Literature DB >> 33977438

Stem Cell Applications in Lysosomal Storage Disorders: Progress and Ongoing Challenges.

Sevil Köse1, Fatima Aerts-Kaya2,3, Duygu Uçkan Çetinkaya4,2, Petek Korkusuz5.   

Abstract

Lysosomal storage disorders (LSDs) are rare inborn errors of metabolism caused by defects in lysosomal function. These diseases are characterized by accumulation of completely or partially degraded substrates in the lysosomes leading to cellular dysfunction of the affected cells. Currently, enzyme replacement therapies (ERTs), treatments directed at substrate reduction (SRT), and hematopoietic stem cell (HSC) transplantation are the only treatment options for LSDs, and the effects of these treatments depend strongly on the type of LSD and the time of initiation of treatment. However, some of the LSDs still lack a durable and curative treatment. Therefore, a variety of novel treatments for LSD patients has been developed in the past few years. However, despite significant progress, the efficacy of some of these treatments remains limited because these therapies are often initiated after irreversible organ damage has occurred.Here, we provide an overview of the known effects of LSDs on stem cell function, as well as a synopsis of available stem cell-based cell and gene therapies that have been/are being developed for the treatment of LSDs. We discuss the advantages and disadvantages of use of hematopoietic stem cell (HSC), mesenchymal stem cell (MSC), and induced pluripotent stem cell (iPSC)-related (gene) therapies. An overview of current research data indicates that when stem cell and/or gene therapy applications are used in combination with existing therapies such as ERT, SRT, and chaperone therapies, promising results can be achieved, showing that these treatments may result in alleviation of existing symptoms and/or prevention of progression of the disease. All together, these studies offer some insight in LSD stem cell biology and provide a hopeful perspective for the use of stem cells. Further development and improvement of these stem cell (gene) combination therapies may greatly improve the current treatment options and outcomes of patients with a LSD.
© 2021. Springer Nature Switzerland AG.

Entities:  

Keywords:  Gene therapy; Hematopoietic stem cell; Induced pluripotent stem cell; Lysosomal storage disease; Lysosomal storage disorder; Mesenchymal stem cell; Neural stem cell; Stem cell

Mesh:

Year:  2021        PMID: 33977438     DOI: 10.1007/5584_2021_639

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  144 in total

1.  Cord blood is the optimal graft source for the treatment of pediatric patients with lysosomal storage diseases: clinical outcomes and future directions.

Authors:  Mieke Aldenhoven; Joanne Kurtzberg
Journal:  Cytotherapy       Date:  2015-03-31       Impact factor: 5.414

2.  A human neuronal model of Niemann Pick C disease developed from stem cells isolated from patient's skin.

Authors:  Natascha Bergamin; Andrea Dardis; Antonio Beltrami; Daniela Cesselli; Silvia Rigo; Stefania Zampieri; Rossana Domenis; Bruno Bembi; Carlo Alberto Beltrami
Journal:  Orphanet J Rare Dis       Date:  2013-02-21       Impact factor: 4.123

Review 3.  Challenges and opportunities for HSCT outcome registries: perspective from international HSCT registries experts.

Authors:  M Aljurf; J D Rizzo; M Mohty; F Hussain; A Madrigal; M C Pasquini; J Passweg; N Chaudhri; A Ghavamzadeh; H E Solh; Y Atsuta; J Szer; Y Kodera; D Niederweiser; A Gratwohl; M M Horowitz
Journal:  Bone Marrow Transplant       Date:  2014-04-28       Impact factor: 5.483

4.  A New Glucocerebrosidase Chaperone Reduces α-Synuclein and Glycolipid Levels in iPSC-Derived Dopaminergic Neurons from Patients with Gaucher Disease and Parkinsonism.

Authors:  Elma Aflaki; Daniel K Borger; Nima Moaven; Barbara K Stubblefield; Steven A Rogers; Samarjit Patnaik; Frank J Schoenen; Wendy Westbroek; Wei Zheng; Patricia Sullivan; Hideji Fujiwara; Rohini Sidhu; Zayd M Khaliq; Grisel J Lopez; David S Goldstein; Daniel S Ory; Juan Marugan; Ellen Sidransky
Journal:  J Neurosci       Date:  2016-07-13       Impact factor: 6.167

5.  Neuroglial activation in Niemann-Pick Type C mice is suppressed by intracerebral transplantation of bone marrow-derived mesenchymal stem cells.

Authors:  Jae-sung Bae; Shigeki Furuya; So-jeo Ahn; Seong-joon Yi; Yoshio Hirabayashi; Hee Kyung Jin
Journal:  Neurosci Lett       Date:  2005-03-03       Impact factor: 3.046

6.  Bone marrow-derived mesenchymal stem cells promote neuronal networks with functional synaptic transmission after transplantation into mice with neurodegeneration.

Authors:  Jae-Sung Bae; Hyung Soo Han; Dong-Ho Youn; Janet E Carter; Michel Modo; Edward H Schuchman; Hee Kyung Jin
Journal:  Stem Cells       Date:  2007-05       Impact factor: 6.277

7.  Neurodegeneration augments the ability of bone marrow-derived mesenchymal stem cells to fuse with Purkinje neurons in Niemann-Pick type C mice.

Authors:  Jae-Sung Bae; Shigeki Furuya; Yoko Shinoda; Shogo Endo; Edward H Schuchman; Yoshio Hirabayashi; Hee Kyung Jin
Journal:  Hum Gene Ther       Date:  2005-08       Impact factor: 5.695

8.  Neural stem cell implantation extends life in Niemann-Pick C1 mice.

Authors:  Iram Ahmad; Robert E Hunter; Jonathan D Flax; Evan Y Snyder; Robert P Erickson
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

Review 9.  Lysosomal disorders: from storage to cellular damage.

Authors:  Andrea Ballabio; Volkmar Gieselmann
Journal:  Biochim Biophys Acta       Date:  2008-12-08

10.  Enhancing Lysosomal Activation Restores Neural Stem Cell Function During Aging.

Authors:  Amanda J Audesse; Ashley E Webb
Journal:  J Exp Neurosci       Date:  2018-08-23
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