## Abstract When chicken serum was added to serum‐deprived quiescent cultures of chick embryo fibroblasts the activity of amino acid transport by means of the A system, as measured by α‐aminoisobutyric acid and L‐proline uptake after discrimination of the contribution of interacting systems, increa
Involvement of membrane sulfhydryls in the activation and maintenance of nutrient transport in chick embryo fibroblasts
✍ Scribed by Smith-Johannsen, H. ;Perdue, J. F. ;Ramjeesingh, M. ;Kahlenberg, A.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1977
- Tongue
- English
- Weight
- 668 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0091-7419
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✦ Synopsis
Abstract
At 5 μg/ml, insulin stimulates hexose, A‐system amino acid, and nucleoside transport by serum‐starved chick embryo fibroblasts (CEF). This stimulation, although variable, is comparable to that induced by 4% serum. The sulfhydryl oxidants diamide (1–20 μM). hydrogen peroxide (500 μM), and methylene blue (50 μM) mimic the effect of insulin in CEF.
PCMB‐S,^1^ a sulfhydryl‐reacting compound which penetrates the membrane slowly, has a complex effect on nutrient transport in serum‐ and glucose‐starved CEF. Hexose uptake is inhibited by 0.1–1 mM PCMB‐S in a time‐ and concentration‐dependent manner, whereas A‐system amino acid transport is inhibited maximally within 10 min of incubation and approaches control rates after 60 min. A differential sensitivity of CEF transport systems is also seen in cells exposed to membrane‐impermeant glutathione‐maleimide I, designated GS‐Mal. At 2 mM GS‐Mal reduces the rate of hexose uptake 80–100% in serum‐ and glucose‐starved CEF; in contrast A‐system amino acid uptake is unaffected. D‐glucose, but not L‐glucose or cytochalasin B, protects against GS‐Mal inhibition. These results are consistent with the hypothesis that sulfhydryl groups are involved in nutrient transport and that those sulfhydryls associated with the hexose transport system and essential for its function are located near the exofacial surface of the membrane in CEF.
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