scholarly journals Cord blood cell-derived iPSCs as a new candidate for chondrogenic differentiation and cartilage regeneration

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Yoojun Nam ◽  
Yeri Alice Rim ◽  
Seung Min Jung ◽  
Ji Hyeon Ju
2006 ◽  
Vol 12 (6) ◽  
pp. 1651-1661 ◽  
Author(s):  
Seung-Woo Cho ◽  
So-Jung Gwak ◽  
Sun-Woong Kang ◽  
Suk Ho Bhang ◽  
Kang Won Song ◽  
...  

Life ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1007
Author(s):  
Alisa A. Shaimardanova ◽  
Daria S. Chulpanova ◽  
Valeriya V. Solovyeva ◽  
Ekaterina E. Garanina ◽  
Ilnur I. Salafutdinov ◽  
...  

Tay-Sachs disease (TSD) is a progressive neurodegenerative disorder that occurs due to a deficiency of a β hexosaminidase A (HexA) enzyme, resulting in the accumulation of GM2 gangliosides. In this work, we analyzed the effect of umbilical cord blood cell transplantation (UCBCT) and curcumin administration on the course of the disease in a patient with adult TSD. The patient’s serum cytokine profile was determined using multiplex analysis. The level of GM2 gangliosides in plasma was determined using mass spectrometry. The enzymatic activity of HexA in the plasma of the patient was assessed using a fluorescent substrate assay. The HexA α-subunit (HexA) concentration was determined using ELISA. It was shown that both UCBCT and curcumin administration led to a change in the patient’s cytokine profile. The UCBCT resulted in an increase in the concentration of HexA in the patient’s serum and in an improvement in the patient’s neurological status. However, neither UCBCT nor curcumin were able to alter HexA activity and the level of GM2 in patient’s plasma. The data obtained indicate that UCBCT and curcumin administration can alter the immunity of a patient with TSD, reduce the level of inflammatory cytokines and thereby improve the patient’s condition.


Neuroreport ◽  
2009 ◽  
Vol 20 (4) ◽  
pp. 354-359 ◽  
Author(s):  
Hong-Tian Zhang ◽  
Hao-Yu Cheng ◽  
Liang Zhang ◽  
Juan Fan ◽  
Yi-Zhao Chen ◽  
...  

2019 ◽  
Vol 28 (9-10) ◽  
pp. 1329-1332 ◽  
Author(s):  
Paul R. Sanberg ◽  
Jared Ehrhart

The therapeutic application of human umbilical cord blood cells has been an area of great interest for at least the last 25 years. Currently, cord blood cells are approved for reconstitution of the bone marrow following myeloablation in both young and old patients with myeloid malignancies and other blood cancers. Translational studies investigating alternative uses of cord blood have also shown that these cells not only stimulate neurogenesis in the aged brain but are also potentially therapeutic in the treatment of adult neurodegenerative disorders including amyotrophic lateral sclerosis, Alzheimer’s disease, ischemic stroke, traumatic brain injury, and Parkinson’s disease. Recent advances in the clinical application of cord blood cells by Dr. Joanne Kurtzberg and colleagues have found that non-HLA matched allogeneic banked cord blood units in immunocompetent patients with ischemic stroke are safe and well tolerated. Although the exact mechanism(s) of action that provide the beneficial effects observed from a cord blood cell-based therapy are currently unknown, several studies using models of neurodegenerative disease have shown these cells are immune-modulatory and anti-inflammatory. Thus, any future clinical studies investigating the efficacy of this cord blood cell therapeutic would strongly benefit from the inclusion of methodologies to determine changes in both markers of inflammation and the response of immune tissues, such as the spleen, in subjects receiving cell infusion.


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