Struktur Histologi Sistem Reproduksi Pria (Kuliah Histologi)-Genital Duct, Accesory Gland dan Penis

 Spermatozoa setelah diproduksi di Tubulus Semiferus akan di transport secara pasif, karena belum memiliki kemampuan untuk bergerak. Saluran untuk transportasi spermatozoa secara keseluruhan disebut dengan Genital Duct. Genital duct ada yang berlokasi di dalam testis sehingga disebut intratestitular dan ada yang berada diluar testis disebut extratestistular. Yang termasuk intratestiscular adalah Tubuli Recti, dan Rete Testis. Beberapa buku juga memasukan Ductus efferent sebagai ductus intratestiscular dan ada juga yang menyebutkan sebagai extra testicular. Saluran extra testiscular selanjutnya adalah Epididimis, Ductus/ Vas Deferen, Ductus Ejaculatorius dan selanjutnya Uretra. Genital duct memiliki struktur histologi dan lapisan yang bervariasi sesuai dengan fungsinya. 

Ada tiga kelenjar yang memperoduksi cairan yang membentuk semen atau mani, yaitu kelenjar Vesicula Seminalis, Kelenjar Prostat dan Kelenjar Bulbourethral. Semen adalah campuran antara spermatozoa (sel) dengan cairan produk dari kelenjar ini. Saat seorang pria ejakulasi , volume semen yang keluar paling sedikit  2 mili liter dan sebagian besar merupakan produk dari Kelenjar Vesicula Seminalis. Prosuk Kelenjar Vescula seminalis kaya denganfruktosa untuk memberi nutrisi pada spermatozoa. Kelanjar prostat berada tepat dibawah kandung kemih (vesica urinaria) dan ditembus oleh uretra. Kelenjar prostat mengeluarkan produknya langsung ke uretra, produknya kaya dengan beberapa enzim. Pada usia lansia sering terjadi pembesaran prostat sehingga menghambat pengeluaran urin/kencing yang disebut dengan BPH. Kelenjar bulbouretral paling kecil diantara ketiganya, lokasinya di pangkal penis dan memproduksi cairan mukus untuk membersihkan uretra sebelum ejakuasi

Penis merupakan organ kopulasi pria, disusun oleh tiga tabung yaitu dua corpus cavernosum dibagian dorsal dan satu corpus spongiosum dibagian ventral. Keiga tagung ini dibungkus oleh jaringan ikat Tunika Albugenia. Saat penis ereksi darah dipompa kedalam corpus cavernosum, dan darah akan kembali keluar setelah ejakulasi.

Kulaih selengkapnya bisa dilihat pada video dibawah ini

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Posted in ejakulasi , epididimis , ereksi , genital duct , histologi , kelenjar prostat , kelenjar vesikula seminalis , kuliah histologi , mani , penis , reproduksi pria , tubulus seminiferus , uretra , vas deferen

Struktur Histologi Sistem Reproduksi Pria (Kuliah Histologi)- Testis dan Spermatogenesis

Testis berada dalam kantung yang disebut dengan Scrotum, yang berperan penting dalam fisiologi Testis agar proses spermatogenesis bisa berlangsung dengan baik. Testis pada bagian luarnya dilapisi oleh Tunika Albugenia. Testis dibagi-bagi menjadi ruang-ruang kecil yang disebut Lobuli Testis. Di dalam Lobuli Testis diisi oleh Tubulus Seminiferus. Tubulus Seminiferus merupakan tempat proses spermatogenesis, struktur ini dilapisi oleh Sel Sertoli dan sel-sel spermatogenik. Sel sertoli sangat penting perannya dalam melindungi sel-sel spermatogenik dengan membentuk struktur Blood-Testis Barrier. Saat seorang pria lahir hanya memliki sel spermatogenik spermatogenia, setelah pubertas akan muncul jenis sel-sel baru yaitu spermatosit primer, spermatosist sekunder dan spermatid. Munculnya jenis sel-sel ini karena proses spermatohgenenis, dimana terjadi pembelahan sel yaitu mitosis, meiosis dan ada proses diferensiasi. Diantara tunulus seminiferus, yaitu pada parenkim testis ada sel Leydig yang berperan dalams mensintesis Testosteron. Testosteron berperan dalam mengatur spermatogenesis dan memberikan ciri seks sekunder pada pria.

