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Sera from type 2 (non-insulin-dependent) diabetic and healthy subjects contain different amounts of a very low molecular weight growth peptide for vascular cells.

作者信息

Koschinsky T, Bünting C E, Rütter R, Gries F A

出版信息

Diabetologia. 1985 Apr;28(4):223-8. doi: 10.1007/BF00282237.

DOI:10.1007/BF00282237
PMID:4018449
Abstract

Diabetic angiopathy may be due, in part, to increased growth in vascular cells. We have investigated serum growth factors in Type 2 (non-insulin-dependent) diabetic and healthy subjects and their effect on cultured human arterial smooth muscle cells and fibroblasts. Removal of the dialyzable serum fraction (mol. wt. less than 12,000) reduced the growth effect of the diabetic sera by 37% (2p less than 0.005) and of the non-diabetic sera by only 8% (2p less than 0.01). In contrast, there was no difference in growth stimulation between the dialyzed diabetic or non-diabetic sera. Complete recovery of the dialyzable serum growth fraction was also obtained at a mol. wt. below 3,500. Ten times the concentration of the low molecular weight growth factor (mol. wt. less than 3,500) from diabetic sera stimulated growth of fibroblasts or arterial smooth muscle cells by a mean of 243% or 174% and from non-diabetic sera by a mean of 146% or 137%, respectively (2p less than 0.01). The growth stimulating potency of this serum fraction (mol. wt. less than 3,500) contained in 10% diabetic sera, was two to ten times higher than that of human growth hormone or insulin, added in amounts equivalent to 10% or physiological serum concentrations. This diabetic serum growth factor was further characterized by: (1) linear dependence of growth stimulation over a concentration range of twenty times and by (2) reduction of the growth stimulating activity to control levels by pretreatment: (a) at 95 degrees C for 30 min, or (b) with two different proteases: Serva pronase E (Streptomyceus griseus) or Calbiochem protease (Subtilisin calsberg).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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1
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Diabetologia. 1985 Apr;28(4):223-8. doi: 10.1007/BF00282237.
2
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Effect of LDL and serum from diabetic subjects on DNA synthesis in HIT-cells in culture.低密度脂蛋白及糖尿病患者血清对培养的HIT细胞中DNA合成的影响。
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本文引用的文献

1
Increased growth stimulation of fibroblasts from diabetics by diabetic serum factors of low molecular weight.低分子量糖尿病血清因子对糖尿病患者成纤维细胞生长刺激作用增强。
Atherosclerosis. 1980 Oct;37(2):311-7. doi: 10.1016/0021-9150(80)90017-9.
2
Regulation of diabetic serum growth factors for human vascular cells by the metabolic control of diabetes mellitus.
Atherosclerosis. 1981 Jun;39(3):313-9. doi: 10.1016/0021-9150(81)90018-6.
3
Glucose inhibits replication of cultured human endothelial cells.葡萄糖抑制培养的人内皮细胞的复制。
Diabetologia. 1982 Nov;23(5):436-9. doi: 10.1007/BF00260958.
4
Serum low density lipoproteins with mitogenic effect on cultured aortic smooth muscle cells.
Atherosclerosis. 1982 Feb;41(2-3):171-83. doi: 10.1016/0021-9150(82)90183-6.
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Blood glucose and atherosclerosis.血糖与动脉粥样硬化。
Arteriosclerosis. 1981 Jul-Aug;1(4):227-34. doi: 10.1161/01.atv.1.4.227.
6
Differential responsiveness to insulin of endothelial and support cells from micro- and macrovessels.微血管和大血管的内皮细胞及支持细胞对胰岛素的反应差异
J Clin Invest. 1983 Apr;71(4):974-9. doi: 10.1172/jci110852.
7
Atherosclerosis and the arterial smooth muscle cell: Proliferation of smooth muscle is a key event in the genesis of the lesions of atherosclerosis.动脉粥样硬化与动脉平滑肌细胞:平滑肌增殖是动脉粥样硬化病变发生过程中的关键事件。
Science. 1973 Jun 29;180(4093):1332-9. doi: 10.1126/science.180.4093.1332.
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Blood-sugar and arterial disease.血糖与动脉疾病。
Lancet. 1965 Sep 11;2(7411):505-8. doi: 10.1016/s0140-6736(65)91470-4.
9
Growth of rabbit aortic smooth-muscle cells cultured in media containing diabetic and hyperlipemic serum.在含有糖尿病和高脂血症血清的培养基中培养的兔主动脉平滑肌细胞的生长情况。
Diabetes. 1976 Mar;25(3):207-15. doi: 10.2337/diab.25.3.207.
10
Polypeptides with nonsuppressible insulin-like and cell-growth promoting activities in human serum: isolation, chemical characterization, and some biological properties of forms I and II.人血清中具有不可抑制的胰岛素样和促进细胞生长活性的多肽:I型和II型的分离、化学特性及一些生物学性质
Proc Natl Acad Sci U S A. 1976 Jul;73(7):2365-9. doi: 10.1073/pnas.73.7.2365.