Gene Expression Profile of the Hypothalamus in DNP-KLH Immunized Mice Following Electroacupuncture Stimulation

Author:

Kim Sun Kwang123,Kim Jeungshin4,Ko Eunjung1,Kim Hyunseong1,Hwang Deok-Sang5,Lee Sanghoon4,Baek Yonghyeon4,Min Byung-Il6,Nam Sangsoo4,Bae Hyunsu12

Affiliation:

1. Department of Physiology, College of Oriental Medicine, Kyung Hee University, #1 Hoegi-dong, Dongdaemoon-gu, Seoul 130-701, Republic of Korea

2. BK21 Oriental Medical Science Center, Republic of Korea

3. Acupuncture & Meridian Science Research Center, Republic of Korea

4. Department of Acupuncture & Moxibustion, College of Oriental Medicine, Kyung Hee University, #1 Hoeki-dong, Dongdaemoon-gu, Seoul, 130-701, Republic of Korea

5. Department of Oriental Gynecology, College of Oriental Medicine, Republic of Korea

6. Department of Physiology, College of Medicine, Kyung Hee University, Seoul, Republic of Korea

Abstract

Clinical evidence indicates that electroacupuncture (EA) is effective for allergic disorder. Recent animal studies have shown that EA treatment reduces levels of IgE and Th2 cytokines in BALB/c mice immunized with 2,4-dinitrophenylated keyhole limpet protein (DNP-KLH). The hypothalamus, a brain center of the neural-immune system, is known to be activated by EA stimulation. This study was performed to identify and characterize the differentially expressed genes in the hypothalamus of DNP-KLH immunized mice that were stimulated with EA or only restrained. To this aim, we conducted a microarray analysis to evaluate the global gene expression profiles, using the hypothalamic RNA samples taken from three groups of mice: (i) normal control group (no treatments); (ii) IMH group (DNP-KLH immunization + restraint); and (iii) IMEA group (immunization + EA stimulation). The microarray analysis revealed that total 39 genes were altered in their expression levels by EA treatment. Ten genes, including T-cell receptor alpha variable region family 13 subfamily 1 (Tcra-V13.1), heat shock protein 1B (Hspa1b) and 2–5oligoadenylate synthetase 1F (Oas1f), were up-regulated in the IMEA group when compared with the IMH group. In contrast, 29 genes, including decay accelerating factor 2 (Daf2), NAD(P)H dehydrogenase, quinone 1 (Nqo1) and programmed cell death 1 ligand 2 (Pdcd1lg2) were down-regulated in the IMEA group as compared with the IMH group. These results suggest that EA treatment can modulate immune response in DNP-KLH immunized mice by regulating expression levels of genes that are associated with innate immune, cellular defense and/or other kinds of immune system in the hypothalamus.

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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