Kuliah selengkapnya bisa di lihat pada video dibawah ini 

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Posted in blood-tests barrier , histologi , kuliah histologi , reproduksi pria , sel leydig , spermatid , spermatogenesis , spermatogonia , spermatosit , spermiogenesis , testis , tubulus seminiferus

Struktur Histologi Sistem Reproduksi Pria (Kuliah Histologi)- Pengantar

Sistem reproduksi pria secara anatomi terdiri dari Testis , Genital Duct, Asesori Gland dan Penis. Testis  merupakan tempat produksi spermatozoa dan juga tempat sintesis hormon Testosteeron. Spermatozoa setelah diproduksi melalui prses spermatogenesis di Tubulus Semiferous kemudian akan ditansport untuk disimpan dan dimaturasi di Epididimis. Sebelum sampai di Epididmis spermatozoa harus melewati beberapa saluran, yaitu Tubuli Recti dan Rete Testis. Didalam Epidimis disimpan dan dimatangkan atau dimaturasi, spermatozoa bisa tinggal dalam waktu yang cukup lama di organ ini. Juka ada aktivitas seksual maka spermatozoa akan ditarnsport ke saluran berikutnya yaitu Duktus Deferen atau Vas Diferen , sesampai di duktus ejakulatorius spermatozoa akan dicampur dengan cairan yang diproduksi oleh asesori gland yaitu Vesikula Seminalis dan Kelenjar Prostat. Spermatozoa yang sudah dicampus dengan produk dari asesori gland disebut dengan semen, yang kemudian akan dikeluarkan melalalui organ Penis, prosesnya disebut ejakulasi. Ada asesori gland lain yang disebut Bulbourethtal Gland yang berberan dalam membersihkan /melubrikasi uretra. Informasi lengkap tentang pengantar Histologi Sistem Reproduksi Pria Bisa di lihat pada Video di bawah ini : 

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Posted in genital duct , histologi , kelenjar prostat , kelenjar vesikula seminalis , kuliah histologi , penis , pria , rete testis , spermatozoa , testis , tubuli recti , vas deferen , video histologi

Pengantar Praktikum Histology Male and Female Genital System 26 Juni 2015

Kepada mahasiswa Fakultas Kedokteran Universitas Udayana yang sedang mengikuti Blok The Reproductive System and Disorders diharapkan untuk membaca pengantar praktikum histology sebelum mengikuti praktikum pada hari Jumat tanggal 26 Juni 2015.

Pengantar praktikum histology bisa dibaca pada alamat/ link ini :

• PENGANTAR PRAKTIKUM MALE HISTOLOGY
• PENGANTAR PRAKTIKUM FEMALE HISTOLOGY

JIka Anda ingin versi PDF bisa didownload di alamat ini :

• PENGANTAR PRAKTIKUM MALE HISTOLOGY (PDF)

• PENGANTAR PRAKTIKUM FEMALE HISTOLOGY

Diharapkan juga untuk kembali membaca teks book histologi, sebelum praktikum agar pemahaman tentang struktur histologis male and female reproductive system menjadi lebih baik.

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Posted in 2015 , histologi , praktikum , reproductive system

Student Project-Struktur Mikroskopis Kelenjar Saliva dan Perannya dalam Menjaga Kesehatan Rongga Mulut

Student Project mahasiswa PSPDG FK UNUD pada blok Basic Dentistry, Makalah ini tentang struktur mikroskopis kelenjar saliva (parotis, submandibularis dan sublingualis) dan peranannya dalam menjaga kesehatan (sistem pertahanan) rongga mulut STUDENT PROJECT PSPDG 2014-kelenjar saliva dan perannya dalam sistem pertahanan rongga mulut.pdf

