• Nenhum resultado encontrado

Three-dimensional computer modeling of birds proepicardium on different stages of embryogenesis

N/A
N/A
Protected

Academic year: 2016

Share "Three-dimensional computer modeling of birds proepicardium on different stages of embryogenesis"

Copied!
8
0
0

Texto

(1)

.

.

-:

-,

-, .

Н і : 29.01.2009

П я : 20.03.2009

К 611.12:611.013

И - „А

” (

0105U007837).

. ,

-, .

,

; :

,

, ,

-. , ,

,

-, , .

,

. Cobb 500;

, Photoshop

CS2, Amira for microscopy 5.0, 3ds max 8.0,

15, 16, 17, 18, 21 V.Hamburger, H.Hamilton,

1951. 14

20 .

, , ,

.

. 21 27

;

. « »

-.

і . – 2009. – . ІІІ, № 2. – . 47-54.

© . . , 2009

Pototskaya O.Yu. Three-dimensional computer modeling of birds proepicardium on different stages of embryogene-sis.

Summary. As the proepicardium is the source of many cell populations of the mature heart, including cell components of coronary vessels, its investigation became actual last time. It is known, that there are some differences between birds and mammalian proepicardium; one of them consists in the way, in which they contact to myocardium: mammalian proepicar-dium produce vesicles, which contact to atrioventricular groove, wile in birds there is no vesicles and whole protrusions of proepicardium attach to the heart. But, recent years it became evident, that in rat proepicardium there are no vesicles during all stages of its existence, and in birds there is a proepicardium-like structure producing vesicles, which attach to the heart. Thus, the goal of our research was to characterize changes in the shape of proepicardium during bird’s embryogenesis. We used Cobb 500 chick embryos as a material; on the basis of pictures of proepicardium serial sections, with the help of Photo-shop CS2, Amira for microscopy 5.0, 3ds max 8.0 computer programs, we made three-dimensional models of proepicardium on 15, 16, 17, 18, 21 stages of development by V.Hamburger, H.Hamilton, 1951. The most important changes in proepicar-dium shape observed from 14 to 20 stages of development. During this period proepicarproepicar-dium appeared on the right horn of sinus venous, enlarged and formed several crests, which contacted to atrioventricular groove. Coalescence of these crests led to dorsal mesocardium formation. From 21 to 27 stages of development there were no significant changes in proepicardium shape; the area of its contact to sinus venous was grown downwards while the area of contact to the heart enlarged. No vesi-cles, no “finger-like protrusions” were observed on any stage of bird’s development.

(2)

__________________________________________________________________________________ І • 2009 • ІІI • №2

48 ( ) -, , ; ,

(Lie-Venema . et

al., 2005). «

-» -. , , ( ). 13-14 V.Hamburger, H.Hamilton (1951) ( )

( К).

,

(Winter E.M., Gittenberger-de Groot A.C., 2007; Schulte I. et al., 2007). 15-16

-,

(Schulte I. et al., 2007; Nachirnei P. . et al., 2003).

P. .Nachirnei (2003)

-,

-,

-,

-.

17-18

К,

. 18

-

.

26 ;

-,

(Lie-Venema . et al.,

2005). -: , « » .

-L.S.Rodgers (2008)

-, -. , - , , -, . , -, , , , -, , . -,

-. , T.Nesbitt c

(2006) ,

-, . -, -. , (

. ., 2008).

-

-.

Cobb 500;

39,4º ,

80%.

8 .

V.Hamburger, H.Hamilton, (1951) B.J.Martinsen (2005).

,

,

-, .

5 (

)

,

, .

Photoshop

CS2 ( ), Amira for

microscopy 5.0 (

-), 3ds max 8.0 (

).

-І. . (2007).

14

/

;

( . 1), ,

. , -. 15 ; , ( –

. 2 , ) ,

(3)

-,

( .

2 , ).

. 1. Э э 14

. ×100; ×400. э

-. я я я ч . –

-ч я .

16

-,

( . 2 , ),

«

-».

( . 2 , ).

К ( . 2 , ).

,

-.

17

-;

,

( . 3 , ).

( . 3 , ),

. 16

.

18

. ,

,

;

( . 3 , ).

,

-,

-( . 3 ).

--

-- .

19 21

. . «

-»,

26-27 .

( . 4 , ). ,

,

,

( . 4 ).

-,

-, ,

.

, .

,

-,

, -

-.

( . 4 ).

,

,

-,

( . 4, ).

14

,

(Nachirnei P. . et al., 2003). 20-21 (

(4)

__________________________________________________________________________________ І • 2009 • ІІI • №2

50

50 мкм 50 мкм

. 2. Э э - – 15, - – 16 . , ×100; , ×400. .

