Rodríguez-Barrera Roxana, Flores-Romero Adrián, Buzoianu-Anguiano Vinnitsa, Garcia Elisa, Soria-Zavala Karla, Incontri-Abraham Diego, Garibay-López Marcela, Juárez-Vignon Whaley Juan José, Ibarra Antonio
Centro de Investigación en Ciencias de la Salud (CICSA), Facultad de Ciencias de la Salud, Universidad Anáhuac México Campus Norte, Huixquilucan, Mexico.
Proyecto CAMINA A.C., Mexico City, Mexico.
Front Neurol. 2020 Apr 2;11:189. doi: 10.3389/fneur.2020.00189. eCollection 2020.
Immunization with neural derived peptides (INDP), as well as scar removal (SR) and the use of matrices with bone marrow-mesenchymal stem cells (MSCs), have been studied separately and proven to induce a functional and morphological improvement after spinal cord injury (SCI). Herein, we evaluated the therapeutic effects of INDP combined with SR and a fibrin glue matrix (FGM) with MSCs (FGM-MSCs), on motor recovery, axonal regeneration-associated molecules and cytokine expression, axonal regeneration (catecholaminergic and serotonergic fibers), and the induction of neurogenesis after a chronic SCI. For this purpose, female adult rats were subjected to SCI, 60 days after lesion, rats were randomly distributed in four groups: (1) Rats immunized with complete Freund's adjuvant + PBS (vehicle; PBS-I); (2) Rats with SR+ FGM-MSCs; (3) Rats with SR+ INDP + FGM-MSCs; (4) Rats only with INDP. Afterwards, we evaluated motor recovery using the BBB locomotor test. Sixty days after the therapy, protein expression of TNFα, IL-4, IL-10, BDNF, and GAP-43 were evaluated using ELISA assay. The number of catecholaminergic and serotonergic fibers were also determined. Neurogenesis was evaluated through immunofluorescence. The results show that treatment with INDP alone significantly increased motor recovery, anti-inflammatory cytokines, regeneration-associated molecules, axonal regeneration, and neurogenesis when compared to the rest of the groups. Our findings suggest that the combination therapy (SR + INDP + FGM-MSCs) modifies the non-permissive microenvironment post SCI, but it is not capable of inducing an appropriate axonal regeneration or neurogenesis when compared to the treatment with INDP alone.
神经源性肽免疫(INDP)、瘢痕去除(SR)以及使用含骨髓间充质干细胞(MSC)的基质,已分别进行研究,并被证明可在脊髓损伤(SCI)后诱导功能和形态学改善。在此,我们评估了INDP联合SR以及含MSC的纤维蛋白胶基质(FGM-MSC)对慢性SCI后运动恢复、轴突再生相关分子和细胞因子表达、轴突再生(儿茶酚胺能和5-羟色胺能纤维)以及神经发生诱导的治疗效果。为此,对成年雌性大鼠进行SCI,损伤60天后,将大鼠随机分为四组:(1)用完全弗氏佐剂+ PBS免疫的大鼠(载体;PBS-I);(2)接受SR + FGM-MSC治疗的大鼠;(3)接受SR + INDP + FGM-MSC治疗的大鼠;(4)仅接受INDP治疗的大鼠。之后,我们使用BBB运动测试评估运动恢复情况。治疗60天后,使用ELISA测定法评估TNFα、IL-4、IL-10、BDNF和GAP-43的蛋白表达。还测定了儿茶酚胺能和5-羟色胺能纤维的数量。通过免疫荧光评估神经发生情况。结果表明,与其他组相比,单独使用INDP治疗可显著提高运动恢复、抗炎细胞因子、再生相关分子、轴突再生和神经发生。我们的研究结果表明,联合治疗(SR + INDP + FGM-MSC)可改变SCI后的非允许性微环境,但与单独使用INDP治疗相比,它不能诱导适当的轴突再生或神经发生。