Protective effect of astrocyte exosomes on hypoxic-ischemic neurons
HUANG Jing-Lan, QU Yi, TANG Jun, ZOU Rong, LI Shi-Ping, LI Ya-Fei, ZHANG Li, XIA Bin, MU De-Zhi
Department of Pediatrics, West China Second University Hospital/Key Laboratory of Obstetric & Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, Sichuan University, Chengdu 610041, China
Abstract:Objective To study the effect of astrocyte exosomes on hypoxic-ischemic neurons. Methods Rat astrocytes were cultured in vitro, and differential centrifugation was used to obtain the exosomes from the cell supernatant. Transmission electron microscopy, Nanosight, and Western blot were used for the identification of exosomes. BCA method was used to measure the concentration of exosomes. Rat neurons were cultured in vitro and then divided into control group, exosome group, oxygen glucose deprivation (OGD) group, and OGD+exosome group (n=3 each). The OGD and OGD+exosome groups were cultured in glucose-free medium under the hypoxic condition. The exosome and OGD+exosome groups were treated with exosomes at a final concentration of 22 μg/mL. The control and OGD groups were given an equal volume of phosphate-buffered saline. ELISA was used to measure the level of lactate dehydrogenase (LDH) in neurons. The terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling was used to measure the apoptotic index of neurons. Results The identification of exosomes showed that the exosomes extracted by differential centrifugation had the features of exosomes. Compared with the control and exosome groups, the OGD group had significant increases in LDH level and apoptotic index (P < 0.05). Compared with the OGD group, the OGD+exosome group had significant reductions in LDH level and apoptotic index (P < 0.05). Conclusions The exosomes from astrocytes have a protective effect on neurons with hypoxic-ischemic injury.
Shankaran S, Laptook AR, Ehrenkranz RA, et al. Wholebody hypothermia for neonates with hypoxic-ischemic encephalopathy[J]. N Engl J Med, 2005, 353(15):1574-1584.
[2]
Edwards AD, Brocklehurst P, Gunn AJ, et al. Neurological outcomes at 18 months of age after moderate hypothermia for perinatal hypoxic ischaemic encephalopathy:synthesis and meta-analysis of trial data[J]. BMJ, 2010, 340:c363.
[3]
Pappas A, Shankaran S, McDonald SA, et al. Cognitive outcomes after neonatal encephalopathy[J]. Pediatrics, 2015, 135(3):e624-e634.
Verkhratsky A, Matteoli M, Parpura V, et al. Astrocytes as secretory cells of the central nervous system:idiosyncrasies of vesicular secretion[J]. EMBO J, 2016, 35(3):239-257.
[6]
Théry C, Amigorena S, Raposo G, et al. Isolation and characterization of exosomes from cell culture supernatants and biological fluids[J]. Curr Protoc Cell Biol, 2006, 30(1):3.22.1-3.22.29.
[7]
Qu Y, Mao M, Zhao F, et al. Proapoptotic role of human growth and transformation-dependent protein in the developing rat brain after hypoxia-ischemia[J]. Stroke, 2009, 40(8):2843-2848.
[8]
Qu Y, Shi J, Tang Y, et al. MLKL inhibition attenuates hypoxiaischemia induced neuronal damage in developing brain[J]. Exp Neurol, 2016, 279:223-231.
[9]
Zhu J, Qu Y, Lin Z, et al. Loss of PINK1 inhibits apoptosis by upregulating α-synuclein in inflammation-sensitized hypoxicischemic injury in the immature brains[J]. Brain Res, 2016, 1653:14-22.
[10]
Ophelders DR, Wolfs TG, Jellema RK, et al. Mesenchymal stromal cell-derived extracellular vesicles protect the fetal brain after hypoxia-ischemia[J]. Stem Cells Transl Med, 2016, 5(6):754-763.
[11]
Zhang Y, Chopp M, Liu XS, et al. Exosomes derived from mesenchymal stromal cells promote axonal growth of cortical neurons[J]. Mol Neurobiol, 2017, 54(4):2659-2673.
[12]
Li Y, Yang YY, Ren JL, et al. Exosomes secreted by stem cells from human exfoliated deciduous teeth contribute to functional recovery after traumatic brain injury by shifting microglia M1/M2 polarization in rats[J]. Stem Cell Res Ther, 2017, 8(1):198.
[13]
Huang S, Ge X, Yu J, et al. Increased miR-124-3p in microglial exosomes following traumatic brain injury inhibits neuronal inflammation and contributes to neurite outgrowth via their transfer into neurons[J]. FASEB J, 2018, 32(1):512-528.
[14]
Zhang L, Zhang S, Yao J, et al. Microenvironment-induced PTEN loss by exosomal microRNA primes brain metastasis outgrowth[J]. Nature, 2015, 527(7576):100-104.
[15]
Cai S, Shi GS, Cheng HY, et al. Exosomal miR-7 mediates bystander autophagy in lung after focal brain irradiation in mice[J]. Int J Biol Sci, 2017, 13(10):1287-1296.
[16]
Nafar F, Williams JB, Mearow KM. Astrocytes release HspB1 in response to amyloid-β exposure in vitro[J]. J Alzheimers Dis, 2016, 49(1):251-263.