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Posted in fkunud , kelenjar , pspdg , rongga mulut , saliva , student project

Student Project - Struktur Mikroskopis Tonsil dan Perannya dalam Sistem Pertahanan Rongga Mulut

Student Project mahasiswa PSPDG FK UNUD pada blok Basic Dentistry, Makalah ini tentang struktur mikroskopis tonsil (tonsila palatina, lingualis, dan faringeal) dan peranannya dalam sistem pertahanan rongga mulut terhadap patogen



Student Project Blok Basic Denstistry PSPDG FK UNUD -Tonsil.pdf

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Posted in 2014 , basic dentistry , immune system , oral cavity , pspdg , rongga mulut , student project , tonsil

Basic Tissue /Jaringan Dasar-Powerpoint

Presentasi ini tentang empat jaringan dasar yaitu : jaringan ikat, otot, saraf dan epitel yang menyusun semua organ pada tubuh manusia. Memahami pengertian, struktur serta karakteristik empat jaringan dasar sangat penting dalam rangka memahami struktur mikroskopis organ tubuh, karena semua organ tubuh manusia disusun oleh kombinasi dari empat jaringan dasar ini.


Powerpoint ini dipresentasikan pada tanggal 15 Oktober 2014 untuk mahasiswa PSPDG FK UNUD .

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Posted in 2014 , fkunud , jaringan dasar , power point , pspdg

Belajar Mandiri (Independent Learning) Untuk Mahasiswa

Presentasi ini disampaikan pada kuliah studium generale Program Studi Fisioterapi Fakultas Kedokteran Universitas Udayana pada tanggal 5 September 2014. Materi ini penting bagi semua mahasiswa baru karena cara belajar di Universitas sangat berbeda dari cara belajar di sekolah.

Cara belajar di Universitas menganut metode belajar mandiri (independent learning), pada metode ini lebih menekankan pada BELAJAR bukan MENGAJAR. Dosen lebih berperan sebagi fasilitator dan menciptakan suasana belajar, dan mahasiswa dituntuk untuk mencari ilmu secara mandiri. 

Belajar mandiri memberikan banyak keuntungan bagi mahasiswa baik dalam proses pembelajaran maupun dalam menjalami profesinya. 

Pada presentasi ini akan dijelaskan  tentang definisi belajar mandiri/Independent Learning, karakteristik belajar mandiri, peran guru/dosen dalam belajar mandiri, bagaimana cara menjadi independent learner (pelajar yang mandiri), peran pelajar/mahasiswa dan guru/dosen dalam belajar mandiri, dan peran study Guide dalam independent learning tentang difinisi 

Selamat menyimak, semoga bermanfaat...

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Posted in 2014 , belajar , fisioterapi , power point

Pengantar Praktikum Histology : Male and Female Reproductive System

Kepada mahasiswa Fakultas Kedokteran Universitas Udayana semester VI yang sedang mengikuti Blok The Reproductive System and Disorders diharapkan untuk membaca pengantar praktikum histology sebelum mengikuti praktikum pada hari Jumat tanggal 19 Juli 2013.

Pengantar praktikum histology bisa dibaca pada alamat/ link ini :

• PENGANTAR PRAKTIKUM MALE HISTOLOGY
• PENGANTAR PRAKTIKUM FEMALE HISTOLOGY

JIka Anda ingin versi PDF bisa didownload di alamat ini :

• PENGANTAR PRAKTIKUM MALE HISTOLOGY (PDF)

• PENGANTAR PRAKTIKUM FEMALE HISTOLOGY

Diharapkan juga untuk kembali membaca teks book histologi, sebelum praktikum agar pemahaman tentang struktur histologis male and female reproductive system menjadi lebih baik.

Read More [...]

Posted in 2013 , histologi , praktikum , reproductive system

Cerebro Spinal Fluid Production and Circulation (Animation)

Animasi ini menjelaskan tentang fungsi cerebrospinal fluid (CSF), tempat produksi CSF, Aliran CSF dari ventrikel sampai ke subarachnoid space, ke central canal medulla spinalis dan akhirnya diabsorbsi kembali ke vena. Animasi ini sangat membantu untuk memahami produksi dan fungsi CSF.

