Coast Geoffrey M, Garside Christopher S, Webster Simon G, Schegg Kathleen M, Schooley David A
Department of Biology, Birkbeck (University of London), London WC1E 7HX, UK.
J Exp Biol. 2005 Sep;208(Pt 17):3281-91. doi: 10.1242/jeb.01760.
Mosquito natriuretic peptide (MNP), an uncharacterised peptide from the yellow fever mosquito, Aedes aegypti, acts via cyclic AMP to stimulate secretion of Na+-rich urine by opening a Na+ conductance in the basolateral membrane of Malpighian tubule principal cells. Corticotropin releasing factor (CRF)-related peptides and calcitonin (CT)-like diuretic peptides use cyclic AMP as a second messenger and were therefore considered likely candidates for MNP. BLAST searches of the genome of the malaria mosquito Anopheles gambiae, gave sequences for the CRF-related peptide Anoga-DH44 and the CT-like peptide Anoga-DH31, which were synthesised and tested for effects on Malpighian tubules from An. gambiae and Ae. aegypti, together with 8-bromo-cyclic AMP. The cyclic AMP analogue stimulated secretion of Na+-rich urine by An. gambiae Malpighian tubules, reproducing the response to MNP in Ae. aegypti. It also depolarised the principal cell basolateral membrane voltage (Vb) while hyperpolarising the transepithelial voltage (Vt) to a similar extent. Anoga-DH4) and Anoga-DH31 stimulated production of cyclic AMP, but not cyclic GMP, by Malpighian tubules of An. gambiae. Both peptides had diuretic activity, but only Anoga-DH31 had natriuretic activity and stimulated fluid secretion to the same extent as 8-bromo-cyclic AMP. Likewise, Anoga-DH31 reproduced the effects of cyclic AMP on tubule electrophysiology, whereas Anoga-DH44 initially hyperpolarised Vb and depolarised Vt, which is the opposite of the effect of Anoga-DH31. Anoga-DH44 and Anoga-DH31 were also tested for effects on fluid secretion and ion transport by Ae. aegypti tubules. As in An. gambiae, the CRF-related peptide Anoga-DH44 had a non-specific effect on the transport of Na+ and K+, whereas the CT-like peptide Anoga-DH31 specifically stimulated transepithelial Na+ transport. We conclude that the CT-like peptide Anoga-DH31 is the previously uncharacterised mosquito natriuretic peptide.
蚊子利尿钠肽(MNP)是一种来自黄热病蚊子埃及伊蚊的未被鉴定的肽,它通过环磷酸腺苷(cAMP)起作用,通过打开马尔皮基氏小管主细胞基底外侧膜中的钠电导来刺激富含钠的尿液分泌。促肾上腺皮质激素释放因子(CRF)相关肽和降钙素(CT)样利尿肽使用环磷酸腺苷作为第二信使,因此被认为可能是MNP的候选者。对疟疾蚊子冈比亚按蚊的基因组进行BLAST搜索,得到了CRF相关肽Anoga-DH44和CT样肽Anoga-DH31的序列,将它们合成并测试其对冈比亚按蚊和埃及伊蚊的马尔皮基氏小管的影响,同时加入8-溴环磷酸腺苷。环磷酸腺苷类似物刺激冈比亚按蚊马尔皮基氏小管分泌富含钠的尿液,重现了埃及伊蚊对MNP的反应。它还使主细胞基底外侧膜电压(Vb)去极化,同时使跨上皮电压(Vt)超极化到类似程度。Anoga-DH44和Anoga-DH31刺激冈比亚按蚊马尔皮基氏小管产生环磷酸腺苷,但不产生环鸟苷酸。两种肽都有利尿活性,但只有Anoga-DH31有利尿钠活性,并且刺激液体分泌的程度与8-溴环磷酸腺苷相同。同样,Anoga-DH31重现了环磷酸腺苷对小管电生理学的影响,而Anoga-DH44最初使Vb超极化并使Vt去极化,这与Anoga-DH31的作用相反。还测试了Anoga-DH44和Anoga-DH31对埃及伊蚊小管液体分泌和离子转运的影响。与冈比亚按蚊一样,CRF相关肽Anoga-DH44对钠和钾的转运有非特异性影响,而CT样肽Anoga-DH31特异性刺激跨上皮钠转运。我们得出结论,CT样肽Anoga-DH31是先前未被鉴定的蚊子利尿钠肽。