я я я ч ы ; я я я ч ы . , , , – ы Э,

(5)

50 мкм

50 мкм 50 мкм

. 3. Э э - – 17, - – 18 . , ×100; , ×400. ы

( , ), ( , ). я я я ч ы ; я я я ч ы

. , , , – ы Э, , , . , – ;

(6)

__________________________________________________________________________________ І • 2009 • ІІI • №2

52

50 мкм

. 4. Э э - –

21, - – 24 . , ×100; ,

×400. э ( ,

); ы

( , ). я я я ч ы

; я я я ч ы . ,

– ы Э,

(7)

« -» (Nesbitt T. et al., 2006; Winter E.M., Gittenberger-de Groot A.C., 2007;

Schulte I. et al., 2007), ,

-,

,

( . 3 , , , ). ,

(

)

-,

-, , ,

-.

20

-, , , , -. -, , ,

(Winter E.M., Gittenberger-de Groot A.C., 2007).

,

-. ,

-,

18 .

(

.4 ), ,

-,

(Ratajska A. et al., 2006).

14 27

-.

14 20 ,

,

,

-. 21 26-27

; . -. ; -.

І. .

'є '

/ І. . //

-. – 2007-. – -. 1, № 1. – . 135-139.

. .

: / . .

// . – 2008. – . 2, № 4. – . 37-43.

Differential growth and multicellular villi direct proepicardial translocation to the developing mouse heart / Laurel S. Rodgers, Sofia Lalani, Ray B.

Run-yan, Todd D. Camenisch // Dev. Dyn. – 2008. – Vol.

237. – P. 145–152.

Epicardial development in the rat: a new per-spective / Tresa Nesbitt, Aubrey Lemley, Jeff Davis [et al.] // Microsc. Microanal. – 2006. – Vol. 12. – P. 390–398.

Hamburger V. A series of normal stages in the development of the chick embryo / Viktor Ham-burger, Howard L. Hamilton // J. Morphol. – 1951. - Vol. 88, № 1. – . 49-92.

Martinsen B. J. Reference guide to the stages of chick heart embryology / Brad J. Martinsen // Dev. Dyn. – 2005. – Vol. 233. – P. 1217–1237.

Morphological and molecular left-right

asym-metries in the development of the proepicardium: a comparative analysis on mouse and chick embryos / Inga Schulte, Jan Schlueter, Radwan Abu-Issa [et al.] // Anat. Embryol. (Berl). – 2007. – Vol. 176, № 2. – P. 9-183.

Myocardial heterogeneity in permissiveness for epicardium-derived cells and endothelial precursor cells along the developing heart tube at the onset of coronary vascularization / Heleen Lie-Venema,

Is-mail Eralp, Saskia Maas [et al.] // Anat. Rec. – 2005.

– Vol. 282A. – P. 120–129.

Nahirney P. C. Evidence for an extracellular matrix bridge guiding proepicardial cell migration to the myocardium of chick embryos / Patrick C. Nahirney, Takashi Mikawa, Donald A. Fischman // Dev. Dyn. – 2003. – Vol. 227. – P. 511-523.

Vasculogenesis of the embryonic heart: origin of blood island-like structures / Anna Ratajska, Elz-bieta Czarnowska, Agnieszka Kołodzinska [et al.] // Anat. Rec. – 2006. – Vol. 288A. – P. 223–232.

(8)

__________________________________________________________________________________ І • 2009 • ІІI • №2

54

. . і ' і і

.

. , є

,

. , ;

є : є ,

є , , ,

є . , ,

є ,

, є , є . ,

.

Cobb 500; ,

-’ Photoshop CS2, Amira for microscopy 5.0, 3ds max 8.0,

15, 16, 17, 18, 21 V.Hamburger, H.Hamilton, 1951.

14 20 .

’ , ,

.

. 21 27 ;

, .

« » .

Referências

Documentos relacionados

There were no significant differences between treatments in the growth, quality or composition of the femur or tibia of the birds, showing that the use of calcium anacardate as a

Surprisingly, one of them is the definition of Fractional Differintegration (FD). In fact, there are several definitions that lead to different results

Knowledge in diet is essential to development of hypothesis to elucidate the evolution of the coexistence between species, but studies about diet of birds is still scarce and

The reason why the blockade of one vasodilator com- pensates for the actions of the other is not known, nor is it known why there are circumstances in which the inhibition of NO or

EPCs: endothelial progenitor cells; NICD: Notch intracellular domain; Wnts: Wnt signaling; MSCs: mesenchymal stromal cells; CPCs: cardiac progenitor cells; RBP-J k :

neurons do project to the spinal cord in birds reinforces the view that the mammalian mid- brain may contain separate populations of neurons as well - UCN+ neurons projecting to

This result shows that birds of the Pescoço Pelado lineage tend to have the greatest weight in adulthood, and the birds of the Pesadão lineage, which presented lower values

The aim of this study is to determine whether, considering the Hymenoptera and birds vision spectrum, there are differences in color of spiders, egg sacs and branches. where