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Posted in animation , blok neuroscience , brain , cerebrospinal fluid , ependymal cell , neuroscience , video

Blood-Brain Barrier Animation

Pada video/animasi ini ditampilkan struktur Blood-Brain Barrier yang terutama disusun oleh tight-junction dari endothel, dan dukung oleh Astrosit. Dijelaskan juga beberapa masalah yang dihadapi jika ingin memasukan obat kedalam jaringan otak. Dan saat ini para ahli sedang mengembangkan metode untuk dapat memasukan obat kedalam jaringan otak. Semoga video ini bisa membantu Anda dalam memahami Blood-Brain Barrier. Selamat Belajar

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Posted in animation , blok neuroscience , blood , blood-barin barrier , brain , neuroscience , video

Degeneration & Regeneration of Nerve Tissue-Histology of Nervous System

Mammalian neurons usually do not divide, and their degeneration represents a permanent loss. Peripheral nerve fibers can regenerate if their perikaryons are not destroyed.

In contrast to nerve cells, neuroglia of the central nervous system—and Schwann cells and ganglionic satellite cells of the peripheral nervous system—are able to divide by mitosis. Spaces in the central nervous system left by nerve cells lost by disease or injury are invaded by neuroglia.

Because nerves are widely distributed throughout the body, they are often injured. When a nerve axon is transected, degenerative changes take place, followed by a reparative phase.

In a wounded nerve fiber, it is important to distinguish the changes occurring in the proximal segment from those in the distal segment. The proximal segment maintains its continuity with the trophic center (perikaryon) and frequently regenerates. The distal segment, separated from the nerve cell body, degenerates.

Axonal injury causes several changes in the perikaryon: chromatolysis, ie, dissolution of Nissl substances with a consequent decrease in cytoplasmic basophilia; an increase in the volume of the perikaryon; and migration of the nucleus to a peripheral position in the perikaryon.

In the nerve stub distal to the injury, both the axon and the myelin sheath degenerate completely, and their remnants, excluding their connective tissue and perineurial sheaths, are removed by macrophages. While these regressive changes take place, Schwann cells proliferate within the remaining connective tissue sleeve, giving rise to solid cellular columns. These rows of Schwann cells serve as guides to the sprouting axons formed during the reparative phase.

After the regressive changes, the proximal segment of the axon grows and branches, forming several filaments that progress in the direction of the columns of Schwann cells. Only fibers that penetrate these Schwann cell columns will continue to grow and reach an effector organ.

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Choroid Plexus & Cerebrospinal Fluid-Histology of Nervous System

The choroid plexus consists of invaginated folds of pia mater, rich in dilated fenestrated capillaries, that penetrate the interior of the brain ventricles. It is found in the roofs of the third and fourth ventricles and in part in the walls of the lateral ventricles.

The choroid plexus is composed of loose connective tissue of the pia mater, covered by a simple cuboidal or low columnar epithelium made of ion-transporting cells .

The main function of the choroid plexus is to elaborate cerebrospinal fluid, which contains only a small amount of solids and completely fills the ventricles, central canal of the spinal cord, subarachnoid space, and perivascular space. Cerebrospinal fluid is important for the metabolism of the central nervous system and acts as a protective device against mechanical shocks.

Cerebrospinal fluid is clear, has a low density (1.004–1.008 g/ mL), and is very low in protein content. A few desquamated cells and two to five lymphocytes per milliliter are also present. Cerebrospinal fluid is continuously produced and circulates through the ventricles, from which it passes into the subarachnoid space. There, arachnoid villi provide the main pathway for absorption of cerebrospinal fluid into the venous circulation.

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The Blood-Brain Barrier-Histology of Nervous System

The blood–brain barrier is a functional barrier that prevents the passage of some substances, such as antibiotics and chemical and bacterial toxic matter, from the blood to nerve tissue.

