Cardiac histology (I)
 The structure of the heart undergoes  constant adaptation to physiologic changes in the organism. These changes are  varied and take place from the time of embryonic development to senescence. The  difference between physiological and pathological adaptive mechanisms is  sometimes subtle. Therefore, it is important to understand that the structure  of the heart is modified by a continuum of evolving adaptation of the organ to  the needs of the organism. In many instances, pathologic changes affecting the  heart have a structural substrate, whether they are due to genetic or acquired  processes.  Like any other organ, the  heart has cells that contribute to the formation of the stroma (the connective  tissue scaffold of the organ) and cells that form the parenchyma (the  physiological-working-tissue of the organ, in the case of the heart these are the myocytes). Thus the basic cellular unit of the  parenchyma of the cardiac muscle is the cardiac myocyte. 
    
 This light microscopic image shows normal cardiac myocytes in longitudinal section (accross the screen).  The striations on the myocytes correspond to the sarcomeres (see below and sarcomeres).
 The myocytes are somewhat tubular in shape.  The width of their sarcoplasm (cell cytoplasm) is between 20 and 30 µm.  They display a single centrally located nucleus.  The connective tissue stroma invests the myocytees and the capillary endothelial cells.  The capillaries are present in a 1:1 ratio with the myocytes. 
  
    
From the histologic  standpoint the structure of the cardiac myocyte is best understood if one  integrates the knowledge acquired from the study of the basic molecular  components of this cell type. The cardiac myocyte is a specialized cell  type whose function is to contract. It is striated muscle, which means that  when observed through a microscope, the cells of the heart have a banding  pattern with periodicity across the length of the cell. At first glance the  cardiac myocyte, like any other cell has a cell membrane, which is called the  sarcolemma (sarco = muscle; lemma = membrane). The myocyte also has a  cytoplasm, which is called the sarcoplasm. It also has a nucleus, which is  located in the center of the cell. (Unlike skeletal muscle, in which the  nuclei are located towards the periphery of the cell). These two basic  components, the sarcolemma and the sarcoplasm of the cell are complex  structures that have specialized functions. This image shows typical  cardiac myocytes with striations and central nuclei.
 Higher magnification of  the micrograph below shows the striated pattern, with a central nucleus (Purple) and a nucleolus (Darker Blue/Red) within the nucleus of the myocyte. The striations are formed by the periodicity of the sarcomeres. The sarcomere is the functional contractile unit of the myocyte. It is composed of several distinct structures. It is delimited by two Z bands. The structure of the myocyte is dynamic, and the cell can grow in size on the basis of physiologic or pathologic stimuli. This  growth is called myocyte hypertrophy. In addition, the extracellular matrix supporting the myocytes can also increase, and in pathologic states this is called fibrosis. There are two types of fibrosis in the heart, interstitial fibrosis and replacement fibrosis.
 Higher magnification of  the micrograph below shows the striated pattern, with a central nucleus (Purple) and a nucleolus (Darker Blue/Red) within the nucleus of the myocyte. The striations are formed by the periodicity of the sarcomeres. The sarcomere is the functional contractile unit of the myocyte. It is composed of several distinct structures. It is delimited by two Z bands. The structure of the myocyte is dynamic, and the cell can grow in size on the basis of physiologic or pathologic stimuli. This  growth is called myocyte hypertrophy. In addition, the extracellular matrix supporting the myocytes can also increase, and in pathologic states this is called fibrosis. There are two types of fibrosis in the heart, interstitial fibrosis and replacement fibrosis.
 The Z bands or discs are the dark (electron dense) vertical bands seen in the electron micrograph of a myocyte below. The lighter structure in the center is the nucleus. The round darker gray structures around the nucleus are the mitochondria. Thus, this micrograph shows about 8 rows (from top to bottom) of myofibrils composed of sarcomeres (about 19 sarcomeres across the top of the micrograph). The average length of a relaxed sarcomere is 2µm from one Z band to the next Z band.
The Z bands or discs are the dark (electron dense) vertical bands seen in the electron micrograph of a myocyte below. The lighter structure in the center is the nucleus. The round darker gray structures around the nucleus are the mitochondria. Thus, this micrograph shows about 8 rows (from top to bottom) of myofibrils composed of sarcomeres (about 19 sarcomeres across the top of the micrograph). The average length of a relaxed sarcomere is 2µm from one Z band to the next Z band. 
At higher magnification the detailed structure of the myocyte is shown here. 


