Graduate School of Bio-Application and Systems Engineering, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Arch Insect Biochem Physiol. 2023 Sep;114(1):e22032. doi: 10.1002/arch.22032. Epub 2023 Jul 10.
To regulate physiological homeostasis and behavior in Bombyx mori, more than 20 peptide hormones in the midgut of larvae are secreted upon detection of food substances at the lumen. Although it is logical to assume that the timings of peptide hormone secretions are regulated, little is known about the mechanisms. In this study, the distributions of enteroendocrine cells (EECs) producing five peptide hormones and EECs expressing gustatory receptors (Grs), as candidate receptors for luminal food substances and nutrients, were examined via immunostaining in B. mori larvae. Three patterns of peptide hormone distribution were observed. Tachykinin (Tk)- and K5-producing EECs were located throughout the midgut; myosuppressin-producing EECs were located in the middle-to-posterior midgut; and allatostatin C- and CCHamide-2-producing EECs were located in the anterior-to-middle midgut. BmGr4 was expressed in some Tk-producing EECs in the anterior midgut, where food and its digestive products arrived 5 min after feeding began. Enzyme-linked immunosorbent assay (ELISA) revealed secretion of Tk starting approximately 5 min after feeding began, suggesting that food sensing by BmGr4 may regulate Tk secretion. BmGr6 was expressed in a few Tk-producing EECs in the middle-to-posterior midgut, although its significance was unclear. BmGr6 was also expressed in many myosuppressin-producing EECs in the middle midgut, where food and its digestive products arrived 60 min after feeding began. ELISA revealed secretion of myosuppressin starting approximately 60 min after feeding began, suggesting that food sensing by BmGr6 may regulate myosuppressin secretion. Finally, BmGr9 was expressed in many BmK5-producing EECs throughout the midgut, suggesting that BmGr9 may function as a sensor for the secretion of BmK5.
为了调节家蚕幼虫的生理内稳态和行为,当腔肠内检测到食物物质时,会分泌超过 20 种肽激素。虽然假设肽激素的分泌时间受到调节是合乎逻辑的,但对于这些机制知之甚少。在这项研究中,通过免疫染色检查了产生五种肽激素的肠内分泌细胞(EEC)和表达味觉受体(Grs)的 EEC 的分布,Grs 作为腔肠内食物物质和营养素的候选受体。在家蚕幼虫的中肠中观察到三种肽激素分布模式。速激肽(Tk)和 K5 产生 EEC 位于整个中肠;肌抑制素产生 EEC 位于中后中肠;阿塔斯丁 C 和 CCHamide-2 产生 EEC 位于前中肠。BmGr4 在中肠前区的一些 Tk 产生 EEC 中表达,食物及其消化产物在进食开始后 5 分钟到达那里。酶联免疫吸附测定(ELISA)显示 Tk 的分泌大约在进食开始后 5 分钟开始,表明 BmGr4 对食物的感知可能调节 Tk 的分泌。BmGr6 在中后区的少数 Tk 产生 EEC 中表达,但意义尚不清楚。BmGr6 也在家蚕肌抑制素产生 EEC 中表达,这些 EEC 位于中肠中部,食物及其消化产物在进食开始后 60 分钟到达那里。ELISA 显示肌抑制素的分泌大约在进食开始后 60 分钟开始,表明 BmGr6 对食物的感知可能调节肌抑制素的分泌。最后,BmGr9 在整个中肠的许多 BmK5 产生 EEC 中表达,表明 BmGr9 可能作为 BmK5 分泌的传感器发挥作用。