The blood–brain barrier results from the reduced permeability that is characteristic of blood capillaries of nerve tissue. Occluding junctions, which provide continuity between the endothelial cells of these capillaries, represent the main structural component of the barrier. The cytoplasm of these endothelial cells does not have the fenestrations found in many other locations, and very few pinocytotic vesicles are observed. The expansions of neuroglial cell processes that envelop the capillaries (astrocytes) are partly responsible for their low permeability.

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Meninges-Histology of Nervous System

The skull and the vertebral column protect the central nervous system. It is also encased in membranes of connective tissue called the meninges . Starting with the outermost layer, the meninges are the dura mater, arachnoid, and pia mater. The arachnoid and the pia mater are linked together and are often considered a single membrane called the pia-arachnoid.

Dura Mater

The dura mater is the external layer and is composed of dense connective tissue continuous with the periosteum of the skull. The dura mater that envelops the spinal cord is separated from the periosteum of the vertebrae by the epidural space, which contains thin-walled veins, loose connective tissue, and adipose tissue. The dura mater is always separated from the arachnoid by the thin subdural space.

Arachnoid

The arachnoid has two components: a layer in contact with the dura mater and a system of trabeculae connecting the layer with the pia mater. The cavities between the trabeculae form the subarachnoid space, which is filled with cerebrospinal fluid and is completely separated from the subdural space. This space forms a hydraulic cushion that protects the central nervous system from trauma. The subarachnoid space communicates with the ventricles of the brain. The arachnoid is composed of connective tissue devoid of blood vessels. In some areas, the arachnoid perforates the dura mater, forming protrusions that terminate in venous sinuses in the dura mater. These protrusions, which are covered by endothelial cells of the veins, are called arachnoid villi. Their function is to reabsorb cerebrospinal fluid into the blood of the venous sinuses.

Pia Mater

The pia mater is a loose connective tissue containing many blood vessels. Although it is located quite close to the nerve tissue, it is not in contact with nerve cells or fibers. Between the pia mater and the neural elements is a thin layer of neuroglial processes, adhering firmly to the pia mater and forming a physical barrier at the periphery of the central nervous system. This barrier separates the central nervous system from the cerebrospinal fluid. The pia mater follows all the irregularities of the surface of the central nervous system and penetrates it to some extent along with the blood vessels. Squamous cells of mesenchymal origin cover pia mater. Blood vessels penetrate the central nervous system through tunnels covered by pia mater—the perivascular spaces. The pia mater disappears before the blood vessels are transformed into capillaries. In the central nervous system, the blood capillaries are completely covered by expansions of the neuroglial cell processes.

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The Ganglia-Histology of Nervous System

Ganglia are ovoid structures containing neuronal cell bodies and glial cells supported by connective tissue. Because they serve as relay stations to transmit nerve impulses, one nerve enters and another exits from each ganglion. The direction of the nerve impulse determines whether the ganglion will be a sensory or an autonomic ganglion.

Sensory Ganglia

Sensory ganglia receive afferent impulses that go to the central nervous system. Two types of sensory ganglia exist. Some are associated with cranial nerves (cranial ganglia); others are associated with the dorsal root of the spinal nerves and are called spinal ganglia. A connective tissue framework and capsule support the ganglion cells. The neurons of these ganglia are pseudounipolar and relay information from the ganglion's nerve endings to the gray matter of the spinal cord via synapses with local neurons.

 

Autonomic Ganglia

Autonomic ganglia appear as bulbous dilatations in autonomic nerves. Some are located within certain organs, especially in the walls of the digestive tract, where they constitute the intramural ganglia. These ganglia are devoid of connective tissue capsules, and their cells are supported by the stroma of the organ in which they are found. Autonomic ganglia usually have multipolar neurons. As with craniospinal ganglia, autonomic ganglia have neuronal perikaryons with fine Nissl bodies.A layer of satellite cells frequently envelops the neurons of autonomic ganglia. In intramural ganglia, only a few satellite cells are seen around each neuron.

