Porcine skeletal muscle typing in histochemical and in-situ RT-PCR analysis

IF 1.9 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE Veterinary and Animal Science Pub Date : 2024-03-01 DOI:10.1016/j.vas.2023.100332
Tao Lin , Zhun Liu , Fawen Dai , Hechuan Wang , Jianjun Zuo
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Abstract

Currently, there are plenty of histochemical methods to classify pig muscle fibers, which confused the naming and classification of muscle fibers. This study aims to analyze the difference and correlation of 6 different histochemical methods and select the most suitable method for muscle fiber classification at the molecular and histomological levels by in-situ RT-PCR and enzyme histochemical methods. Muscle fiber samples, including psoas (PM), semitendinosus (SM) and trapezius muscle (TM), were collected from Large Spotted (LS), Lantang (LT) and Landrace (LR) pigs at their market-ages (LS at 150 d, LT at 210 d, and LR at 150 d). 6 kinds of histochemical methods combining actomyosin adenosine triphosphatase (AM-ATPase) with succinate dehydrogenase (SDH) enzyme were conducted to differentiate fiber types. 2 types of fibers (I and II) were differentiated by acid 2-fibre (2-AC) or alkaline 2-fibre classification(2-AL), 3 types of fibers (βR, αR and αW) by 3-AC or 3-AL, and 4 types of fibers (I, IIa, IIx and IIb) by 4-AC, or 4-AL. Results showed that AC and AL muscle-fiber classification were consistent in reflecting the characteristics of muscle fibers(P > 0.05), but the color of each muscle fiber type was just opposite. AC methods may be superior to AL methods because of their clear staining background, the sensitivity to staining condition. But there were breed differences and tissue specificity in the optimal preincubation condition. The optimal acid preincubation condition for classifying muscle fibers was pH4.30 for LT, while pH 4.35 for the LS and LR pigs. Meanwhile the optimal acid preincubation condition was pH4.35 for PM, while pH4.40 for TM or SM. For further selection from 2, 3, 4-AC, in-situ RT-PCR was applied to detect the mRNA distribution of myosin heavy chain I (MyHC-I). By combining in-situ PCR with enzyme histochemistry methods, MyHC-I gene and its product – Type I fibrocytes were directly located in cells at both molecular level and morphological level. Compared with the cross-sectional area (CSA) of different muscle fibers (i.e. I, II, βR, αR, αW, IIa, IIx and IIb) identified by enzyme histochemistry, it was found that the CSAs with stronger mRNA expression signal of MyHC-Ⅰ were closer to those of the Type I muscle fiber measured by 4-AC enzyme histochemistry (P > 0.05). Therefore, 4-AC may be considered as the most proper muscle typing method to study muscle fiber typing as well as meat quality. And the combination of in-situ RT-PCR and histochemistry may help better understand porcine muscle fiber characteristics and meat quality in pigs.

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组织化学和原位 RT-PCR 分析中的猪骨骼肌分型
目前,猪肌纤维分类的组织化学方法很多,混淆了肌纤维的命名和分类。本研究旨在通过原位 RT-PCR 和酶组织化学方法,分析 6 种不同组织化学方法的差异和相关性,从分子和组织学层面选择最适合的方法进行肌纤维分类。从大斑猪(LS)、兰塘猪(LT)和陆地猪(LR)的上市年龄(LS 150 d、LT 210 d 和 LR 150 d)采集肌肉纤维样品,包括腰肌(PM)、半腱肌(SM)和斜方肌(TM)。结合肌动蛋白腺苷三磷酸酶(AM-ATPase)和琥珀酸脱氢酶(SDH)的 6 种组织化学方法来区分纤维类型。通过酸性2-纤维(2-AC)或碱性2-纤维(2-AL)来区分2种纤维(I和II),通过3-AC或3-AL来区分3种纤维(βR、αR和αW),通过4-AC或4-AL来区分4种纤维(I、IIa、IIx和IIb)。结果表明,AC 和 AL 肌纤维分类法在反映肌纤维特征方面具有一致性(P > 0.05),但各肌纤维类型的颜色正好相反。AC方法可能优于AL方法,因为其染色背景清晰,对染色条件敏感。但最佳预孵育条件存在品种差异和组织特异性。LT猪肌纤维分类的最佳酸预孵育条件为pH4.30,而LS猪和LR猪的最佳酸预孵育条件为pH4.35。同时,PM 的最佳酸预培养条件为 pH4.35,而 TM 或 SM 的最佳酸预培养条件为 pH4.40。为了进一步从 2、3、4-AC 中进行筛选,采用了原位 RT-PCR 技术检测肌球蛋白重链 I(MyHC-I)的 mRNA 分布。通过将原位 PCR 与酶组织化学方法相结合,从分子水平和形态水平直接定位了细胞中的 MyHC-I 基因及其产物--I 型纤维细胞。与酶组织化学鉴定的不同肌纤维(即Ⅰ、Ⅱ、βR、αR、αW、Ⅱa、Ⅱx和Ⅱb)的横截面积(CSA)相比,发现MyHC-Ⅰ的mRNA表达信号更强的CSA与4-AC酶组织化学测定的Ⅰ型肌纤维的CSA更接近(P >0.05)。因此,4-AC 可被视为研究肌纤维分型和肉质的最合适的肌肉分型方法。原位 RT-PCR 与组织化学的结合有助于更好地了解猪的肌纤维特征和肉质。
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来源期刊
Veterinary and Animal Science
Veterinary and Animal Science Veterinary-Veterinary (all)
CiteScore
3.50
自引率
0.00%
发文量
43
审稿时长
47 days
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