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Comparison of Hematopoietic and Spermatogonial Stem Cell Niches from the Regenerative Medicine Aspect

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Book cover Cell Biology and Translational Medicine, Volume 3

Part of the book series: Advances in Experimental Medicine and Biology ((CBTMED,volume 1107))

Abstract

Recent advances require a dual evaluation of germ and somatic stem cell niches with a regenerative medicine perspective. For a better point of view of the niche concept, it is needed to compare the microenvironments of those niches in respect to several components. The cellular environment of spermatogonial stem cells’ niche consists of Sertoli cells, Leydig cells, vascular endothelial cells, epididymal fat cells, peritubular myoid cells while hematopoietic stem cells have mesenchymal stem cells, osteoblasts, osteoclasts, megacaryocytes, macrophages, vascular endothelial cells, pericytes and adipocytes in their microenvironment. Not only those cells’, but also the effect of the other factors such as hormones, growth factors, chemokines, cytokines, extracellular matrix components, biomechanical forces (like shear stress, tension or compression) and physical environmental elements such as temperature, oxygen level and pH will be clarified during the chapter. Because it is known that the microenvironment has an important role in the stem cell homeostasis and disease conditions, it is crucial to understand the details of the microenvironment and to be able to compare the niche concepts of the different types of stem cells from each other, for the regenerative interventions. Indeed, the purpose of this chapter is to point out the usage of niche engineering within the further studies in the regenerative medicine field. Decellularized, synthetic or non-synthetic scaffolds may help to mimic the stem cell niche. However, the shared or different characteristics of germ and somatic stem cell microenvironments are necessary to constitute a proper niche model. When considered from this aspect, it is possible to produce some strategies on the personalized medicine by using those artificial models of stem cell microenvironment.

The original data that is presented in this work is supported by Technical and Research Council of Turkey (TUBITAK, # 113S819) and, Hacettepe University Research Fund (# THD-2017-13430, # 013D04101005) grants. The authors do not have any financial disclosure.

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Abbreviations

2-AG:

2 arachidonoyl glycerol

ABP:

Androgen Binding Protein

ADAM:

A Disintegrin and Metalloprotease

AEA:

(anandamide), N-arachidonoyl ethanolamine

AGM:

Aorta-Gonad-Mesonephros

BADGE:

Bisphenol A Diglycidyl Ether

bFGF:

Basic Fibroblast Growth Factor

BMP:

Bone Morphogenetic Protein

BTB:

Blood Testis Barrier

CB1 :

Cannabinoid receptor targets type-1

CB2:

Cannabinoid receptor targets type-2

CLEC-2:

C-type lectin-like receptor-2

CNS:

Central Nervous System

CSF1:

Colony Stimulating factor 1

CSFR1:

CSF1 Receptor

CXCL12:

Chemokine (C-X-C motif) ligand 12

CXCR4:

Chemokine receptor type 4

EC:

Endothelial Cell

ECM:

Extracellular Matrix

ECS:

Endocannabinoids

ES:

Ectoplazmic

EWAT:

Epididymal White Adipose Tissue

FAAH:

Fatty Acid Amide hydrolase

FGF:

Fibroblast Growth Factor

FGFR2:

FGF Receptor 2

FSH:

Follicle-Stimulating Hormone

G-CSF:

Granulocyte Colony-Stimulating Factor

GDNF:

Glial cell-line Derived Neutrophic Factor

GFRA1:

GDNF-Family Receptor α1

GPCR:

G Protein-Coupled Receptors

hCG:

Human Chorionic Gonadotropin

HSC:

Hematopoietic Stem Cells

HSPC:

Hematopoietic Stem/Progenitor Cells

IM:

Interstitial Macrophage

KDR:

Kinase Insert Domain Receptor

LC:

Leydig Cell

LH:

Luteinizing Hormone

MAGL:

Monoacylglycerol lipase

MAPK:

Mitogen-Activated Protein Kinase

MEF:

Mouse Embryonic Fibroblast

MMPs:

Matrix Metalloproteinases

MSC:

Mesenchymal Stem Cells

Nes+:

Nestin Positive

NO:

Nitric Oxide

PGC:

Primordial Germ Cell

PM:

Peritubular Macrophage

PMC:

Peritubular Myoid Cell

PN:

Postnatal

PPAR-γ:

Proliferator-Activated Receptor-γ

PPR:

Parathyroid hormone protein receptor

RA:

Retinoic acid

RET:

Receptor Tyrosine Kinase

Runx2hi:

Runx2 high

SC:

Sertoli Cell

SCF:

Stem Cell Factor (KIT ligand)

SFK:

Src Family Kinase

SSC:

Spermatogonial Stem Cell

STO:

SIM mouse embryo-derived thioquanine – and- quabian –resistant cells

TJ:

Tight Junction

TPO:

Thrombopoietin

VE:

Vascular Endothelial

VEGF:

Vascular Endothelial Growth Factor

VEGFR2:

Vascular Endothelial Growth Factor Receptor-2

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Correspondence to Petek Korkusuz .

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Köse, S., Yersal, N., Önen, S., Korkusuz, P. (2018). Comparison of Hematopoietic and Spermatogonial Stem Cell Niches from the Regenerative Medicine Aspect. In: Turksen, K. (eds) Cell Biology and Translational Medicine, Volume 3. Advances in Experimental Medicine and Biology(), vol 1107. Springer, Cham. https://doi.org/10.1007/5584_2018_217

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