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The Nerves-Histology of Nervous System

In the peripheral nervous system, the nerve fibers are grouped in bundles to form the nerves. Except for a few very thin nerves made up of unmyelinated fibers, nerves have a whitish, homogeneous, glistening appearance because of their myelin and collagen content.

Nerves have an external fibrous coat of dense connective tissue called epineurium, which also fills the space between the bundles of nerve fibers. Each bundle is surrounded by the perineurium, a sleeve formed by layers of flattened epitheliumlike cells. The cells of each layer of the perineurial sleeve are joined at their edges by tight junctions, an arrangement that makes the perineurium a barrier to the passage of most macromolecules and has the important function of protecting the nerve fibers from aggression. Within the perineurial sheath run the Schwann cell-sheathed axons and their enveloping connective tissue, the endoneurium. The endoneurium consists of a thin layer of reticular fibers, produced by Schwann cells.

The nerves establish communication between brain and spinal cord centers and the sense organs and effectors (muscles, glands, etc). They possess afferent and efferent fibers to and from the central nervous system. Afferent fibers carry the information obtained from the interior of the body and the environment to the central nervous system. Efferent fibers carry impulses from the central nervous system to the effector organs commanded by these centers. Nerves possessing only sensory fibers are called sensory nerves; those composed only of fibers carrying impulses to the effectors are called motor nerves. Most nerves have both sensory and motor fibers and are called mixed nerves; these nerves have both myelinated and unmyelinated axons .

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Peripheral Nervous System-Histology of Nervous System

The main components of the peripheral nervous system are the nerves, ganglia, and nerve endings. Nerves are bundles of nerve fibers surrounded by connective tissue sheaths.

Nerve Fibers

Nerve fibers consist of axons enveloped by a special sheath derived from cells of ectodermal origin. Groups of nerve fibers constitute the tracts of the brain, spinal cord, and peripheral nerves.

Myelinated Fibers

In myelinated fibers of the peripheral nervous system, the plasmalemma of the covering Schwann cell winds and wraps around the axon . The layers of membranes of the sheath cell unite and form myelin. Myelin consists of many layers of modified cell membranes. These membranes have a higher proportion of lipids than do other cell membranes. The myelin sheath shows gaps along its path called the nodes of Ranvier; these represent the spaces between adjacent Schwann cells along the length of the axon. Interdigitating processes of Schwann cells partially cover the node. The distance between two nodes is called an internode and consists of one Schwann cell. The length of the internode varies between 1 and 2 mm. There are no Schwann cells in the central nervous system; there, the processes of the oligodendrocytes form the myelin sheath. Oligodendrocytes differ from Schwann cells in that different branches of one cell can envelop segments of several axons .

Unmyelinated Fibers

In both the central and peripheral nervous systems, not all axons are sheathed in myelin. In the peripheral system, all unmyelinated axons are enveloped within simple clefts of the Schwann cells. Unlike their association with individual myelinated axons, each Schwann cell can sheathe many unmyelinated axons. Unmyelinated nerve fibers do not have nodes of Ranvier, because abutting Schwann cells are united to form a continuous sheath.

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The Central Nervous System-Histology of Nervous System

The central nervous system consists of the cerebrum, cerebellum, and spinal cord. It has almost no connective tissue and is therefore a relatively soft, gel-like organ.

When sectioned, the cerebrum, cerebellum, and spinal cord show regions that are white (white matter) and that are gray (gray matter). The differential distribution of myelin in the central nervous system is responsible for these differences: The main component of white matter is myelinated axons and the myelin-producing oligodendrocytes. White matter does not contain neuronal cell bodies.

Gray matter contains neuronal cell bodies, dendrites, and the initial unmyelinated portions of axons and glial cells. This is the region at which synapses occur. Gray matter is prevalent at the surface of the cerebrum and cerebellum, forming the cerebral and cerebellar cortex , whereas white matter is present in more central regions. Aggregates of neuronal cell bodies forming islands of gray matter embedded in the white matter are called nuclei.

