Title

TGF-beta 1 expression is reduced in hydrocephalic H-Tx rat brain

Authors

Authors

X. Cai; J. V. Pattisapu; R. W. Tarnuzzer; C. Fernandez-Valle;J. S. Gibson

Comments

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Abbreviated Journal Title

Eur. J. Pediatr. Surg.

Keywords

H-Tx rat; hydrocephalus; transforming growth factor-beta 1 (TFF-beta 1); RT-PCR; gene expression; TRANSFORMING GROWTH FACTOR-BETA-1; EXTRACELLULAR-MATRIX COMPONENTS; CENTRAL-NERVOUS-SYSTEM; CONGENITAL HYDROCEPHALUS; COMMUNICATING; HYDROCEPHALUS; MICE; GROWTH-FACTOR-BETA-1; DISEASE; INJURY; MODELS; Pediatrics; Surgery

Abstract

Transforming growth factor-beta 1 (TGF-beta 1) is a cytokine with diverse biological effects. Overexpression of TGF-beta 1 in mice has been shown to induce progressive hydrocephalus. We have used a quantitative RT-PCR method to analyze the TGF-beta 1 expression in the brains of H-Tx rat, a model of congenital hydrocephalus. our studies have shown that rather than increased expression, the 3- and 10-day hydrocephalic H-Tx rats have significantly lower TGF-beta 1 levels than their normal siblings (p < 0.01). This difference became insignificant in the 21-day group. Besides, both hydrocephalic and normal H-Tx rats have significantly lower TGF-beta 1 levels in all three age groups of 3-, 10- and 21-days than SD control rats (p < 0.01 in all three groups) although the difference tends to become less significant with development. We also tested the expression of another cytokine, the epidermal growth factor, and observed a similar reduction. This suggests that the TGF-beta 1 expression change is not unique to the development of hydrocephalus in this rat model; Our hypothesis is that the TCF-beta 1 expression decrease in the H-Tx rat is not the cause of the disease. Rather it might be the result of feedback inhibition by increase in the expression of the gene it regulates, including an extracellular matrix component. Effort is currently being made to test this hypothesis.

Journal Title

European Journal of Pediatric Surgery

Volume

9

Publication Date

1-1-1999

Document Type

Article; Proceedings Paper

Language

English

First Page

35

Last Page

38

WOS Identifier

WOS:000084656200013

ISSN

0939-7248

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