Neural stem/progenitor cells from adult canine cervical spinal cord have the potential to differentiate into neural lineage cells

被引:2
作者
Kim, Woo Keyoung [1 ,2 ,3 ]
Son, Yeon Sung [4 ]
Lim, Ji-Hey [5 ]
Kim, Wan Hee [1 ,2 ]
Kang, Byung-Jae [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Dept Vet Clin Sci, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Vet Sci, Seoul 08826, South Korea
[3] Seoul Natl Univ, BK21 FOUR Future Vet Med Leading Educ & Res Ctr, Seoul 08826, South Korea
[4] Seoul Natl Univ, Coll Med, Med Res Ctr, Seoul 03080, South Korea
[5] Univ Missouri, Coll Vet Med, Dept Neurol Neurosurg, Columbia, MO 65211 USA
关键词
Neural progenitor cells; Dogs; Neurospheres; Differentiation; STEM-CELLS; FUNCTIONAL RECOVERY; MICROENVIRONMENT; TRANSPLANTATION; REHABILITATION; NEUROSPHERE; EXPRESSION; PRECURSOR; NEURONS; CULTURE;
D O I
10.1186/s12917-023-03757-3
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background center dot Neural stem/progenitor cells (NSPCs) are multipotent self-renewing cells that can be isolated from the brain or spinal cord. As they need to be isolated from neural tissues, it is difficult to study human NSPCs. To facilitate NSPC research, we attempted to isolate NSPCs from dogs, as dogs share the environment and having many similar diseases with humans. We collected and established primary cultures of ependymal and subependymal cells from the central canal of the cervical spinal cord of adult dogs. To isolate pure NSPCs, we employed the monolayer culture and selective medium culture methods. We further tested the ability of the NSPCs to form neurospheres (using the suspension culture method) and evaluated their differentiation potential.Results center dot The cells had the ability to grow as cultures for up to 10 passages; the growth curves of the cells at the 3rd, 6th, and 9th passages showed similar patterns. The NSPCs were able to grow as neurospheres as well as monolayers, and immunostaining at the 3rd, 6th, and 9th passages showed that these cells expressed NSPC markers such as nestin and SOX2 (immunofluorescent staining). Monolayer cultures of NSPCs at the 3rd, 6th, and 9th passages were cultured for approximately 14 days using a differentiation medium and were observed to successfully differentiate into neural lineage and glial cells (astrocytes, neurons, and oligodendrocytes) at all the three passages tested.Conclusion center dot It is feasible to isolate and propagate (up to at least 10 passages) canine cervical spinal cord-derived NSPCs with the capacity to differentiate into neuronal and glial cells. To the best of our knowledge this is the first study to successfully isolate, propagate, and differentiate canine NSPCs derived from cervical spinal cord in the adult canine, and we believe that these cells will contribute to the field of spinal cord regeneration in veterinary and comparative medicine.
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