• Users Online: 234
  • Print this page
  • Email this page


 
 
Table of Contents
ORIGINAL ARTICLE
Year : 2022  |  Volume : 10  |  Issue : 1  |  Page : 20-22

Tyrosine hydroxylase-immunopositive cells and melanin in the mesencephalon of yugan black-bone fowl


1 Department of Veterinary Medicine, College of Life Science and Engineering, Foshan University, Foshan 528231, China
2 Department of Veterinary Medicine, College of Life Science and Engineering, Foshan University, Foshan 528231; Department of Veterinary Medicine, College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China

Date of Submission10-Jun-2020
Date of Decision07-Sep-2020
Date of Acceptance18-Sep-2020
Date of Web Publication09-Feb-2021

Correspondence Address:
Prof. Haiquan Zhao
College of Life Science and Engineering, Foshan University, Foshan 528231
China
Dr. Hui Zhang
College of Life Science and Engineering, Foshan University, Foshan 528231
China
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/JMAU.JMAU_50_20

Rights and Permissions
  Abstract 


Background: The Yugan blackbone fowl (YBF) is a special poultry with hyperpigmentation in various organs, including feather. However, the mechanism of hyperpigmentation is limited, and the melanic information of other organs except skin is rare. Aims and Objectives: In this study, we attempt to get an insight of the mechanism of melanogenesis of birds. Materials and Methods: The mesencephalon of YBF was observed by light microscopy with hematoxylineosin and tyrosine hydroxylase (TH) immunohistochemistry. Results: The TH immunopositive cells were found in the mesencephalon. Moreover, the melanin was also observed in the connective tissue of the mesencephalon. Conclusion: Our results confirmed the existence of melanin and TH immunopositive cells in the mesencephalon of YBF. These results provide a reference for further study on the mechanism of melanogenesis/hyperpigmentation in birds.

Keywords: Chicken, immunohistochemistry, melanin, tyrosine hydroxylase


How to cite this article:
Chu M, Liu Y, Si Y, Yu H, Ye Y, Zhao H, Zhang H. Tyrosine hydroxylase-immunopositive cells and melanin in the mesencephalon of yugan black-bone fowl. J Microsc Ultrastruct 2022;10:20-2

How to cite this URL:
Chu M, Liu Y, Si Y, Yu H, Ye Y, Zhao H, Zhang H. Tyrosine hydroxylase-immunopositive cells and melanin in the mesencephalon of yugan black-bone fowl. J Microsc Ultrastruct [serial online] 2022 [cited 2023 Apr 1];10:20-2. Available from: https://www.jmau.org/text.asp?2022/10/1/20/308935




  Introduction Top


The black-bone fowl (BF) is a special poultry because of hyperpigmentation in various organs.[1] Other vertebrate species are also reported to show pigmentation in the viscera.[2],[3] Melanin plays an important role in radioprotective, antioxidation, predator–prey interactions, thermoregulation, disease and parasites resistance, antimicrobial activity, inhibiting virus, and protecting against mitochondrial superoxide generation and mtDNA damage.[4],[5],[6],[7],[8] BF with hyperpigmentation may serve as a potential biological model to study the mechanism of melanogenesis and melanomagenesis.[9] Many studies regarding BF focus on the skin melanogenesis. Previous study has demonstrated the ultrastructure of melanocytes and processes of melanogenesis in the skin of BF.[1] However, the melanic information of other organs is rare. The Yugan black-bone fowl (YBF) belongs to a kind of BF and has also a great mass of melanin in many organs. In particular, their feather is flat and black. It is different from another BF – Taihe silky BF, which has white and silky feather. The Taihe silky BF was frequently studied.[10] However, the investigations of YBF are rare.

Tyrosine hydroxylase (TH) is a rate-limiting enzyme for the biosynthesis of dopamine (DA). TH is a reliable marker for some types of neurons.[11] Further, TH is expressed in the dopaminergic cells, which are involved in melanogenesis.[12],[13] Here, the TH-immunopositive cells and melanin were identified in the mesencephalon of YBF, in an attempt to understand the cytological mechanism of melanogenesis and hyperpigmentation in birds. Further, we might get insight into the pathogenesis of neuromelanin-related disease – for example, Parkinson's disease.[14]


  Materials and Methods Top


Animals

This work had been conducted under the scientific and technical department of Jiangxi Agricultural University after relevant ethical review. The chickens were fed ad libitum for 60 days, drinking-free and comfortable environment. All chickens were sacrificed with ethyl ether. After euthanized, the mesencephalons of the chickens were sampled for section and immunohistochemistry (IHC).

