Expansion, characterisation and differentiation of human neural stem cells
Stroke irreversibly damages affected brain part, leading to permanent neuronal impairment. Neural stem cell (NSC)-based therapy is a potential stroke treatment due to its ability to self-renew and to differentiate into various viable neuronal cells for damaged brain tissue regeneration. Here, huma...
| Main Author: | |
|---|---|
| Format: | Monograph |
| Language: | English |
| Published: |
Universiti Sains Malaysia
2015
|
| Subjects: | |
| Online Access: | http://eprints.usm.my/60657/1/YEE%20MAY%20YE%20-%20e.pdf |
| _version_ | 1825908323771219968 |
|---|---|
| author | Ye, Yee May |
| author_facet | Ye, Yee May |
| author_sort | Ye, Yee May |
| collection | USM |
| description | Stroke irreversibly damages affected brain part, leading to permanent neuronal
impairment. Neural stem cell (NSC)-based therapy is a potential stroke treatment due to
its ability to self-renew and to differentiate into various viable neuronal cells for damaged brain tissue regeneration. Here, human NSCs were expanded from GIBCO® human NSC line and stroke patients’ brain subventricular zone (SVZ) tissue biopsy
with ethical approval. NSCs obtained from GIBCO® cell line were used for pilot testing of NSC characterisation and differentiation ability in vitro. GIBCO® NSCs were cultured in complete StemPro®NSC SFM while human brain SVZ tissues were cultured in an adherent layer with serum-free medium containing bFGF and EGF.
Characterisation of NSC was performed using qRT-PCR and Western blot; while NSC
differentiation was performed using Neuron Differentiation Medium and Astrocytes
Differentiation Medium. Both assays used human normal brain cell line (SVG-pl2) as
negative control. qRT-PCR data illustrated that NSCs showed over 4000-fold difference
in Nestin and 6000-fold difference in CD133 expression compared to SVG-pl2,
indicated that Nestin and CD 133 were specific to NSC. These results were consistent
with the Western blot data in which Nestin protein with approximately 200 kDa was
identified in NSCs but was absent in SVG-pl2. Upon four days in culture with
differentiation media, NSCs did not show morphological changes towards neurons and
astrocytes respectively, compared to non-treated cells. This is due to the limited time
available to perform this assay in present study. Longer culture duration which is more
than one week will be performed in future to obtain more accurate result. Meanwhile,
two clonal neurospheres were obtained from SVZ tissue culture, indicated that the culture method used in this study was successful to isolate NSCs. However,
neurosphere contains only small amount of true stem cells, thus cell disaggregation and
proliferation are suggested in future study to obtain more cells for downstream analysis.
Conclusion, NSCs were successfully obtained from both GIBCO® human NSC line and
SVZ tissue. However, further expansion, characterisation and differentiation of NSC
isolated from SVZ tissue should be performed in future study. |
| first_indexed | 2024-09-25T03:56:52Z |
| format | Monograph |
| id | usm.eprints-60657 |
| institution | Universiti Sains Malaysia |
| language | English |
| last_indexed | 2024-09-25T03:56:52Z |
| publishDate | 2015 |
| publisher | Universiti Sains Malaysia |
| record_format | dspace |
| spelling | usm.eprints-606572024-05-29T08:12:52Z http://eprints.usm.my/60657/ Expansion, characterisation and differentiation of human neural stem cells Ye, Yee May R Medicine (General) RA440-440.87 Study and teaching. Research Stroke irreversibly damages affected brain part, leading to permanent neuronal impairment. Neural stem cell (NSC)-based therapy is a potential stroke treatment due to its ability to self-renew and to differentiate into various viable neuronal cells for damaged brain tissue regeneration. Here, human NSCs were expanded from GIBCO® human NSC line and stroke patients’ brain subventricular zone (SVZ) tissue biopsy with ethical approval. NSCs obtained from GIBCO® cell line were used for pilot testing of NSC characterisation and differentiation ability in vitro. GIBCO® NSCs were cultured in complete StemPro®NSC SFM while human brain SVZ tissues were cultured in an adherent layer with serum-free medium containing bFGF and EGF. Characterisation of NSC was performed using qRT-PCR and Western blot; while NSC differentiation was performed using Neuron Differentiation Medium and Astrocytes Differentiation Medium. Both assays used human normal brain cell line (SVG-pl2) as negative control. qRT-PCR data illustrated that NSCs showed over 4000-fold difference in Nestin and 6000-fold difference in CD133 expression compared to SVG-pl2, indicated that Nestin and CD 133 were specific to NSC. These results were consistent with the Western blot data in which Nestin protein with approximately 200 kDa was identified in NSCs but was absent in SVG-pl2. Upon four days in culture with differentiation media, NSCs did not show morphological changes towards neurons and astrocytes respectively, compared to non-treated cells. This is due to the limited time available to perform this assay in present study. Longer culture duration which is more than one week will be performed in future to obtain more accurate result. Meanwhile, two clonal neurospheres were obtained from SVZ tissue culture, indicated that the culture method used in this study was successful to isolate NSCs. However, neurosphere contains only small amount of true stem cells, thus cell disaggregation and proliferation are suggested in future study to obtain more cells for downstream analysis. Conclusion, NSCs were successfully obtained from both GIBCO® human NSC line and SVZ tissue. However, further expansion, characterisation and differentiation of NSC isolated from SVZ tissue should be performed in future study. Universiti Sains Malaysia 2015 Monograph NonPeerReviewed application/pdf en http://eprints.usm.my/60657/1/YEE%20MAY%20YE%20-%20e.pdf Ye, Yee May (2015) Expansion, characterisation and differentiation of human neural stem cells. Project Report. Universiti Sains Malaysia. |
| spellingShingle | R Medicine (General) RA440-440.87 Study and teaching. Research Ye, Yee May Expansion, characterisation and differentiation of human neural stem cells |
| title | Expansion, characterisation and
differentiation of human neural stem
cells |
| title_full | Expansion, characterisation and
differentiation of human neural stem
cells |
| title_fullStr | Expansion, characterisation and
differentiation of human neural stem
cells |
| title_full_unstemmed | Expansion, characterisation and
differentiation of human neural stem
cells |
| title_short | Expansion, characterisation and
differentiation of human neural stem
cells |
| title_sort | expansion characterisation and differentiation of human neural stem cells |
| topic | R Medicine (General) RA440-440.87 Study and teaching. Research |
| url | http://eprints.usm.my/60657/1/YEE%20MAY%20YE%20-%20e.pdf |
| work_keys_str_mv | AT yeyeemay expansioncharacterisationanddifferentiationofhumanneuralstemcells |