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Journal of Biomedical Research | ISSN: 0976-1683 | Volume 30

allied

academies

March 14-15, 2019 | London, UK

T issue Engineer ing, Stem Cel ls and Regenerat ive Medicine

Cel l and Gene Therapy

World Congress on

International Conference on

&

Joint Event

A

dult stem cells of mesodermal origin differentiate

into other tissues such as cartilage and bone, when

treated with specialised induction media

in vitro

. However,

transdifferentiating adipose stem cells (ASCs) to other dermal

layers is a challenge to researchers and therapists in regenerative

medicine. Current activities in phototherapy are focused in

optimizing the biological activities of lasers or light on stem

cells including human immortalized ASCs (iASCs). A growing

body of literature suggests that low intensity laser irradiation

(LILI) increase stem cell migration, stimulates proliferation and

possibly differentiates them to other cell types. This study used

a combination of biological and physical inducers for increasing

the differentiation of neurons in culture models. It has used a

combination of growth inducers to differentiate iASCs to free-

floating neural stem cells called neurospheres. Further, it has

applied near infrared (NIR) lasers of wavelength 825nm with

fluences ranging from 5 to 15 J/cm

2

on these neurospheres.

Changes in the metabolic and redox status of these newly

differentiated neurons were gauged from transcriptome.

Moreover, neuronal differentiation was determined by

immunostainingusingearlyandlatemarkers.Thisstudywasable

to generate neurospheres from iASCs and differentiate them to

neuronal cells

in vitro

. There was a sharp distinction between

the metabolic processes of these iASCs with the primary ASCs.

Strikingly, therewas an increase in an early neuronal marker at 5

J/cm

2

and 15 J/cm

2

signifying the biphasic dose response of NIR

laser on living systems. Thus, LILI increased the yield of neurons

and effected stem cell differentiation through modulation of

cellular redox status. However, these differentiated cells failed

to express late neuronal markers. This study found that iASCs,

which has the capacity to proliferate indefinitely in culture

medium is an excellent model for differentiation. It gives an

insight into the cellular and molecular events during neuronal

differentiation of iASCs by growth factors and LILI. Further, it has

identified themode of action of NIR laser in differentiating iASCs

to other cell types. The outcome of this study has to be taken

forward for validation by functionality testing and analysis.

Speaker Biography

Heidi Abrahamse is currently the director of the laser research centre, University

of Johannesburg and Department of Science and Technology/National Research

Foundation SARChI chair for laser applications in health. Her research interests

include photobiology and photochemistry with specific reference to photodynamic

cancer therapy, stem cell differentiation and wound healing. She has supervised 40

masters; 15 doctorates and 12 post-doctorate fellows and has published over 150

peer reviewed accredited journal publications, 42 accredited full paper proceedings

and 11 chapters. She serves on the editorial boards of 8 peer-reviewed internationally

accredited journals while acting as reviewer for over 30 journals. She is also the co-

editor in chief of the international accredited journal photomedicine and laser surgery.

e:

habrahamse@uj.ac.za

Heidi Abrahamse

University of Johannesburg, South Africa

Laser-induced differentiation of immortalized adipose stem cells to neuronal cells

Heidi Abrahamse

, Biomed Res, Volume 30

DOI: 10.4066/biomedicalresearch-C1-024