Mesencephalon sections and hematoxylin-eosin staining

A standard procedure in histology was used according to a previous study.[15] The samples of the mesencephalon from the chickens were fixed in Bouin's solution and then washed with 0.1 M phosphate-buffered saline (PBS) (pH 7.4), dehydrated in ethanol, and embedded in paraffin. The 5 μm sections were stained with hematoxylin-eosin for general morphology. The slides were mounted with Permount and analyzed with BM 2000 microscope (Nanjing, China). The micrographs were acquired using ScopeImage 9.0 (H3D) software (Nanjing, China).

Tyrosine hydroxylase immunohistochemistry

After deparaffinating and rehydration, the sections were heated at 95°C for epitope retrieval in citrate buffer (pH 6.0) for 15 min. The sections were treated with 0.3% H2O2. After washing in PBS, the sections were incubated in the normal goat serum at room temperature in a humid chamber for 30 min, and then, they were drained and further incubated in anti-TH antibody (Abcam, USA) (diluted 1:200) overnight at 4°C. The secondary antibody was applied at room temperature for 15 min, and the sections were rinsed and incubated in streptavidin-HRP at room temperature for 15 min. After washing in PBS, the peroxidase was visualized with a diaminobenzidine/hydrogen peroxidase chromogen reaction in the dark room. The sections were visualized with a BM 2000 microscopy (Yongxin, China). The color reaction was ceased by PBS rinse, and then, the sections were counterstained by hematoxylin. The photomicrographs were also acquired using ScopeImage 9.0 (H3D) software (Yongxin, China).


  Results Top


The location of melanin in Yugan black-bone fowl

The YBF was black all over the body [Figure 1]a, [Figure 1]b, [Figure 1]c, [Figure 1]d, including skin [Figure 1]b, muscle, bone, and viscera [Figure 1]c and [Figure 1]d. In particular, the feather was black [Figure 1]a. The melanin was also present in the connective tissue of internal organs [Figure 1]c and [Figure 1]d. In addition, the melanin was present in mesencephalon, cellular gray matter, and connective tissue surrounding the blood vessels [Figure 2]a and [Figure 2]b.
Figure 1: The gross anatomy of Yugan black-bone fowl. The chicken had black flat feather (a). A high amount of melanin was located in the skin (b), muscle (c), bone (c), and viscera (c and d)

Click here to view
Figure 2: A large amount of melanin was located in the mesencephalon of Yugan black-bone fowl. The white arrows denoted the melanin (a and b). Bar: (a) = 50 μm and (b) = 20 μm

Click here to view


Tyrosine hydroxylase immunohistochemistry

IHC results showed that many TH-immunopositive cells located in the ventral mesencephalon [Figure 3]a and [Figure 3]b. The TH-immunopositive cells were stained and showed brown granules with different shade in the cytoplasm. Some processes of TH-immunopositive cells were observed [Figure 3]a and [Figure 3]b. The nuclei of TH-immunopositive cells and neuroglial cells were negative without brown granules. They were stained by hematoxylin and showed blue.
Figure 3: The tyrosine hydroxylase-immunopositive neurons were present in the mesencephalon of Yugan black-bone fowl (a and b). Bar: 20 μm

