: 1156-1168

[22]

EzquerM, UrzuaCA, MontecinoS, et al.. Intravitreal administration of multipotent mesenchymal stromal cells triggers a cytoprotective microenvironment in the retina of diabetic mice. Stem Cell Res Ther, 2016, 7: 42

[23]

JohnsonTV, BullND, MartinKR. Identification of barriers to retinal engraftment of transplanted stem cells. Invest Ophthalmol Vis Sci, 2010, 51(2): 960-970

[24]

AdlerR, LandaKB, ManthorpeM, et al.. Cholinergic neuronotrophic factors: intraocular distribution of trophic activity for ciliary neurons. Science, 1979, 204(4400): 1434-1436

[25]

BeltranWA, ZhangQ, KijasJW, et al.. Cloning, mapping, and retinal expression of the canine ciliary neurotrophic factor receptor alpha (CNTFRalpha). Invest Ophthalmol Vis Sci, 2003, 44(8): 3642-3649

[26]

LiR, WenR, BanzonT, et al.. CNTF mediates neurotrophic factor secretion and fluid absorption in human retinal pigment epithelium. PloS One, 2001, 6(9): e23148

[27]

AizuY, KatayamaH, TakahamaS, et al.. Topical instillation of ciliary neurotrophic factor inhibits retinal degeneration in streptozotocin-induced diabetic rats. Neuroreport, 2003, 14(16): 2067-2071

[28]

BrayAF, CevallosRR, GazarianK, et al.. Human dental pulp stem cells respond to cues from the rat retina and differentiate to express the retinal neuronal marker rhodopsin. Neuroscience, 2014, 280: 142-155

[29]

HuangZ, HuZ, XieP, et al.. Tyrosine-mutated AAV2-mediated shRNA silencing of PTEN promotes axon regeneration of adult optic nerve. PloS One, 2017, 12(3): e0174096

AI Summary AI Mindmap
PDF

88

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/