激素切换小岛细胞:与发射器切换神经元平行
Yuval Dor1, Nicholas C Spitzer2
1Department of Developmental Biology and Cancer Research, The Institute for Medical Research Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Frontiers in cell and developmental biology
|May 13, 2025
概括
胰腺小岛细胞和神经元,尽管有不同的起源,共享相似之处. 它们独特的可塑性机制 - - 岛细胞中的激素表达和神经元中神经递质的切换 - - 可能源自一个古老的分子电路,为细胞适应性提供了洞察力.
科学领域:
- 细胞生物学 细胞生物学
- 神经科学是一个神经科学.
- 内分泌学 在内分泌学.
背景情况:
- 胰腺小岛细胞和神经元表现出生理和分子相似性.
- 这两种细胞类型都通过电压依赖机制释放生物活性分子.
- 共享的转录因子和结构基因突出显示了分子的共同点.
研究的目的:
- 提出神经元中的神经递质切换和小岛细胞中的多激素表达具有共同的分子基础.
- 为了研究这些独特的细胞类型中细胞可塑性的基础古代分子电路的潜力.
- 为了比较岛屿细胞中的动态激素表达与神经元中的发射器切换,以获得功能和机械的见解.
主要方法:
- 细胞可塑性机制的比较分析.
- 研究胰腺小岛细胞中的动态激素表达模式.
- 检查神经递质在神经元中的切换现象.
- 关于小岛细胞和神经元之间的分子和生理相似性的文献综述.
主要成果:
- 确定了小岛细胞中的荷尔蒙表达动态和神经元中神经递质切换之间的深刻相似性.
- 突出了潜在的共享古老的分子电路,控制细胞可塑性.
- 在这两种细胞类型之间建立了功能和分子平行.
结论:
- 神经递质切换和多激素表达可能代表细胞可塑性的保存机制.
- 平行理解这些现象可以阐明细胞适应性的基本原理.
- 这种比较为我们提供了对两种细胞类型中生物活性分子释放的调节和功能的新见解.
相关概念视频
Glucose Homeostasis: Pancreatic Islets and Insulin Secretion
1.0K
The pancreatic islets comprising only 1%-2% of the volume are highly vascularized and innervated mini-organs. They contain five endocrine cell types, including β cells that secrete insulin, which is synthesized as a single polypeptide chain, preproinsulin, processed to proinsulin, and finally to insulin and C-peptide. This process is complex and regulated, involving the Golgi complex, the endoplasmic reticulum, and the secretory granules of the β cell.
Insulin and C-peptide are...
Insulin and C-peptide are...
1.0K
Regulation of Hormone Secretion
2.9K
Regulation of hormone secretion is a finely tuned orchestration driven by various types of stimuli, encompassing neural, humoral, and hormonal signals. Environmental cues instigate neural stimuli, where action potentials traverse nerve fibers to reach their designated targets. An illustrative scenario is the body's response to stress, wherein the sympathetic nervous system releases epinephrine from the adrenal glands, inducing the well-known 'fight or flight' reaction.
Humoral...
Humoral...
2.9K
Forced Transdifferentiation
1.8K
Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
Artificial...
1.8K
Target Cell Response to Hormones
2.8K
Hormones intricately bind to receptors on the surface or within target cells, initiating a cascade of cellular responses.
Notably, the cellular response can be regulated by altering the number of receptors expressed in the cell. For example, prolonged exposure to elevated hormone levels results in a gradual decline or down-regulation in the number of receptors for that specific hormone on the cell surface. Conversely, in response to low hormone levels, cells may use up-regulation, producing an...
Notably, the cellular response can be regulated by altering the number of receptors expressed in the cell. For example, prolonged exposure to elevated hormone levels results in a gradual decline or down-regulation in the number of receptors for that specific hormone on the cell surface. Conversely, in response to low hormone levels, cells may use up-regulation, producing an...
2.8K
Insulin Secretory Vesicles
4.8K
Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
4.8K
Insulin: The Receptor and Signaling Pathways
1.0K
Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but...
1.0K