Click here to view



  Discussion Top


TH is a rate-limiting enzyme of DA synthesis and is also a reliable marker for dopaminergic cells and neuronal cells.[11] TH is located in the dopaminergic cells and neuronal cells of the peripheral system and central nervous system (CNS).[16] TH catalyzes tyrosine conversion into Dopa, which is decarboxylated to DA.[17] DA belongs to catecholamines, which also includes norepinephrine (NE) and epinephrine (E). Moreover, DA can be converted to NE and E.[17] DA can be synthesized in the CNS, but the brain is regarded as a minor source of DA.[18] However, in the present study, TH-immunopositive cells were frequently observed in the ventral mesencephalon of YBF. A previous study showed that neuromelanin has been found only in the dopaminergic neuronal cells in the human brain.[12] The neuromelanin could be synthesized from peptidyl derivatives of DA in which the Cys group of the peptide is linked to DA.[19] In addition, the retinal pigmented epithelium could be a potential source of Dopa, responsible for activating dopaminergic cells before TH synthesis.[13] In the current study, our results demonstrated that TH-immunopositive cells located in the ventral mesencephalon of YBF. It is suggested that the TH-immunopositive dopaminergic cells of the mesencephalon might produce a great deal of DA. Further studies should be done to confirm the suggestion.

Previous studies demonstrated that all catecholamines, including DA, are involved in melanogenesis and pigment aggregation in various species.[20] The catecholamines are possible precursors of neuromelanin, the biosynthesis of which occurs in brain regions containing DA and NE.[21] In particular, DA produced from TH-immunopositive dopaminergic neuronal cells could be as precursor of melanin or induce melanin synthesis directly.[21] DA also provides the cAMP response and promotes melanogenesis in melanocytes via the β2-adrenoceptor signal.[22],[23] DA can also transform into E/NE and induce melanin synthesis.[23] Therefore, TH-immunopositive dopaminergic cells may be involved in the melanogenesis by catecholamines in the mesencephalon of YBF.


  Conclusion Top


In the present study, our results confirmed the existence of melanin and TH-immunopositive cells in the mesencephalon of YBF. It is suggested that TH-immunopositive dopaminergic cells and melanogenesis may be related by catecholamines. The results will contribute to better understand the cytological mechanism of melanogenesis and hyperpigmentation in birds.

Financial support and sponsorship

The work was supported by the National Natural Science Foundation of China (No. 31760716; 31560681), the Project of Jiangxi Province (No. 20151BBF60007; 20171ACB21028) and the Project of Education Department of Jiangxi Province (No. GJJ160418).

Conflicts for interest

There are no conflicts for interest.



 
  References Top

1.
Ortolani-Machado C, De Freitas P, Borges ME, Faraco C. Special features of dermal melanocytes in white silky chicken embryos. Anat Rec (Hoboken) 2008;291:55-64.  Back to cited text no. 1
    
2.
Franco-Belussi L, De Souza Santos LR, Zieri R, De Oliveira C. Visceral pigmentation in three species of the genus Scinax (Anura: Hylidae): Distinct morphological pattern. Anat Rec (Hoboken) 2012;295:298-306.  Back to cited text no. 2
    
3.
Griffing AH, Gamble T, Bauer AM. Distinct patterns of pigment development underlie convergent hyperpigmentation between nocturnal and diurnal geckos (Squamata: Gekkota). BMC Evol Biol 2020;20:40.  Back to cited text no. 3
    
4.
Kim E, Panzella L, Napolitano A, Payne GF. Redox activities of melanins investigated by electrochemical reverse engineering: implications for their roles in oxidative stress. J Invest Dermatol 2020;140:537-43.  Back to cited text no. 4
    
5.
Poulose N, Sajayan A, Ravindran A, Sreechithra TV, Vardhan V, Selvin J, et al. Photoprotective effect of nanomelanin-seaweed concentrate in formulated cosmetic cream: With improved antioxidant and wound healing properties. J Photochem Photobiol B 2020;205:111816.  Back to cited text no. 5
    
6.
Dubey S, Roulin A. Evolutionary and biomedical consequences of internal melanins. Pigment Cell Melanoma Res 2014;27:327-38.  Back to cited text no. 6
    
7.
ElObeid AS, Kamal-Eldin A, Abdelhalim MAK, Haseeb AM. Pharmacological properties of melanin and its function in health. Basic Clin Pharmacol Toxicol 2017;120:515-22.  Back to cited text no. 7
    
8.
Hamanaka T, Nishizawa K, Sakasegawa Y, Oguma A, Teruya K, Kurahashi H, et al. Melanin or a melanin-like substance interacts with the N-terminal portion of prion protein and inhibits abnormal prion protein formation in prion-infected cells. J Virol 2017;91:e01862-16.  Back to cited text no. 8
    
