Tezin Türü: Yüksek Lisans
Tezin Yürütüldüğü Kurum: Pamukkale Üniversitesi, Fen-Edebiyat Fakültesi, Biyoloji Bölümü, Türkiye
Tezin Onay Tarihi: 2018
Tezin Dili: Türkçe
Öğrenci: Kemal Ertosun
Danışman: Alaattin Şen
Özet:
Most of the current knowledge and the research on multiple sclerosis is
based on data obtained from the experimental allergic encephalomyelitis
(EAE) model. The factors that play a crucial role in cell migration into
the central nervous system are being investigated for development of
and new treatments. Leukocyte infiltration into the CNS occurs in
diseases such as multiple sclerosis (MS) and is responsible for
degenerative inflammatory pathologies. Hence, the analysis of leukocyte
populations infiltrated into the CNS is a frequent examination for
understanding the pathogenic mechanisms of MS and for therapeutic
purposes. In this study, a total of 50 C57BL6 mice at the age of 6-8
week were used to develop EAE by subcutaneous injection of the MOG35-55
peptide in complete Freud's adjuvant. Ten healthy mice of same age and
strain were used as a control group. After induction of EAE (3.5 ± 0.5
clinical score) brain tissues were removed. Leucocytes were isolated
applying density gradient centrifugation from brain tissues. CD45, CD3,
Ly6G, Ly6C, CD11b expressions at cell surfaces were detected using
specific antibodies at both control and EAE mice by flow cytometric
analysis. The results have shown that there was no statistical
difference among the animals in the CD45-bright Ly6G groups, but a
significant increase in the CD11b+-Ly6C cells in EAE mice compared to
healthy groups were observed. Our findings have shown that the leukocyte
infiltration into the CNS plays a role in the pathogenesis of EAE and
could be used to follow the progression of EAE.