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组织免疫染色法用于研究再生鳍中的蛋白质表达和细胞增殖。

Section Immunostaining for Protein Expression and Cell Proliferation Studies of Regenerating Fins.

机构信息

Institute of Molecular Biology, University of Oregon, Eugene, OR, USA.

Department of Biology, University of Oregon, Eugene, OR, USA.

出版信息

Methods Mol Biol. 2024;2707:235-254. doi: 10.1007/978-1-0716-3401-1_16.

Abstract

Adult zebrafish fins fully regenerate after resection, providing a highly accessible and remarkable vertebrate model of organ regeneration. Fin injury triggers wound epidermis formation and the dedifferentiation of injury-adjacent mature cells to establish an organized blastema of progenitor cells. Balanced cell proliferation and redifferentiation along with cell movements then progressively reestablish patterned tissues and restore the fin to its original size and shape. A mechanistic understanding of these coordinated cell behaviors and transitions requires direct knowledge of proteins in their physiological context, including expression, subcellular localization, and activity. Antibody-based staining of sectioned fins facilitates such high-resolution analyses of specific, native proteins. Therefore, such methods are mainstays of comprehensive, hypothesis-driven fin regeneration studies. However, section immunostaining requires labor-intensive, empirical optimization. Here, we present detailed, multistep procedures for antibody staining and co-detecting proliferating cells using paraffin and frozen fin sections. We include suggestions to avoid common pitfalls and to streamline the development of optimized, validated protocols for new and challenging antibodies.

摘要

成年斑马鱼的鳍在切除后可以完全再生,为器官再生提供了一个高度可及且显著的脊椎动物模型。鳍损伤会触发伤口表皮的形成,并使损伤相邻的成熟细胞去分化,从而建立一个有组织的祖细胞胚基。然后,通过平衡细胞增殖和再分化以及细胞运动,逐渐重新建立有图案的组织,并将鳍恢复到原来的大小和形状。要了解这些协调的细胞行为和转变的机制,需要直接了解生理环境中的蛋白质,包括表达、亚细胞定位和活性。对切片鳍进行基于抗体的染色有助于对特定的天然蛋白质进行高分辨率分析。因此,这些方法是全面的、基于假设的鳍再生研究的基础。然而,切片免疫染色需要劳动密集型的、经验性的优化。在这里,我们介绍了使用石蜡和冰冻鳍切片进行抗体染色和共检测增殖细胞的详细多步程序。我们还包括了一些避免常见陷阱和简化针对新的和具有挑战性的抗体开发优化、验证方案的建议。

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