9.
Dorshorst B, Okimoto R, Ashwell C. Genomic regions associated with dermal hyperpigmentation, polydactyly and other morphological traits in the Silkie chicken. J Hered 2010;101:339-50.  Back to cited text no. 9
    
10.
Zhang H, Ge T, Peng S, Zhong S, Zhou Z. Microstructure features of proventriculus and ultrastructure of the gastric gland cells in Chinese Taihe black-bone silky fowl (Gallus gallus domesticus Brisson). Anat Histol Embryol 2016;45:1-8.  Back to cited text no. 10
    
11.
da Silva RT, Hokoç JN, de Mello FG, Gardino PF. Differential immunodetection of L-DOPA decarboxylase and tyrosine hydroxylase in the vertebrate retina. Int J Dev Neurosci 2009;27:469-76.  Back to cited text no. 11
    
12.
Zecca L, Stroppolo A, Gatti A, Tampellini D, Toscani M, Gallorini M, et al. The role of iron and copper molecules in the neuronal vulnerability of locus coeruleus and substantia nigra during aging. Proc Natl Acad Sci U S A 2004;101:9843-8.  Back to cited text no. 12
    
13.
Kubrusly RC, Panizzutti R, Gardino PF, Stutz B, Reis RA, Ventura AL, et al. Expression of functional dopaminergic phenotype in purified cultured Müller cells from vertebrate retina. Neurochem Int 2008;53:63-70.  Back to cited text no. 13
    
14.
Knörle R. Neuromelanin in Parkinson's disease: From fenton reaction to calcium signaling. Neurotox Res 2018;33:515-22.  Back to cited text no. 14
    
15.
Zeng J, Peng S, Zhong S, Zhang H. The spermatozoal ultrastructure of the Chinese mitten crab (Eriocheir sinensis). J Microsc Ultrastruct 2019;7:181-4.  Back to cited text no. 15
[PUBMED]  [Full text]  
16.
Passos PP, Borba JM, Rocha-de-Melo AP, Guedes RC, da Silva RP, Filho WT, et al. Dopaminergic cell populations of the rat substantia nigra are differentially affected by essential fatty acid dietary restriction over two generations. J Chem Neuroanat 2012;44:66-75.  Back to cited text no. 16
    
17.
Zeng C, Jose PA. Dopamine receptors: Important antihypertensive counterbalance against hypertensive factors. Hypertension 2011;57:11-7.  Back to cited text no. 17
    
18.
Lambert GW, Eisenhofer G, Cox HS, Horne M, Kalff V, Kelly M, et al. Direct determination of homovanillic acid release from the human brain, an indicator of central dopaminergic activity. Life Sci 1991;49:1061-72.  Back to cited text no. 18
    
19.
Zecca L, Costi P, Mecacci C, Ito S, Terreni M, Sonnino S. Interaction of human substantia nigra neuromelanin with lipids and peptides. J Neurochem 2000;74:1758-65.  Back to cited text no. 19
    
20.
Fujii R. The regulation of motile activity in fish chromatophores. Pigment Cell Res 2000;13:300-19.  Back to cited text no. 20
    
21.
Vogliardi S, Allegri G, Bertazzo A, Costa CV, Seraglia R, Traldi P. An investigation on the role of 5-hydroxytryptophan in the biosynthesis of melanins. J Mass Spectrom 2002;37:1292-6.  Back to cited text no. 21
    
22.
Salim S, Ali SA. Vertebrate melanophores as potential model for drug discovery and development: A review. Cell Mol Biol Lett 2011;16:162-200.  Back to cited text no. 22
    
23.
Gillbro JM, Marles LK, Hibberts NA, Schallreuter KU. Autocrine catecholamine biosynthesis and the beta-adrenoceptor signal promote pigmentation in human epidermal melanocytes. J Invest Dermatol 2004;123:346-53.  Back to cited text no. 23
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

  Materials and Me...
  In this article
Abstract
Introduction
Results
Discussion
Conclusion
References
Article Figures

 Article Access Statistics
    Viewed1584    
    Printed100    
    Emailed0    
    PDF Downloaded112    
    Comments [Add]    

Recommend this journal