In the cerebral cortex, the gray matter has six layers of cells with different forms and sizes. Neurons of some regions of the cerebral cortex register afferent (sensory) impulses; in other regions, efferent (motor) neurons generate motor impulses that control voluntary movements. Cells of the cerebral cortex are related to the integration of sensory information and the initiation of voluntary motor responses.

The cerebellar cortex has three layers : an outer molecular layer, a central layer of large Purkinje cells, and an inner granule layer. The Purkinje cells have a conspicuous cell body and their dendrites are highly developed, assuming the aspect of a fan. These dendrites occupy most of the molecular layer and are the reason for the sparseness of nuclei. The granule layer is formed by very small neurons (the smallest in the body), which are compactly disposed, in contrast to the less cell-dense molecular layer .

In cross sections of the spinal cord, white matter is peripheral and gray matter is central, assuming the shape of an H. In the horizontal bar of this H is an opening, the central canal, which is a remnant of the lumen of the embryonic neural tube. It is lined with ependymal cells. The gray matter of the legs of the H forms the anterior horns. These contain motor neurons whose axons make up the ventral roots of the spinal nerves. Gray matter also forms the posterior horns (the arms of the H), which receive sensory fibers from neurons in the spinal ganglia (dorsal roots).

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Neuroglial Cells-Histology of Nervous System

Glial cells are 10 times more abundant in the mammalian brain than neurons; they surround both cell bodies and their axonal and dendritic processes that occupy the interneuronal spaces.

Nerve tissue has only a very small amount of extracellular matrix, and glial cells furnish a microenvironment suitable for neuronal activity.

1. Oligodendrocytes produce the myelin sheath that provides the electrical insulation of neurons in the central nervous system. These cells have processes that wrap around axons, producing a myelin sheath
2. Schwann cells have the same function as oligodendrocytes but are located around axons in the peripheral nervous system. One Schwann cell forms myelin around a segment of one axon, in contrast to the ability of oligodendrocytes to branch and serve more than one neuron and its processes.
3. Astrocytes are star-shaped cells with multiple radiating processes. Astrocytes bind neurons to capillaries and to the pia mater (a thin connective tissue that covers the central nervous system). Astrocytes with few long processes are called fibrous astrocytes and are located in the white matter; protoplasmic astrocytes, with many short-branched processes, are found in the gray matter. In addition to their supporting function, astrocytes participate in controlling the ionic and chemical environment of neurons. Some astrocytes develop processes with expanded end feet that are linked to endothelial cells. It is believed that through the end feet, astrocytes transfer molecules and ions from the blood to the neurons (Blood-Brain Barrier). Expanded processes are also present at the external surface of the central nervous system, where they make a continuous layer. Furthermore, when the central nervous system is damaged, astrocytes proliferate to form cellular scar tissue. Astrocytes can influence neuronal survival and activity through their ability to regulate constituents of the extracellular environment, absorb local excess of neurotransmitters, and release metabolic and neuroactive molecules. The latter molecules include peptides of the angiotensinogen family, vasoactive endothelins, opioid precursors called enkephalins, and the potentially neurotrophic somatostatin. On the other hand, there is some evidence that astrocytes transport energy-rich compounds from the blood to the neurons and also metabolize glucose to lactate, which is then supplied to the neurons.
4. Ependymal cells are low columnar epithelial cells lining the ventricles of the brain and central canal of the spinal cord. In some locations, ependymal cells are ciliated, which facilitates the movement of cerebrospinal fluid.
5. Microglia are small elongated cells with short irregular processes. Microglia, phagocytic cells that represent the mononuclear phagocytic system in nerve tissue, are derived from precursor cells in the bone marrow. They are involved with inflammation and repair in the adult central nervous system, and they produce and release neutral proteases and oxidative radicals. When activated, microglia retract their processes and assume the morphological characteristics of macrophages, becoming phagocytic and acting as antigen-presenting cells. Microglia secrete a number of immunoregulatory cytokines and dispose of unwanted cellular debris caused by central nervous system lesions.

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